GLYCOLIC ACID
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
IDENTIFIERS
SYNONYM REFERENCE
- (HSDB , 2002; RTECS , 2002)
USES/FORMS/SOURCES
Glycolic acid has a variety of uses in several industries, primarily in pH control or where an inexpensive organic acid is needed. It does not tend to cause corrosion and has bactericidal properties, leading to its common use in acidic cleansing agents. For example, it is an ingredient of dairy and industrial cleaning agents. It inhibits the growth of iron-oxidizing bacteria, in particular. Glycolic acid is also used as a water treatment agent and for rust and scale removal in heat exchangers and pipelines (Ashford, 2001; Budavari, 2001; HSDB , 2002; ILO, 1998). Glycolic acid is an effective complexing agent, contributing to its wide use in the metals industry. It is used in the processing of metals, such as pickling, cleaning, and chemical milling; in polishing and soldering compounds; in the preparation of electroplating and galvanizing baths; as an etching agent for lithographic plates; as an aluminum anodizing reagent; as a copperplating brightening agent; and as a nickel-hydrazine coating reagent. It is also used in the textile industry in textile dyeing, printing and creaseproofing and in fur-processing operations. Glycolic acid's use in the tanning industry is as an auxiliary in leather tanning and in leather dyeing operations (Ashford, 2001; Budavari, 2001; ILO, 1998; Lewis, 2001a). Other uses include in adhesives, for breaking of petroleum emulsions, and as a chelating agent. The metal ion complexing ability is useful in dissolution of hard water scale and prevention of deposition. It is used to chelate calcium (II) and to delime hides in leather processing. It is also included in alum and chrome mordants for dye fixing. It is a skin-conditioning additive in cosmetics, serving as a humectant to help the skin retain moisture. It may be used for medication purposes as well (Ashford, 2001; (Dupont, 1997); HSDB , 2002; ITI, 1995; Lewis, 2001a). In the past, glycolic acid was a regulated antimicrobial pesticide under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). Its use as a pesticide has been cancelled, however. HSDB (2002) reports that no products containing the glycolic acid pesticide are actively registered. However, glycolic acid remains regulated by FIFRA because EPA identifies it as an inert ingredient under FIFRA. It is included in the toxicological category List 3, inerts of unknown toxicity. The EPA's Office of Pesticide Programs (OPP) assigned a PC code to glycolic acid of 000101. It is currently an ingredient of a few active products according to the USEPA/OPP Pesticide Products Database ((EPA, 2002); (EPA, 2000); HSDB , 2002).
Glycolic acid is an organic acid. Pure glycolic acid is a deliquescent crystalline solid. The crystals may be somewhat hygroscopic, tending to undergo gradual dissolution by the absorption of moisture from the air. The crystals are odorless and colorless (Budavari, 2001; ILO, 1998; Lewis, 2001a). It occurs as rhombic needles from water, as leaves from ethanol, or as rhombic leaflets from ether (HSDB , 2002; ILO, 1998; Lewis, 2000a). Glycolic acid is commercially available as a technical grade 70% aqueous solution, as a 57% aqueous solution, or as 100% crystalline solid. The liquid has a straw-type color and an odor similar to burnt sugar (Ashford, 2001; ITI, 1995; HSDB , 2002; Lewis, 2001a).
Glycolic acid can be derived from chloroacetic acid by a hydration reaction with sodium hydroxide or by reduction of oxalic acid. It is an intermediate in the production of ethylene glycol. It is also a naturally occurring constituent of sugar cane syrup (Ashford, 2001; Budavari, 2001; HSDB , 2002; Lewis, 2001a). It is produced from carbonylation of formaldehyde and carbon monoxide. Under high pressure, formaldehyde reacts with CO and water in the presence of an acid catalyst to form hydroxyacetic acid (Ashford, 2001; HSDB , 2002). Glycolic acid is manufactured by (HSDB , 2002): Hydrolysis of glyconitrile with an acid such as phosphite or sulphite at 100-150 degrees C. Water hydrolysis of trichloroethylene under pressure at 150 degrees C. Treatment of glycine with nitric acid. Oxidation of hexoses, isoamyl benzoate, and 5-oxodigluconic acid. Treatment of trioxymethylene with carbon monoxide and water in the presence of catalysts at greater than 30MPa.
