ESTRADIOL |
PRODUCT
IDENTIFICATION
|
CAS
NO. |
50-28-2;
873662-39-6 (beta) 57-91-0 (alpha) |
|
EINECS
NO. |
200-023-8 |
FORMULA |
C18H24O2 |
MOL
WT. |
272.39 |
H.S.
CODE
|
2937.92.0000
|
TOXICITY
|
Rat LD (Subcutaneous):> 300mg/kg |
SYNONYMS |
3,17-beta-Dihydroxyoestra-1,3,5-triene;
17-beta-OH-estradiol; |
1,3,5-Estratriene-3,17-beta-diol;
17-beta-Estra-1,3,5(10)-triene-3,17-diol; 17-beta-OH-oestradiol;
17-beta-Oestra-1,3,5(10)-triene-3,17-diol; Oestradiol;
17beta-Oestra-1,3,5(10)-triene-3,17-diol; 3,17-Epidihydroxyestratriene;
3,17-beta-Dihydroxy-1,3,5(10)-oestratriene; Estradiolum;
3,17-beta-Dihydroxyestra-1,3,5(10)-triene; 3,17-beta-Estradiol;
Estradiol-17beta; 3,17-beta-Oestradiol; 3,17beta-Dihydroxyestra-1,3,5-triene;
Dihydrofolliculin; Dihydrotheelin; Dihydroxyestrin;
3,17beta-Dihydroxyoestra-1,3,5-triene;
Estra-1,3,5(10)-triene-3,17-beta-diol; Oestra-1,3,5(10)-triene-3,17-beta-diol;
cis-estradiol; 3,17-epidihydroxyestratriene; Dihydrofollicular hormone;
Estrovite; Femestral; Femogen; Gynergon; Gynestrel; Ovahormon; Ovocycline;
Primofol; Progynon; Dimenformon; Dimenformon Prolongatum;
Diogyn; 3,17-beta-Dihydroxy-1,3,5(10)-estratriene; |
SMILES |
C1[C@H]2[C@H]3[C@@H](c4c(cc(O)cc4)CC3)CC[C@@]2([C@H](O)
C1)C
|
CLASSIFICATION
|
Steroid,
Steroid Hormone, Estrogen, Estrogen Modulator, Biochemicals
ex Plants, Hormone Antagonist.
|
PHYSICAL
AND CHEMICAL PROPERTIES
|
PHYSICAL
STATE |
white
to off-white crystalline powder |
MELTING
POINT |
173 - 179 C |
BOILING
POINT |
|
SPECIFIC
GRAVITY |
|
SOLUBILITY
IN WATER |
practically insoluble
(3.6 mg/l)
|
SOLVENT
SOLUBILITY
|
soluble
in alcohol, acetone and dioxane, sparingly soluble in
vegetable oils
|
pH |
|
log Pow |
4.01
(Octanol-water) |
VAPOR
PRESSURE |
1.26E-08 (mmHg at 25 C) |
HENRY'S LAW |
3.64E-11 (atm-m3/mole at 25 C) |
OH RATE |
1.23E-10 (cm3/molecule-sec
at 25 C Atmospheric) |
AUTOIGNITION
|
|
NFPA
RATINGS
|
Health:
2 Flammability: 0 Reactivity: 0 |
REFRACTIVE
INDEX
|
|
FLASH
POINT |
|
STABILITY |
Stable
under ordinary conditions |
GENERAL
DESCRIPTION & EXTERNAL LINKS
|
Estrogen is a mammalian estrogenic hormone naturally produced by follicle cells
of the vertebrate ovary, placenta, testis, and adrenal cortex. It is involved in
implantation of the fertilized ovum, acceleration of maturation, and the
maintenance of secondary sex characters and female reproductive organs such as
mammary glands, uterus, vagina, and fallopian tubes. Estradiol is most potent
mammalian estrogenic hormone. It is produced semi-synthetically for estrogen
replacement therapy in the treatment of female hypogonadism, vasomotor symptoms,
abnormal uterine bleeding, and primary ovarian failure. It is also used as a
feed additive as a growth promoter. There are two isomers: estradiol-17beta (the
principally active one) and estradiol-17alpha (inactive). It provokes ICSH
(interstitial-cell-stimulating hormone) secretion and proliferation of the human
endometrium. Estrogen includes
Estrogen
|
CAS
RN
|
Diethylstilbestrol
diphosphate |
522-40-7 |
Equilin
|
474-86-2 |
Estradiol cypionate |
313-06-4 |
Estradiol enanthate |
4956-37-0 |
Estradiol undecylate |
3571-53-7 |
Estradiol valerate |
979-32-8 |
Estradiol |
50-28-2 |
Estratab |
12126-59-9 |
Estriol |
50-27-1 |
Estrofurate |
10322-73-3 |
Estrone Sodium Sulfate |
438-67-5 |
Estrone |
53-16-7 |
Estropipate |
7280-37-7 |
Ethinyl estradiol
|
57-63-6 |
Fenestrel |
7698-97-7 |
Mestranol |
72-33-3 |
Nylestriol |
39791-20-3 |
Quinestrol |
152-43-2 |
Wikipedia
Linking: http://en.wikipedia.org/wiki/Estradiol
http://biomarkers.uchicago.edu/ Estradiol
(Salivary Estradiol Measurement in Wave I of the Social
Life Health & Aging Project)
http://itech.dickinson.edu/
- Estradiol is a sex hormone present in both females and males.
- Estradiol is one of the three naturally occuring estrogens in females, along
with estriol and estrone
- It is present in women from puberty until menopause
- It is essential for the reproductive system, as well as for sexual
reasons
- Affects many of the body’s major systems
- Synthetic estradiol is used in the pill, for hormone replacement therapy in
transsexuals, and for postmenopausal women
- Estradiol is derived from cholesterol which is converted into
androstenedione. Androstendione is then converted to testosterone which in turn
is converted to estradiol
|
SALES
SPECIFICATION |
APPEARANCE
|
white
to off-white crystalline powder |
IDENTIFICATION
|
Pass
Test A(IR), B(UV)
|
ASSAY
|
97.0
- 103.0%
|
OPTICAL
ROTATION
|
+76° ~ +83° |
MELTING
POINT
|
173
- 179 C
|
WATER
|
3.5%
max
|
IMPURITY
|
Individual
impurity 0.2%
max, Total impurity 0.5% max
|
TRANSPORTATION |
PACKING |
|
HAZARD
CLASS |
|
UN
NO. |
|
OTHER
INFORMATION |
Hazard Symbols: T, Risk Phrases: 45-63,
Safety
Phrases: 53-26-36/37/39 |
|
|