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Estriol

Estriol Structure
CAS No.
50-27-1
Chemical Name:
Estriol
Synonyms
E 3;OVESTIN;16α-Estriol;ESTRA-1,3,5(10)-TRIENE-3,16,17-TRIOL;(16alpha,17beta)-Estra-1,3,5(10)-triene-3,16,17-triol;1,3,5(10)-Estratriene-3,16α,17β-triol, 16α-Hydroxyestradiol, 3,16α,17β-Trihydroxy-1,3,5(10)-estratriene;Estriol,1,3,5(10)-Estratriene-3,16α,17β-triol, 16α-Hydroxyestradiol, 3,16α,17β-Trihydroxy-1,3,5(10)-estratriene;(8R,9S,13S,14S,16R,17R)-13-Methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,16,17-triol;OE3;Holin
CBNumber:
CB1687589
Molecular Formula:
C18H24O3
Molecular Weight:
288.38
MOL File:
50-27-1.mol
Modify Date:
2024/5/6 18:26:58

Estriol Properties

Melting point 280-282 °C(lit.)
alpha D25 +58° ±5° (0.04 g in 1 ml dioxane)
Boiling point 370.61°C (rough estimate)
Density 1.27
refractive index 58 ° (C=0.4, Dioxane)
Flash point 9℃
storage temp. 2-8°C
solubility Practically insoluble in water, sparingly soluble in ethanol (96 per cent).
pka pKa 10.38±0.02(H2O t=23±2 Iunspeci?ed) (Uncertain)
color White to Off-White
Water Solubility 3.2mg/L(25 ºC)
Merck 3707
BRN 2508172
InChIKey PROQIPRRNZUXQM-ZXXIGWHRSA-N
CAS DataBase Reference 50-27-1(CAS DataBase Reference)
NIST Chemistry Reference Estriol(50-27-1)
EPA Substance Registry System Estriol (50-27-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H351-H360FD-H362
Precautionary statements  P201-P202-P260-P263-P264-P308+P313
Hazard Codes  T,F
Risk Statements  60-61-40-45-39/23/24/25-23/24/25-11
Safety Statements  53-22-36/37/39-45-36/37-16
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  3
RTECS  KG8225000
8-10
HS Code  29072990
Toxicity LD50 oral in rat: > 2gm/kg
NFPA 704
3
0 0

Estriol price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) E1253 Estriol ≥97% 50-27-1 100MG ₹6462.53 2022-06-14 Buy
Sigma-Aldrich(India) E1253 Estriol ≥97% 50-27-1 500MG ₹7902.25 2022-06-14 Buy
Sigma-Aldrich(India) PHR2800 Estriol certified reference material, pharmaceutical secondary standard 50-27-1 200MG ₹22342.8 2022-06-14 Buy
Sigma-Aldrich(India) E1253 Estriol ≥97% 50-27-1 1G ₹12199.78 2022-06-14 Buy
Sigma-Aldrich(India) E1149 Estriol meets USP testing specifications 50-27-1 1G ₹11387.9 2022-06-14 Buy
Product number Packaging Price Buy
E1253 100MG ₹6462.53 Buy
E1253 500MG ₹7902.25 Buy
PHR2800 200MG ₹22342.8 Buy
E1253 1G ₹12199.78 Buy
E1149 1G ₹11387.9 Buy

Estriol Chemical Properties,Uses,Production

Description

Estriol is significantly less active than estradiol; however, it has a selective ability to stimulate blood flow and restoration of genital epithelium. In addition, using this drug reduces mental symptoms of menopausal syndrome. It is used in the premenopausal and menopausal periods, for skin atrophy and signs of genital degeneration, and so on.

Chemical Properties

White or almost white, crystalline powder.

Uses

A metabolite of Estradiol. An estrogenic metabolite considerably less potent than the hormone Estradiol

Definition

ChEBI: A 3-hydroxy steroid that is estra-1,3,5(10)-trien-3-ol substituted by additional hydroxy groups at positions 16 and 17 (16alpha,17beta-stereoisomer).

General Description

Estriol, estra-1,3,5(10)-triene-3,16 ,17 -triol, is available for compounding into several differentformulations for use in HRT. It can be used alone or in combinationswith estradiol (Bi-Est) or with estradiol and estrone(Tri-Est).

Hazard

A carcinogen (OSHA).

Safety Profile

Suspected carcinogen with experimental carcinogenic, neoplastigenic, tumorigenic, and teratogenic data. Other experimental reproductive effects. Mutation data reported. A steroid drug for the treatment of menopause. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Crystallise estriol from EtOH/ethyl acetate. Also purify it by countercurrent distribution with cyclohexane/EtOAc (1:1) and EtOH/H2O (1:1). The UV (EtOH) has max at 280nm ( 2,090 M-1cm-1). [Huffmann & Lott 71 719 1949, Leeds et al. J Am Chem Soc 76 2943 1954, Beilstein 6 IV 7550.]

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