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
Glycolic acid is irritating to mucous membranes. Rats exposed over two weeks to various air concentrations experienced hepatic damage and distension of the gastrointestinal tract, spleen and thymus.
Pure glycolic acid is moderately toxic by ingestion. Based on animal data, the 70% solution is slightly toxic by the oral route. The oral LD50 for rats is 1938 mg/kg and 1920 mg/kg for guinea pigs. A repeated dose, 90-day rat gavage study found decreased body weight and weight gain. Male rats showed toxicologically significant changes in hematologic measurements (increased neutrophils), clinical chemistries, and urinalysis parameters with kidney lesions. Corresponding findings were not observed in females.
Glycolic acid is a severe skin and eye irritant. The 70% solution can cause chemical eye and dermal burns. Irritant effects are concentration dependent as these effects are markedly reduced with the 20% solution. Glycolic acid is a common component of personal care products and is used in the treatment of skin disorders. Systemic absorption is possible following dermal exposure. Dermal absorption over 24 hours ranges from about 30% to 3% of the quantity applied for products ranging from pH 3 to 7, respectively. Irritation at the application site has been observed, but systemic toxicity has not been associated with these types of applictions. Toxicity studies on products formulated and used within recommended pH limits and concentrations have been found safe for personal care use. One human study looked at the application of a 70% glycolic acid solution on sun-damaged skin for 30 minutes. Biopsies showed partial epidermal necrosis and epidermal crusting at pH 0.6, epidermal crusting at pH 1.8, and partial loss of stratum corneum at pH 2.25 and 2.75. Application of 50% solution (pH 1.0) showed loss of stratum corneum, but no crusting or epidermal necrosis. Numerous human studies with cosmetic products containing low concentrations of glycolic acid have been completed. No corrosivity was observed at the low concentrations. It is not a skin sensitizer in animals. Moderately severe injury, grade 7 on a 1 to 10 scale, was reported with a 24-hour drip test of aqueous solution on rabbit eyes.
- EFFECTS OF CHRONIC EXPOSURE
Cumulative exposure effects of glycolic acid are not known. It is believed to be metabolized to glycine. Glycolic acid is a metabolite of ethylene glycol, causing acidosis, the characteristic toxic effect of ethylene glycol poisoning.
- POTENTIAL HEALTH HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
-MEDICAL TREATMENT
LIFE SUPPORT
- Support respiratory and cardiovascular function.
SUMMARY
- FIRST AID - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves.
INHALATION EXPOSURE - INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm.
DERMAL EXPOSURE - EYE EXPOSURE - DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
ORAL EXPOSURE - Because of the potential for gastrointestinal tract irritation, DO NOT induce emesis. DILUTION: If no respiratory compromise is present, administer milk or water as soon as possible after ingestion. Dilution may only be helpful if performed in the first seconds to minutes after ingestion. The ideal amount is unknown; no more than 8 ounces (240 mL) in adults and 4 ounces (120 mL) in children is recommended to minimize the risk of vomiting.
-RANGE OF TOXICITY
MINIMUM LETHAL EXPOSURE
A number of rats died within 8 hours of a 5-6 g/kg body weight dose of glycolic acid (HSDB , 2002). Repeated dose toxicity was evaluated in a 90-day gavage study on rats. Dosages were administered daily at 0, 150, 300, and 600 mg/kg in water via intragastric intubation. Two compound-relates deaths were reported at the 600 mg/kg glycolic acid dose level ((Dupont, 2002)).
MAXIMUM TOLERATED EXPOSURE
Repeated dose toxicity was evaluated in a 90-day gavage study on rats. Dosages were administered daily at 0, 150, 300, and 600 mg/kg in water via intragastric intubation. Effects on body weight, food consumption, or clinical signs were not observed at the 150 mg/kg glycolic acid dose level. In addition, there were no adverse clinical signs indicative of systemic toxicity observed during the study ((Dupont, 2002)). A two-week inhalation study evaluating repeated dose toxicity was performed on rats at exposure levels of 0.16, 0.51, and 1.4 mg/l glycolic acid for 6 hours per day, five times a week. There were no test substance related clinical pathology changes in the 0.16 mg/L dose level group. This level was considered a no adverse effect level, as the only effect observed at this level was a very mild, diffuse hepatocellular degeneration in one of ten rats 14 days post-exposure ((Dupont, 2002)).
