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Estriol API content appearance, production process, usage and dosage, chemical properties, product data

Estriol API content appearance, production process, usage and dosage, chemical properties, product data

Estriol API content appearance, production process, usage and dosage, chemical properties, product data
Estriol API content appearance, production process, usage and dosage, chemical properties, product data Estriol API content appearance, production process, usage and dosage, chemical properties, product data Estriol API content appearance, production process, usage and dosage, chemical properties, product data

Large Image :  Estriol API content appearance, production process, usage and dosage, chemical properties, product data Get Best Price

Product Details:

Place of Origin: CHINA
Brand Name: DKY
Certification: GMP,ISO9001
Model Number: USP,CP

Payment & Shipping Terms:

Minimum Order Quantity: kg
Price: USD3600/KG
Packaging Details: 1 kg aluminum tin barrel
Delivery Time: 1days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 500KG
Detailed Product Description
Use: Estrogen And Progesterone Purity: 99%
Cas No.: 50-27-1 Appearance: White Powder
Shelf Life: 2 Years Einecs No.: 200-022-2
High Light:

female estrogen raw material

,

female hormones estrogen

Product Name: Estriol
Synonyms: TRIDESTRIN;16-alpha,17-beta-oestriol;16alpha,17beta-Oestriol;16alpha-Estriol;16-alpha-hydroxyoestradiol;16alpha-Hydroxyoestradiol;3,16-alpha,17-beta-estriol;3,16alpha,17beta-Estriol
CAS: 50-27-1
MF: C18H24O3
MW: 288.38
EINECS: 200-022-2

 

 

Estriol Chemical 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)
Fp 9℃
storage temp. -20°C Freezer

 

Chemical Properties White or almost white, crystalline powder.
Uses 17b-estradiol metabolite, primary estrogen in urine
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).

 

 

Uses It belongs to estrogen drug. It can be used for treating leukopenia, various kinds of menopathy, senile vaginitis, and menopausal syndrome. You may also get temporary breast swelling and lumps, menstrual cycle disorders with self-recovery after stopping the drug for about 1 month. Patients of breast hyperplasia, breast lumps, and cancer potentially being related to female hormone-related cancer, aplastic anemia and liver disease patients should be disabled.
Production method Take estrone as raw material; go through acetylation, epoxidation, and reduction to obtain the estriol products.
Estrone [acetylation] → [16, 17-epoxidation] → [rearrangement] → [Restore] → [hydrolysis] → finished product of estriol.
Estrone acetate successively goes through followed enolization, acetylation, epoxidation and reduction to obtain it.

Estriol API content appearance, production process, usage and dosage, chemical properties, product data 0

 

Natural hormone Estriol belongs to natural hormone and is the metabolite of estradiol in vivo. It is mainly presented in the urine. Estrogen has a relative small activity with the oral activity being 6 times as high as estrone but being weaker than estradiol with non-carcinogenic effects. After its administration, the in vivo estradiol levels did not change. Estriol has selective action on the vaginal and cervical canal but has no effect on the uterus and endometrium entity. Animal experiments have shown that estriol has a stronger effect on vaginal epithelial keratosis than estradiol, thus being able to promote vaginal epithelial hyperplasia, superficial cells keratosis, mucosal angiogenesis and vaginal epithelial wound healing, but having a weak effect on the weight gain of mouse uterus. At the same time, estriol can enhance the function of cervix cell, causing the cervix muscle fiber hyperplasia and increasing the cervical elasticity and softness. In addition, estriol has feedback inhibition on the hypothalamus and pituitary but does not inhibit ovulation while only having significant impact on the corpus luteum and therefore can be used as the auxiliary drug in the medium-term labor induction and artificial abortion and for the treatment of various kinds of menopathy. Estriol also has significant effect on the hematopoietic system and can reduce vascular permeability and fragility. Therefore, it can be used for the treatment of various kinds of hemorrhage. It also has effect of rapidly increasing the peripheral leukocytes and generally begins to take effect at 1 to 3 days after treatment but with a shorter duration of action and is effective in treatment the leukopenia induced by radiotherapy and chemotherapy.

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