MONOSODIUM GLUTAMATE
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
Accent Ajinomoto alpha-Monosodium glutamate Anhydrous monosodium glutamate Chinese Seasoning E621 Glutacyl Glutamic acid, monosodium salt, L-(+)- MSG Natrii Glutamas RL-50 Sodium Glutamate Sodium hydrogen L-(+)-2-aminoglutarate monohydrate Vetsin Zest Chinese restaurant syndrome MSG (Monosodium glutamate) Sodium hydrogen L (+) alpha amino glutamate
IDENTIFIERS
USES/FORMS/SOURCES
MSG has the ability to increase salivation (HSDB, 2003). It has been used for many years as a flavor enhancer for a variety of foods such as Asian cuisines, canned vegetables, soups, and processed meats (Anon, 2003; HSDB, 2003). It has been estimated that the average daily intake of MSG is 0.3 to 1.0 grams in industrialized countries(Geha et al, 2000; Prawirohardjone et al, 2000). MSG has been used to treat patients with hyperammonemia in conditions such as hepatic encephalopathy. In the US, MSG has been used as a swine feed additive(HSDB, 2003).
In the grocery stores, MSG is sold as a fine, white crystal substance, similar in appearance to salt or sugar (Anon, 1995). LABEL LISTING: Foods and ingredients that contain glutamate as an inherent component (tomatoes, cheeses, meats, hydrolyzed protein products such as soy sauce, and autolyzed yeast extracts) are not required to list glutamate on the label. These ingredients are declared on the label by their common names. However, when MSG is added to food, the FDA requires "monosodium glutamate" to appear on the label. Other salts of glutamic acid (monopotassium glutamate, monoammonium glutamate) also have to be listed on labels and cannot appear under "spices", "natural flavoring", or other general terms (Anon, 2003). Anhydrous monosodium glutamate 29 grams or glutamic acid 25 grams is approximately equivalent to monosodium glutamate 32 grams (Sweetman, 2003).
Glutamate, a major building block of proteins, is released during breakdown of a protein molecule, and occurs naturally in many foods (eg; meat, milk, mushrooms, Parmesan cheese, and tomatoes) (Anon, 2003). Monosodium glutamate (MSG) is the monosodium salt of L-glutamic acid. It is produced by (HSDB, 2003; Anon, 2003): Fermentation of carbohydrate sources such as sugar beet molasses. Hydrolysis of vegetable proteins. Waste from beet-sugar molasses by acid hydrolysis. By action of Micrococcus glutamicus upon a carbohydrate and subsequent partial neutralization.
To produce MSG, sugar beet products are mainly used in the US and in Europe; other carbohydrate sources (eg, sugar cane and tapioca) are often used in the Orient (HSDB, 2003). OCCUPATIONAL EXPOSURE: Dermal contact or inhalation of dusts at places where MSG is produced or used(HSDB, 2003). NON-OCCUPATIONAL EXPOSURE: Ingestion of MSG-containing foods (HSDB, 2003).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: Monosodium glutamate (MSG) has the ability to increase salivation. It has been used as a flavor enhancer for a variety of foods such as Asian cuisines, canned vegetables, soups, and processed meats. It has also been used to treat patients with hyperammonemia in conditions such as hepatic encephalopathy. It has been estimated that the average daily intake of MSG is 0.3 to 1 g in industrialized countries.
- DESCRIPTION: Glutamic acid, or glutamate, is a major "building block" of many proteins in foods, such as cheese, meat, pea, mushrooms, and milk. MSG is the monosodium salt of L-glutamic acid. Some glutamate is present in foods in a "free" form, not bound with other amino acids. It is only in this free form that glutamate can enhance a food's flavor. Part of the flavor-enhancing effect of tomatoes, certain cheeses, and fermented or hydrolyzed protein products is due to the presence of free glutamate.