CARCINOGENICITY- The NTP is currently evaluating glycolic acid in a long-term study to determine the toxicologic and/or carcinogenic effects of long-term exposure. The laboratory study report is in preparation. The study details are as follows (HSDB , 2002; NTP , 2002): NTP Management Status Report - Progress of 2-week, 13-week, and 2-year Toxicology and Carcinogenesis Studies, Ref. No. 8, Long-Term Exposure Studies: Laboratory Study Report in Preparation CHEMICAL NAME: Alpha/Beta Hydroxy Acids (Glycolic Acid): Glycolic Acid; Hydroxyacetic Acid (9CI); Glycolic Acid (Alph/Beta Hydroxy Acids) CAS Number: 79-14-1 USE: COSM/N/S (Cosmetics, Perfumes, Fragrances, Hair Preparations, Skin Lotions/Naturally Occurring and Synthetic) ROUTE: SP (Topical) SPECIES: MT (mice: skh-1 hairless) ADDITIONAL DETAIL: 52 weeks, histopathology
- Carcinogenicity Ratings for CAS79-14-1 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS79-14-1 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS79-14-1 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS79-14-1 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS79-14-1 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS79-14-1 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS79-14-1 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS79-14-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS79-14-1 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS79-14-1 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS79-14-1 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS79-14-1 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS79-14-1 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS79-14-1 (EPA, 2005):
SHIPPING REGULATIONS
- DOT -- Table of Hazardous Materials and Special Provisions for UN/NA Number 2811 (49 CFR 172.101, 2005):
Hazardous materials descriptions and proper shipping name: Toxic solids, organic, n.o.s Symbol(s): G Hazard class or Division: 6.1 Identification Number: UN2811 Packing Group: I Label(s) required (if not excepted): 6.1 Special Provisions: IB7, T6, TP33 IB7: Authorized IBCs: Metal (11A, 11B, 11N, 21A, 21B, 21N, 31A, 31B and 31N); Rigid plastics (11H1, 11H2, 21H1, 21H2, 31H1 and 31H2); Composite (11HZ1, 11HZ2, 21HZ1, 21HZ2, 31HZ1 and 31HZ2); Wooden (11C, 11D and 11F). Additional Requirement: Liners of wooden IBCs must be sift-proof. T6: Minimum test pressure (bar): 4; Minimum shell thickness (in mm-reference steel) (See sxn.178.274(d)): sxn.178.274(d)(2); Pressure-relief requirements (See sxn.178.275(g)): Normal; Bottom opening requirements (See sxn.178.275(d)): sxn.178.275(d)(2). TP33: The portable tank instruction assigned for this substance applies for granular and powdered solids and for solids which are filled and discharged at temperatures above their melting point which are cooled and transported as a solid mass. Solid substances transported or offered for transport above their melting point are authorized for transportation in portable tanks conforming to the provisions of portable tank instruction T4 for solid substances of packing group III or T7 for solid substances of packing group II, unless a tank with more stringent requirements for minimum shell thickness, maximum allowable working pressure, pressure-relief devices or bottom outlets are assigned in which case the more stringent tank instruction and special provisions shall apply. Filling limits must be in accordance with portable tank special provision TP3. Solids meeting the defnintion of an elevated temperature material must be transported in accordance with the applicable requirements of this subchapter.
