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Estrone Chemical Sampling Information
Estrone

General Description
    Synonyms: Aquacrine; Crinovaryl; 1,3,5-Estratriene-3-ol-17-one; Erystogen; 3-Hydroxyestra-1,3,5(10)-trien-17-one; Menagen

    OSHA IMIS Code Number: E320

    Chemical Abstracts Service (CAS) Registry Number: 53-16-7

    NIOSH, Registry of Toxic Effects (RTECS) Identification Number: KG8575000

    Chemical Description and Physical Properties: Solid white powder.
      molecular formula: C18H22O2
      molecular weight: 270.37
      melting point: 254-256°C
    Potentially hazardous incompatibilities:
Health Factors
    National Toxicology Program (NTP) carcinogenic classification: Known to be a Human Carcinogen (estrogens, steroidal)

    Potential symptoms: IN MEN: Possible anorexia, nausea, vomiting, edema; feminization (gynecomastia, erectile dysfunction, atrophy of secondary sex organs, oligospermia); IN WOMEN: Breast tension or pain; cervical hypersecretion; menstrual disorders (menorrhagia, metrorrhagia); nausea, headache; fluid retention, hypertension, leg cramps, vision disturbances; endometriosis pain; possible decrease in milk production by lactating mothers.

    Health Effects: Known human (female) carcinogen (HE2).

    Affected organs: Male and female reproductive systems

    Notes:
    1. Estrone is an OSHA Select carcinogen.
    2. Estrone is synthesized from androstenedione via aromatase (CYP19) and from estradiol by 17-hydroxysteroid dehydrogenase.
    3. Affinities of estrone for the two estrogen receptors, α and ß, are approximately 1/2 and 1/3, respectively, of the affinities of these receptors for estradiol-17ß.
    4. Mean serum estrone levels in samples from postmenopausal women of unknown ovarian status were reported to be about half the levels of estrone found in samples from men in the same age range.

    Date Last Revised: 03/10/2006

    Literature Basis:
    • No Author: Estrogens, Steroidal. Report on Carcinogens, Eleventh Edition; U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program, 2005.
    • de Ronde, W., Hofman, A., Pols, H.A.P. and de Jong, F.H.: A direct approach to the estimation of the origin of oestrogens and androgens in elderly men by comparison with hormone levels in postmenopausal women. Eur. J. Endocrinol. 152(2): 261-268, 2005.
    • Kuiper, G.G.J.M., et al.: Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors α and ß. Endocrinology 138(3): 863-870, 1997.
    • Loose-Mitchell, D.S. and Stancel, G.M.: Estrogens and Progestins (Chapter 58). In, Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 10th Ed. J.G. Hardman, L.E. Limbird and A.G. Gilman, eds. New York: McGraw-Hill, 2001, pp. 1597-1634.
    • Pohanish, R.P. (editor): Estrone. In, Sittig’s Handbook of Toxic and Hazardous Chemicals and Carcinogens, Fourth Ed., Vol. 1. Norwich, NY: Noyes Publications, William Andrew Publishing, 2002, pp. 1025-1027.
    • Zeleniuch-Jacquotte, A., et al.: Postmenopausal endogenous oestrogens and risk of endometrial cancer: results of a prospective study. Br. J. Cancer 84(7): 975-981, 2001.
Monitoring Methods used by OSHA
    Laboratory Sampling/Analytical Method:

    • sampling media: Glass Fiber Filter (37 mm) in 3-piece cassette
      analytical solvent: Methanol
      maximum volume: 240 Liters   maximum flow rate: 1.0 L/min   maximum time: 240 Minutes
      current analytical method: High Performance Liquid Chromatography; HPLC/UV at 280nm
      method reference: OSHA Analytical Method (OSHA PV2001)
      method classification: Partially Validated
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  Chemical Sampling Information:
  Estrone
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Page last updated: 03/30/2007
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