A3951212
Estriol , Analysis standard , 50-27-1
Synonym(s):
1,3,5(10)-Estratriene-3,16α,17β-triol;16α-Hydroxyestradiol;3,16α,17β-Trihydroxy-1,3,5(10)-estratriene;Estriol
CAS NO.:50-27-1
Empirical Formula: C18H24O3
Molecular Weight: 288.38
MDL number: MFCD00003691
EINECS: 200-022-2
Pack Size | Price | Stock | Quantity |
100MG | RMB622.40 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT 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) |
form | Solid |
color | White to Off-White |
optical activity | +6127 (95% ethanol) |
Water Solubility | 3.2mg/L(25 ºC) |
Merck | 3707 |
BRN | 2508172 |
InChIKey | PROQIPRRNZUXQM-ZXXIGWHRSA-N |
Description and Uses
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.
A metabolite of Estradiol (E888000). An estrogenic metabolite considerably less potent than the hormone Estradiol (E888000).
Safety
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 |
F | 8-10 |
HS Code | 29072990 |
Toxicity | LD50 oral in rat: > 2gm/kg |