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gemeprost

CAS No.
64318-79-2
Chemical Name:
gemeprost
Synonyms
D02073;Cergem;ONO 802;Carprost;Cervagem;SC 37681;Cervageme;gemeprost;Preglandin;Preglandin (tn)
CBNumber:
CB0875558
Molecular Formula:
C23H38O5
Molecular Weight:
394.548
MDL Number:
MFCD00867892
MOL File:
64318-79-2.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:41

gemeprost Properties

Boiling point 438.73°C (rough estimate)
Density 1.0380 (rough estimate)
refractive index 1.5800 (estimate)
pka 13.84±0.60(Predicted)
FDA UNII 45KZB1FOLS
ATC code G02AD03

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS06
Signal word  Danger
Hazard statements  H332-H360-H301-H312
Precautionary statements  P261-P271-P304+P340-P312-P264-P270-P301+P310-P321-P330-P405-P501-P280-P302+P352-P312-P322-P363-P501
RIDADR  3249
HazardClass  6.1(b)
PackingGroup  III

gemeprost price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC G305040 Gemeprost 64318-79-2 5mg $2810 2021-12-16 Buy
American Custom Chemicals Corporation API0002815 GEMEPROST 95.00% 64318-79-2 500ML $4138.37 2021-12-16 Buy
American Custom Chemicals Corporation API0002815 GEMEPROST 95.00% 64318-79-2 5ML $787.71 2021-12-16 Buy
Medical Isotopes, Inc. 18648 Gemeprost 64318-79-2 5mg $950 2021-12-16 Buy
American Custom Chemicals Corporation API0002815 GEMEPROST 95.00% 64318-79-2 100ML $2365.44 2021-12-16 Buy
Product number Packaging Price Buy
G305040 5mg $2810 Buy
API0002815 500ML $4138.37 Buy
API0002815 5ML $787.71 Buy
18648 5mg $950 Buy
API0002815 100ML $2365.44 Buy

gemeprost Chemical Properties,Uses,Production

Description

Gemeprost, a metabolically stabilized analog of PGE1, has been demonstrated to reliably induce termination of early pregnancy when administered as a vaginal suppository. Its effect is presumably due to both uterine contraction and rapid decline of steroid hormone levels. Minimal side effects have been reported.

Originator

Ono (Japan)

Uses

Prostaglandin.

Uses

Gemeprost is an analogue of Prostaglandin (P838600). Gemeprosts, similarly to Nitric Oxide donors, induce uterine cervical dilation and are used before surgical termination of pregnancy.

Definition

ChEBI: Gemeprost is an aliphatic alcohol.

Manufacturing Process

Synthesis of 9-oxo-1α,15α-bis-(2-tetrahydropyranyloxy)-16,16-dimethylprosta-trans-2, trans-13-dienoic acid: 4 g of ethyl 9α-hydroxy-11α15α-bis-(2- tetrahydropyranyloxy)-16,16-dimethyl-prosta-trans-2,trans-13-dienoate were dissolved in 130 ml of a mixture of ethanol-water (3:1), mixed with 3.9 g of potassium hydroxide and stirred at 25°C for 2 hours. The reaction mixture was acidified with aqueous solution of oxalic acid to pH 5, and diluted with 100 ml of water, extracted with ethyl acetate. The extracts were washed with water, dried over sodium sulfate and concentrated under reduced pressure to obtain 3.88 g of 9α-hydroxy-11α,15α-bis-(2-tetrahydropyranyloxy)-16,16- dimethyl-prosta-trans-2,trans-13dienoic acid.
The obtained compound 2.46 g were dissolved in 72 ml of diethyl ether and stirred at 3°C. To which a solution of manganese sulfate (15 g), 3.1 g of chromium trioxide, 72 ml of water and 3.5 ml of sulfuric acid was added. After stirring for 3.5 hours at 3°C, extracted with diethyl ether. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate-benzene (1:1) as eluent to give 2.35 g of the title compound.
Synthesis of 16,16-dimethyl-trans-δ2-PGE1: 2.35 g of the bistetrahydropyranyl ether were dissolved in 6 ml of tetrahydrofuran and 60 ml of 65%-acetic acid aqueous solution and the solution stirred at 60°C to 70°C for 20 minutes. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water, dried and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate-cyclohexane (2:3) as eluent to yield 270 mg of the title compound.

brand name

CERVAGEM

Therapeutic Function

Prostaglandin, Cervical softener

gemeprost Preparation Products And Raw materials

Global( 40)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9320 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418684 +8618949823763 sales@tnjchem.com China 25363 58
ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
+86-19164747840 +86-13119157289 13119157289@163.com China 2971 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58

View Lastest Price from gemeprost manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
gemeprost pictures 2019-07-10 gemeprost
64318-79-2
US $7.00 / KG 1KG 99% 1000KG Career Henan Chemical Co
  • gemeprost pictures
  • gemeprost
    64318-79-2
  • US $7.00 / KG
  • 99%
  • Career Henan Chemical Co
trans-2,3-Didehydro-16,16-dimethyl PGE1 methyl ester (2E,13E,15R)-11α,15-Dihydroxy-16,16-dimethyl-9-oxoprosta-2,13-dien-1-oic acid methyl ester (E)-7-[(1R,2R,3R)-3-Hydroxy-2-[(E,R)-3-hydroxy-4,4-dimethyl-1-octenyl]-5-oxocyclopentyl]-2-heptenoic acid methyl D02073 Gemeprost (jan/usan/inn) Preglandin (tn) 16,16-Dimethyl-trans-Δ2-PGE methyl ester 16,16-Dimethyl-trans-Δ2-PGE1 methyl ester 16,16-Dimethyl-trans-Δ2-prostaglandin E1 methyl ester Carprost Cergem Cervagem Cervageme Methyl 16,16-dimethyl-trans-Δ2-PGE1 gemeprost ONO 802 Preglandin SC 37681 gemeprostaglandin gemeprost USP/EP/BP 64318-79-2