PHENOLPHTHALEIN
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
PHENOLPHTHALEIN AGORAL 3,3-BIS(p-HYDROXYPHENYL)PHTHALIDE alpha-DI(p-HYDROXYPHENYL)PHTHALIDE DIHYDROXYPHTHALOPHENONE EUCHESSINA EVAC-Q-KIT EVAC-Q-KWIK EVAC-U-GEN FEEN-A-MINT GUM FENOLFTALEIN (Czech) 1(3H)-ISOBENZOFURANONE, 3,3-BIS(4-HYDROXYPHENYL)-KOPROL LAXOGEN LILO PHTHALIDE 3,3,-BIS(p-HYDROXYPHENYL)- PHTHALIMETTEN PRULET PURGA PURGEN PURGOPHEN SPULMAKO-LAX TRILAX
IDENTIFIERS
USES/FORMS/SOURCES
PHENOLPHTHALEIN is used as a pH indicator and in dyes, and also as a human and veterinary laxative (HSDB , 1998). Phenolphthalein for laxative use can be abused (De Wolff, 1983; Larusso & McGill, 1975). One case of daily doses for 20 years, including up to 12 doses per day for 2 to 3 years, has been reported (Watson, 1982).
PHENOLPHTHALEIN is usually a white or yellowish-white odorless crystalline solid which is almost insoluble in water, is slightly soluble in chloroform, somewhat soluble in alcohol (1 g/12 mL) and ether, and is soluble in acetone, pyridine, or dilute solutions of alkali hydroxide (HSDB , 1998; Budavari, 1996; Lewis, 1993). When in aqueous solution, phenolphthalein is a pH indicator and changes from colorless below pH 8.5 to deep red above pH 9 (HSDB , 1998; Budavari, 1996). As a laxative for human use, it is available in 60 and 120 mg tablets (HSDB , 1998).
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
ACUTE CLINICAL EFFECTS
When taken orally, phenolphthalein acts as a laxative with its action delayed by approximately 6 to 8 hours. Its mechanism of action is not completely understood, but it may directly stimulate the smooth muscle of the intestine (HSDB , 1998). Acute toxic effects by other routes of exposure have not been documented in humans, but severe ingestion poisonings have been reported (Buchanan et al, 1976; Sidhu et al, 1989). Fulminant hepatic failure and disseminated intravascular coagulation were seen in one overdose case (Sidhu et al, 1989). Phenolphthalein can induce free radicals and has estrogenic activity (Dunnick & Hailey, 1996).
Acute ingestion of therapeutic doses of phenolphthalein-containing laxatives has rarely been associated with the development of life-threatening toxic epidermal necrolysis (TEN) (Artymowicz et al, 1997; Kar et al, 1986).
CHRONIC CLINICAL EFFECTS
When abused as a laxative, it can cause depletion of electrolytes, irritation of the pancreas (Lambrianides & Rosin, 1984), gastrointestinal bleeding, anemia (Weiss & Wood, 1981), kidney failure (Watson, 1982), osteomalacia (Frame et al, 1971), and chronic diarrhea (Larusso & McGill, 1975).
The effects of chronic exposure to phenolphthalein involve its use as a laxative. The main concerns are ALLERGIC REACTIONS (involving swelling of the eyelids) and skin rashes (which can resemble systemic lupus erythematosus) (HSDB , 1998; Adkinson, 1977). It can cause fixed drug reactions (painful red skin macules) with intermittent therapeutic use (Stroud & Rosio, 1987) Wyatt et al, 1972).
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
- Carcinogenicity Ratings for CAS77-09-8 :
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): 2B ; Listed as: Phenolphthalein 2B : The agent (mixture) is possibly carcinogenic to humans. The exposure circumstance entails exposures that are possibly carcinogenic to humans. This category is used for agents, mixtures and exposure circumstances for which there is limited evidence of carcinogenicity in humans and less than sufficient evidence of carcinogenicity in experimental animals. It may also be used when there is inadequate evidence of carcinogenicity in humans but there is sufficient evidence of carcinogenicity in experimental animals. In some instances, an agent, mixture or exposure circumstance for which there is inadequate evidence of carcinogenicity in humans but limited evidence of carcinogenicity in experimental animals together with supporting evidence from other relevant data may be placed in this group.
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 CAS77-09-8 (U.S. Environmental Protection Agency, 2011):
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS77-09-8 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS77-09-8 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS77-09-8 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS77-09-8 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS77-09-8 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS77-09-8 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS77-09-8 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS77-09-8 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS77-09-8 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS77-09-8 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS77-09-8 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS77-09-8 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS77-09-8 (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 77-09-8.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS77-09-8 (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 CAS77-09-8 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS77-09-8 (AIHA, 2006):
- DOE TEEL Values for CAS77-09-8 (U.S. Department of Energy, Office of Emergency Management, 2010):
Listed as Phenolphthalein TEEL-0 (units = mg/m3): 0.75 TEEL-1 (units = mg/m3): 2.5 TEEL-2 (units = mg/m3): 15 TEEL-3 (units = mg/m3): 400 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 CAS77-09-8 (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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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; 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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 CAS77-09-8 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
-REFERENCES
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- 65 FR 77866: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
- 66 FR 21940: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2001.
- 67 FR 7164: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2002.
- 68 FR 42710: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2003.
- 69 FR 54144: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2004.
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