Packaging Authorizations (refer to 49 CFR 173.***): Exceptions: None Non-bulk packaging: 211 Bulk packaging: 242
Quantity Limitations: Vessel Stowage Requirements:
Hazardous materials descriptions and proper shipping name: Toxic solids, organic, n.o.s Symbol(s): Not Listed Hazard class or Division: 6.1 Identification Number: UN2811 Packing Group: II Label(s) required (if not excepted): 6.1 Special Provisions: IB8, IP2, IP4, T3, TP33 IB8: Authorized IBCs: Metal (11A, 11B, 11N, 21A, 21B, 21N, 31A, 31B and 31N); Rigid plastics (11H1, 11H2, 21H1, 21H2, 31H1 and 31H2); Composite (11HZ1, 11HZ2, 21HZ1, 21HZ2, 31HZ1 and 31HZ2); Fiberboard (11G); Wooden (11C, 11D and 11F); Flexible (13H1, 13H2, 13H3, 13H4, 13H5, 13L1, 13L2, 13L3, 13L4, 13M1 or 13M2). IP2: When IBCs other than metal or rigid plastics IBCs are used, they must be offered for transportation in a closed freight container or a closed transport vehicle. IP4: Flexible, fiberboard or wooden IBCs must be sift-proof and water-resistant or be fitted with a sift-proof and water-resistant liner. T3: Minimum test pressure (bar): 2.65; Minimum shell thickness (in mm-reference steel) (See sxn.178.274(d)): sxn.178.274(d)(2); Pressure-relief requirements (See sxn.178.275(g)): Normal; Bottom opening requirements (See sxn.178.275(d)): sxn.178.275(d)(2). TP33: The portable tank instruction assigned for this substance applies for granular and powdered solids and for solids which are filled and discharged at temperatures above their melting point which are cooled and transported as a solid mass. Solid substances transported or offered for transport above their melting point are authorized for transportation in portable tanks conforming to the provisions of portable tank instruction T4 for solid substances of packing group III or T7 for solid substances of packing group II, unless a tank with more stringent requirements for minimum shell thickness, maximum allowable working pressure, pressure-relief devices or bottom outlets are assigned in which case the more stringent tank instruction and special provisions shall apply. Filling limits must be in accordance with portable tank special provision TP3. Solids meeting the defnintion of an elevated temperature material must be transported in accordance with the applicable requirements of this subchapter.
Packaging Authorizations (refer to 49 CFR 173.***): Exceptions: 153 Non-bulk packaging: 212 Bulk packaging: 242
Quantity Limitations: Vessel Stowage Requirements:
Hazardous materials descriptions and proper shipping name: Toxic solids, organic, n.o.s Symbol(s): Not Listed Hazard class or Division: 6.1 Identification Number: UN2811 Packing Group: III Label(s) required (if not excepted): 6.1 Special Provisions: IB8, IP3, T1, TP33 IB8: Authorized IBCs: Metal (11A, 11B, 11N, 21A, 21B, 21N, 31A, 31B and 31N); Rigid plastics (11H1, 11H2, 21H1, 21H2, 31H1 and 31H2); Composite (11HZ1, 11HZ2, 21HZ1, 21HZ2, 31HZ1 and 31HZ2); Fiberboard (11G); Wooden (11C, 11D and 11F); Flexible (13H1, 13H2, 13H3, 13H4, 13H5, 13L1, 13L2, 13L3, 13L4, 13M1 or 13M2). IP3: Flexible IBCs must be sift-proof and water-resistant or must be fitted with a sift-proof and water-resistant liner. T1: Minimum test pressure (bar): 1.5; Minimum shell thickness (in mm-reference steel) (See sxn.178.274(d)): sxn.178.274(d)(2); Pressure-relief requirements (See sxn.178.275(g)): Normal; Bottom opening requirements (See sxn.178.275(d)): sxn.178.275(d)(2). TP33: The portable tank instruction assigned for this substance applies for granular and powdered solids and for solids which are filled and discharged at temperatures above their melting point which are cooled and transported as a solid mass. Solid substances transported or offered for transport above their melting point are authorized for transportation in portable tanks conforming to the provisions of portable tank instruction T4 for solid substances of packing group III or T7 for solid substances of packing group II, unless a tank with more stringent requirements for minimum shell thickness, maximum allowable working pressure, pressure-relief devices or bottom outlets are assigned in which case the more stringent tank instruction and special provisions shall apply. Filling limits must be in accordance with portable tank special provision TP3. Solids meeting the defnintion of an elevated temperature material must be transported in accordance with the applicable requirements of this subchapter.