- TOXICOLOGY: MSG SYMPTOM COMPLEX OR CHINESE RESTAURANT SYNDROME (CRS): Although several mechanisms have been proposed to explain CRS, none have been proven. Some of the following proposed mechanisms are listed: (1) The stimulation of peripheral receptors. (2) CRS was a form of acetylcholinosis: In one study, it was noted that the symptoms of CRS were similar to those observed after acetylcholine use. Glutamate can be converted to acetylcholine via the tricarboxylic acid (TCA) cycle, and drugs affecting the cholinergic mechanisms could modulate CRS symptoms. (3) CRS may be a manifestation of esophageal irritation. (4) Chinese meals increase plasma sodium levels, causing CRS. (5) Vitamin B6 deficiency in individuals may cause CRS. (6) CRS may be caused by histamine; In one study, it was found that some Chinese meals could contain levels of histamine close to the toxic threshold established by the FDA for histamine in foods.
- EPIDEMIOLOGY: Exposure is common. Severe toxicity is rare.
MSG SYMPTOM COMPLEX OR CHINESE RESTAURANT SYNDROME: Following the consumption of a meal with MSG, patients have reported one or more symptoms of a complex which includes headache, nausea, vomiting, abdominal pain, weakness, dizziness, syncope, flushing, tingling, lacrimation, sweating, tightness of face and neck, burning or pressure in the chest often radiating to the neck and arms, heartburn, and gastric distress. Supraventricular and ventricular tachycardia have also been reported. However, there is inadequate data to determine if MSG may have been a factor.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
- Gastrointestinal decontamination is generally not indicated after an acute ingestion. Toxicity is very unlikely.
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
- Flushing, facial pressure, chest pain, headache, and nausea have been reported in patients following the ingestion of food containing MSG. Patients usually experience these symptoms within an hour of eating 3 g or more of MSG on an empty stomach (Sweetman, 2003).
- In one study, very high oral doses of glutamate (147 g/day) given to adult humans as the sole source of nonessential nitrogen for 2 to 6 weeks was tolerated, with no neurological changes (Bazzano et al, 1970). In other studies, doses 60 to 150 mg MSG/kg body weight were also tolerated (Geha et al, 2000).
- Carcinogenicity Ratings for CAS142-47-2 :
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 CAS142-47-2 (U.S. Environmental Protection Agency, 2011):
LD50- (INTRAPERITONEAL)RAT: LD50- (INTRAVENOUS)RAT: 3300 mg/kg (Sense Organs and Special Senses (Nose, Eye, Ear, and Taste); Autonomic Nervous System - Other (direct) parasympathomimetic; Behavioral - Ataxia) (RTECS, 2003)
LD50- (ORAL)RAT: LD50- (SUBCUTANEOUS)RAT: 5580 mg/kg (Behavioral - Tremor; Behavioral - Ataxia; Lung, Thorax, or Respiration - Cyanosis) (RTECS, 2003)
LD50- (INTRAPERITONEAL)MOUSE: LD50- (INTRAVENOUS)MOUSE: LD50- (ORAL)MOUSE: LD50- (SUBCUTANEOUS)MOUSE:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS142-47-2 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS142-47-2 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS142-47-2 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS142-47-2 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS142-47-2 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS142-47-2 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS142-47-2 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS142-47-2 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS142-47-2 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS142-47-2 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS142-47-2 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS142-47-2 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS142-47-2 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 142-47-2.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS142-47-2 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS142-47-2 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS142-47-2 (AIHA, 2006):
- DOE TEEL Values for CAS142-47-2 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS142-47-2 (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; 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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 CAS142-47-2 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
MOLECULAR WEIGHT
DESCRIPTION/PHYSICAL STATE
- White, practically odorless, free-flowing crystals or crystalline powder; sweet-saline taste in large concentrations; no flavor in small quantity; freely soluble in water; sparingly soluble in alcohol (HSDB, 2003; Sweetman, 2003).
-REFERENCES
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