Packaging Authorizations (refer to 49 CFR 173.***): Exceptions: 153 Non-bulk packaging: 213 Bulk packaging: 240
Quantity Limitations: Vessel Stowage Requirements:
- ICAO International Shipping Name for UN2811 (ICAO, 2002):
LABELS
- NFPA Hazard Ratings for CAS79-14-1 (NFPA, 2002):
-HANDLING AND STORAGE
SUMMARY
Glycolic acid may be in the pure solid crystalline form or in the form of an aqueous solution. Strict precautions should be used during handling of glycolic acid, because it can produce severe chemical burns of the skin and eyes. It is stronger than acetic acid. Personal protective equipment should be used that is appropriate to the chemical form and concentration. At a minimum, rubber gloves and eye protection should be used to prevent skin and eye contact. Container storage of glycolic acid solution may be in plastic drums, glass containers, or stainless steel tanks. The solid may be in fiber drums (Ashford, 2001; Budavari, 2001; (Dupont, 1997); ILO , 1998; ITI, 1995; HSDB , 2002; Lewis, 2001).
HANDLING
- Because glycolic acid can cause very severe chemical burns to the skin and eyes and because it is irritating to the mucous membranes, strict precautions should be instituted for its handling. Personal protective equipment should be worn when handling concentrated solutions. During routine handling of glycolic acid, rubber gloves and splash goggles are recommended ((Dupont, 1997); ILO , 1998; Lewis, 2000).
STORAGE
Containers of glycolic acid solution may be supplied in 55-gallon polyethylene drums or 5-gallon pails. Bulk solution is transported in 304 or 316 stainless steel tanks. Solid material is supplied in fiber drums. Polymeric materials such as polypropylene, PVC, epoxy, vinyl ester, and polyethylene are stable to glycolic acid, depending on the concentration and temperature. Containers storage should consider that glycolic acid is mildly corrosive to iron, mild steel, tin, and aluminum at ambient temperatures ((Dupont, 1997)). Containers for acids should be glass or stainless steel. Proper labeling of containers during storage and transport is also recommended (ILO , 1998).
- ROOM/CABINET RECOMMENDATIONS
Containers should be stored upright in an area protected from rain, moving equipment and vehicles. The storage area should be maintained at a temperature above 10 degrees C (50 degrees F), in order to prevent precipitation of glycolic acid crystals ((Dupont, 1997)). Storage of all types of acids should be maintained away from ignition sources and oxidizing materials. Storage areas should be well ventilated to prevent accumulation of dangerous levels of vapors (ILO , 1998).
Glycolic acid is incompatible with sulfuric acid, caustics, ammonia, aliphatic amines, isocyanates, alkylene oxides, epichlorohydrin, and strong oxidizers. Solid glycolic acid in contact with active metals may produce flammable hydrogen gas ((Dupont, 2002); Pohanish & Greene, 1997). Glycolic acid is mildly corrosive to iron, mild steel, tin, and aluminum at ambient temperatures. Copper and bronze will be not be resistant to the corrosive action of glycolic acid in the presence of air ((Dupont, 1997)).
-PERSONAL PROTECTION
SUMMARY
- RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
- Because glycolic acid is a skin and eye irritant and may cause severe chemical burns in concentrated form, personal protective equipment such as rubber gloves, protective clothing, goggles, or a face shield should be utilized when handling concentrated solutions or other forms of glycolic acid. A body shield and self-contained breathing apparatus (SCBA) may also be used. Acrid smoke and irritating fumes are released when glycolic acid is heated to decomposition. As a result, inhalation exposure should be avoided through the use of respiratory protection when solutions are boiled or in instances of fire where glycolic acid is involved (ILO , 1998; ITI, 1995; Lewis, 2000).
EYE/FACE PROTECTION
- Proper eye protection, such as a face shield or chemical splash goggles, should be used when handling this material due to the contact hazard and risk of chemical burns ((Dupont, 1997); ILO , 1998; ITI, 1995).
RESPIRATORY PROTECTION
- Acrid smoke and irritating fumes are released when glycolic acid is heated to decomposition. Inhalation exposure should be avoided through the use of respiratory protection when the material is boiled or in instances of fire. Personal protective equipment may include use of a SCBA (ILO , 1998; ITI, 1995; Lewis, 2000).
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 79-14-1.
ENGINEERING CONTROLS
- Process enclosures, local exhaust ventilation, or other engineering controls should be used to limit dust concentrations (DOLPHIN , 2002).
-PHYSICAL HAZARDS
FIRE HAZARD
POTENTIAL FIRE OR EXPLOSION HAZARDS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004) Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
Glycolic acid in its solid form is a combustible substance. It will emit acrid smoke and irritating fumes when heated to decomposition. Contact of solid glycolic acid material with active metals may produce flammable hydrogen gas. Inhalation exposure should be avoided through the use of respiratory protection in a fire involving glycolic acid because acrid smoke and irritating fumes are released when it is heated to decomposition ((Dupont, 2002); ILO , 1998; ITI, 1995; Lewis, 2000; Lewis, 2001). Aqueous solutions of glycolic acid at 70% solution are nonflammable ((Dupont, 1997)).
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS79-14-1 (NFPA, 2002):
- INITIATING OR CONTRIBUTING PROPERTIES
- FIRE CONTROL/EXTINGUISHING AGENTS
- SMALL FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
- LARGE FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
Dry chemical, CO2, alcohol-resistant foam or water spray. Move containers from fire area if you can do it without risk. Dike fire control water for later disposal; do not scatter the material.
- TANK OR CAR/TRAILER LOAD FIRE PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
Fight fire from maximum distance or use unmanned hose holders or monitor nozzles. Do not get water inside containers. Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.
- NFPA Extinguishing Methods for CAS79-14-1 (NFPA, 2002):
- Water spray, dry chemical, or carbon dioxide are suitable extinguishing agents for a fire involving glycolic acid (DOLPHIN , 2002).
EXPLOSION HAZARD
- Dust explosion can occur when the solid material is at an adequate airborne concentration and of a reduced particle size (DOLPHIN , 2002).
DUST/VAPOR HAZARD
- Glycolic acid may create a dust explosion at a sufficient airborne concentration and at a reduced particle size (DOLPHIN , 2002).
REACTIVITY HAZARD
- Glycolic acid is incompatible with sulfuric acid, caustics, ammonia, aliphatic amines, isocyanates, alkylene oxides, epichlorohydrin, and strong oxidizers (Pohanish & Greene, 1997).
EVACUATION PROCEDURES
- Initial Isolation and Protective Action Distances (ERG, 2004)
Data presented from the Emergency Response Guidebook Table of Initial Isolation and Protective Action Distances are for use when a spill has occurred and there is no fire. If there is a fire, or if a fire is involved, evacuation information presented under FIRE - PUBLIC SAFETY EVACUATION DISTANCES should be used. Generally, a small spill is one that involves a single, small package such as a drum containing up to approximately 200 liters, a small cylinder, or a small leak from a large package. A large spill is one that involves a spill from a large package, or multiple spills from many small packages. Suggested distances to protect from vapors of toxic-by-inhalation and/or water-reactive materials during the first 30 minutes following the spill.
- SPILL - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
Increase, in the downwind direction, as necessary, the isolation distance of at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids in all directions.
- FIRE - PUBLIC SAFETY EVACUATION DISTANCES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.
- PUBLIC SAFETY MEASURES - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004)
CALL Emergency Response Telephone Number on Shipping Paper first. If Shipping Paper not available or no answer, refer to appropriate telephone number: MEXICO: SETIQ: 01-800-00-214-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5559-1588; For calls originating elsewhere, call: 011-52-555-559-1588.
CENACOM: 01-800-00-413-00 in the Mexican Republic; For calls originating in Mexico City and the Metropolitan Area: 5550-1496, 5550-1552, 5550-1485, or 5550-4885; For calls originating elsewhere, call: 011-52-555-550-1496, or 011-52-555-550-1552; 011-52-555-550-1485, or 011-52-555-550-4885.
ARGENTINA: CIQUIME: 0-800-222-2933 in the Republic of Argentina; For calls originating elsewhere, call: +54-11-4613-1100.
BRAZIL: PRÓ-QUÍMICA: 0-800-118270 (Toll-free in Brazil); For calls originating elsewhere, call: +55-11-232-1144 (Collect calls are accepted).
COLUMBIA: CISPROQUIM: 01-800-091-6012 in Colombia; For calls originating in Bogotá, Colombia, call: 288-6012; For calls originating elsewhere, call: 011-57-1-288-6012.
CANADA: UNITED STATES:
For additional details see the section entitled "WHO TO CALL FOR ASSISTANCE" under the ERG Instructions. As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas.
- AIHA ERPG Values for CAS79-14-1 (AIHA, 2006):
- DOE TEEL Values for CAS79-14-1 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Glycolic acid; (Hydroxyacetic acid) TEEL-0 (units = mg/m3): 75 TEEL-1 (units = mg/m3): 250 TEEL-2 (units = mg/m3): 500 TEEL-3 (units = mg/m3): 500 Definitions: TEEL-0: The threshold concentration below which most people will experience no adverse health effects. TEEL-1: The airborne concentration (expressed as ppm [parts per million] or mg/m(3) [milligrams per cubic meter]) of a substance above which it is predicted that the general population, including susceptible individuals, could experience notable discomfort, irritation, or certain asymptomatic, nonsensory effects. However, these effects are not disabling and are transient and reversible upon cessation of exposure. TEEL-2: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience irreversible or other serious, long-lasting, adverse health effects or an impaired ability to escape. TEEL-3: The airborne concentration (expressed as ppm or mg/m(3)) of a substance above which it is predicted that the general population, including susceptible individuals, could experience life-threatening adverse health effects or death.
- AEGL Values for CAS79-14-1 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2009; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS79-14-1 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
SPILL OR LEAK PRECAUTIONS - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004) ELIMINATE all ignition sources (no smoking, flares, sparks or flames in immediate area). Do not touch damaged containers or spilled material unless wearing appropriate protective clothing. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers. DO NOT GET WATER INSIDE CONTAINERS.
RECOMMENDED PROTECTIVE CLOTHING - EMERGENCY RESPONSE GUIDEBOOK, GUIDE 154 (ERG, 2004) Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible.
Spills of glycolic acid can be covered with soda ash or sodium bicarbonate. Mixing this material with water, neutralization can be accomplished for safe disposition (ITI, 1995).
Glycolic acid can be neutralized for safe disposition using soda ash or sodium bicarbonate and water (ITI, 1995). Waste management activities associated with material disposition are unique to individual situations. Proper waste characterization and decisions regarding waste management should be coordinated with the appropriate local, state, or federal authorities to ensure compliance with all applicable rules and regulations.
-ENVIRONMENTAL HAZARD MANAGEMENT
POLLUTION HAZARD
- The total worldwide annual consumption of glycolic acid solution has been reported as approximately 2,000-3,000 tons of solution. The annual U.S. market is 25-30 million pounds, which is primarily supplied by domestic production. Imports account for approximately 5% of sales ((Dupont, 1997); HSDB , 2002).
- A source of glycolic acid that could contribute to environmental releases is the spent sulfite liquor resulting from pulp processing (HSDB , 2002).
- Glycolic acid appears in food as an indirect additive due to its use in adhesives (HSDB , 2002).
- Glycolic acid is naturally occurring in fruits, vegetables, meats, and beverages in concentrations ranging from approximately 0.5-5.6 mg/100 mg (vegetables), approximately 5-50 mg/kg (fruits), 1-5 mg/kg (beef and chicken), and approximately 0.5-30 mg/kg (common non-alcoholic beverages) ((Dupont, 2002)).
ENVIRONMENTAL FATE AND KINETICS
SURFACE WATER If released to water, glycolic acid will remain in the water phase and undergo biodegradation and possibly photodegradation. Acclimation is not an important factor in the rate of biodegradation, based on data that used a variety of inoculum. Bioaccumulation and persistence are not expected. It does not rapidly volatilize based on the estimated Henry's Law constant of 8.5 x 10 (-8) atm-m(3)/mole ((Dupont, 2002)).
OTHER The half-life from a model river 1 m deep, flowing 1 m/sec, and with a wind velocity of 3 m/sec, was estimated to be 373.8 days ((Dupont, 2002)). Estimated half-life of gylcolic acid in a model lake 1 m deep, flowing 0.05 m/sec, and with a wind velocity of 0.5 m/sec, is 2721 days. This estimate is based on volatilization and does not account for biodegradation ((Dupont, 2002)).
ABIOTIC DEGRADATION
- Photodegradation by photolysis in water was reported in a study that used a calculated light spectrum of 240-300 nm on a concentration of 100 mmol/L glycolic acid at 25 degrees C. Twenty percent degradation occurred after 90 minutes ((Dupont, 2002)).
BIODEGRADATION
- Glycolic acid has been found to be readily biodegradable. Nearly 90% biodegradation was observed after 7 days in laboratory testing using the Closed Bottle Test ((Dupont, 2002)).
BIOACCUMULATION
AQUATIC Glycolic acid is not expected to bioaccumulate in the environment ((Dupont, 2002)). Glycolic acid is not expected to bioaccumulate in the environment ((Dupont, 2002)).
ENVIRONMENTAL TOXICITY
- EC50 - DAPHNIA MAGNA (WATER): 141 mg/l (48 hour) (Dupont, 2002)
- LC50 - FATHEAD MINNOW (Pimephales promelas) (WATER): 164 ppm (96 hour) (Dupont, 2002)
- The effects on growth rate of Haematococcus pluvialis (algae) were evaluated in a study on the acute toxicity of glycolic acid to aquatic plants. Algal growth was stimulated at pH 7.5 under illumination. Glycolic acid did not support heterotrophic growth without light (pH 5 or 7.5, 14 day incubation period), but was an effective substrate for photoheterotrophic growth at pH 5 ((Dupont, 2002)).
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- Glycolic acid in its pure state is in the form of solid, colorless and odorless crystals. It may appear as rhombic needles from water or as leaves from ethanol or ether. The 70% aqueous solution of glycolic acid is a light, straw color and may have an odor similar to that of burnt sugar. The chemical does not tend to cause corrosion, and it will decompose upon boiling (Ashford, 2001; Lewis, 2000; Lewis, 2001).
PH
- AQUEOUS SOLUTION (Budavari, 2001):
VAPOR PRESSURE
- 8.1 mmHg (at 80 degrees C) (HSDB , 2002)
- Solid: 0.017 mmHg (at 25 degrees C) (extrapolated) ((Dupont, 2002))
SPECIFIC GRAVITY
- TEMPERATURE AND/OR PRESSURE NOT LISTED
DENSITY
- NORMAL TEMPERATURE AND PRESSURE
(25 degrees C; 77 degrees F and 760 mmHg) 1.49 kg/l (25 degrees C) (Ashford, 2001; HSDB , 2002)
- OTHER TEMPERATURE AND/OR PRESSURE
70% Solution: 1.25 g/cm(3) (at 26 degrees C) ((Dupont, 2002)) Solid: 1.36 g/cm(3) (at 26 degrees C) ((Dupont, 2002))
FREEZING/MELTING POINT
80 degrees C (Budavari, 2001; ILO , 1998) alpha: 63 degrees C (Verschueren, 2000; Lewis, 2000) beta: 79 degrees C (Verschueren, 2000; Lewis, 2000) 79 degrees C (Ashford, 2001) 70% Solution: 10 degrees C (Lewis, 2001) Solid: 78-79 degrees C (Lewis, 2001)
BOILING POINT
- Decomposes upon boiling (Verschueren, 2000; (Lewis, 2000)
- 100 degrees C with decomposition (Ashford, 2001; HSDB , 2002)
FLASH POINT
- Not applicable ((Dupont, 2002))
SOLUBILITY
Soluble (Ashford, 2001; Budavari, 2001; ILO , 1998; Lewis, 2000) Approximately 2440 g/kg H20 (>99% glycolic acid) (at 25 degrees C) ((Dupont, 2002))
Soluble in methanol, alcohol, acetone, acetic acid, and ether (Budavari, 2001; Lewis, 2000). Soluble in oxygenated solvents (Ashford, 2001).
OCTANOL/WATER PARTITION COEFFICIENT
- log Kow = -1.11 ((Dupont, 2002)) Verschueren, 2000)
HENRY'S CONSTANT
- 8.5 X 10 (-8) atm-m(3)/mole (estimated) ((Dupont, 2002))
SPECTRAL CONSTANTS
OTHER/PHYSICAL
- NUCLEAR MAGNETIC RESONANCE
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