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Desogestrel

CAS No.
54024-22-5
Chemical Name:
Desogestrel
Synonyms
Desogestrel for system suitability CRS;Desogen;Desogestrel CRS;org2969;Cyclosa;Dicromil;DESTODENE;Cerazette;DESOGESTREL;DESOGESTRAL
CBNumber:
CB2359630
Molecular Formula:
C22H30O
Molecular Weight:
310.47
MDL Number:
MFCD00869346
MOL File:
54024-22-5.mol
MSDS File:
SDS
Last updated:2024-03-13 16:52:01

Desogestrel Properties

Melting point 109-110°C
alpha D20 +55° (chloroform)
Boiling point 390.62°C (rough estimate)
Density 1.0169 (rough estimate)
refractive index 1.5100 (estimate)
storage temp. -20°C Freezer
solubility Practically insoluble in water, very soluble in methanol, freely soluble in anhydrous ethanol and in methylene chloride.
pka 13.07±0.40(Predicted)
color White to Almost white
Merck 14,2926
FDA UNII 81K9V7M3A3
NCI Drug Dictionary Cerazette
ATC code G03AC09

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS09
Signal word  Danger
Hazard statements  H360FD-H410
Precautionary statements  P202-P273-P280-P308+P313-P391-P405
Safety Statements  24/25
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
RTECS  JF7975000
HS Code  29372390

Desogestrel price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 1173235 Desogestrel United States Pharmacopeia (USP) Reference Standard 54024-22-5 100mg $436 2024-03-01 Buy
Sigma-Aldrich 32809 Desogestrel VETRANAL 54024-22-5 25mg $164 2022-05-15 Buy
Sigma-Aldrich 1173235 Desogestrel United States Pharmacopeia (USP) Reference Standard 54024-22-5 50mg $452 2022-05-15 Buy
TCI Chemical D4163 Desogestrel >98.0%(HPLC) 54024-22-5 100mg $159 2024-03-01 Buy
Cayman Chemical 23651 Desogestrel ≥95% 54024-22-5 5mg $61 2024-03-01 Buy
Product number Packaging Price Buy
1173235 100mg $436 Buy
32809 25mg $164 Buy
1173235 50mg $452 Buy
D4163 100mg $159 Buy
23651 5mg $61 Buy

Desogestrel Chemical Properties,Uses,Production

Description

Desogestrel is a synthetic progestogen. It inhibits ovulation and prevents fertilization in rabbits and mice. Desogestrel inhibits rhodamine 123 efflux, a measure of P-glycoprotein activity, ex vivo in human lymphocytes and CD8+ T cells in a dose-dependent manner. Formulations containing desogestrel have been used as oral contraceptives and for the treatment of polycystic ovary syndrome.

Chemical Properties

White Solid

Originator

Dicromil,Organol ,W. Germany,1981

Uses

A progestogen with low androgenic potency

Definition

ChEBI: Desogestrel is a 17beta-hydroxy steroid and a terminal acetylenic compound. It has a role as a contraceptive drug, a progestin and a synthetic oral contraceptive.

Manufacturing Process

A solution of 1.0 g of 11,11-methylene-18-methyl-delta4-estren-17-one in 33 ml tetrahydrofuran was added to a potassium-acetylide solution in tetrahydrofuran.
After 2 hours of stirring at 0°C to 5°C the reaction mixture was acidified with 2N H2SO4and processed further.
By a chromatographic treatment on silica gel and crystallization from pentane 0.7 g of 11,11-methylene-17α-ethynyl-18-methyl-δ4-estren-17β-ol with a melting point of 109°C to 110°C and an [α]D of +55°C (CHCl3) was obtained.

Therapeutic Function

Progestin

General Description

Desogestrel, (17α)-13-ethyl-11-methylene-18,19-dinorpregn-4-en-20-yn-17-ol, is a 19-nortestosterone analog with good progestin activity. Likethe other progestins, it is orally active and used in combinationwith an estrogen in oral contraceptives. Desogestrel is aprodrug that must be oxidized to the 3-one in vivo to haveprogestational action. CYPs 2C9 and 2C19 have been implicatedin the initial hydroxylation of desogestrel at C3.

Clinical Use

Desogestrel also is a prodrug and is rapidly metabolized in the intestinal mucosa and on first pass through the liver to its active metabolite, etonogestrel (3-ketodesogestrel). Following oral administration, the relative bioavailability for desogestrel is approximately 84%. Desogestrel also exhibits high selectivity for the progesterone receptor and low and rogenic activity, and it does not diminish the beneficial effects of estrogen on the lipid profile.

54024-21-4
1066-54-2
54024-22-5
Synthesis of Desogestrel from 13b-Ethyl-11-methylenegon-4-en-17-one and Trimethylsilylacetylene

Desogestrel Preparation Products And Raw materials

Global( 318)Suppliers
Supplier Tel Email Country ProdList Advantage
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 616 58
Henan Tianfu Chemical Co.,Ltd.
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Hebei shuoxi biotechnology co. LTD
+8613081092107 CHINA 968 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-519-519-85557386 marketing1@neostarunited.com China 8349 58

View Lastest Price from Desogestrel manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Desogestrel pictures 2024-04-22 Desogestrel
54024-22-5
US $0.00-0.00 / kg 1kg 98% 20tons Sinoway Industrial co., ltd.
Desogestrel pictures 2024-04-17 Desogestrel
54024-22-5
US $1.10 / g 1g 99.0% min 100 tons min Shaanxi Dideu Medichem Co. Ltd
Desogestrel pictures 2024-03-08 Desogestrel
54024-22-5
US $10.00 / kg 1kg 99% 1000kg Nantong Guangyuan Chemicl Co,Ltd
  • Desogestrel pictures
  • Desogestrel
    54024-22-5
  • US $0.00-0.00 / kg
  • 98%
  • Sinoway Industrial co., ltd.
  • Desogestrel pictures
  • Desogestrel
    54024-22-5
  • US $1.10 / g
  • 99.0% min
  • Shaanxi Dideu Medichem Co. Ltd
  • Desogestrel pictures
  • Desogestrel
    54024-22-5
  • US $10.00 / kg
  • 99%
  • Nantong Guangyuan Chemicl Co,Ltd

Desogestrel Spectrum

(17α)-13-Ethyl-11-methylene-18,19-dinorpregn-4-en-20-yn-17-ol (8S,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-11-methylidene-1,2,3,6,7,8,9,10,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ol (17R)-13-Ethyl-11-methylene-18,19-dinorpregn-4-en-20-yn-17-ol (8S,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-11-methylene-1,2,3,6,7,8,9,10,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ol Desogestrel (50 mg) DESTODENE Desogestrel for system suitability, European Pharmacopoeia (EP) Reference Standard Desogestrel, >=99% (8S,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-11-Methylene-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-ol 13-ethyl-11-methylene-19-dinorpregn-4-en-20-yn-17-o(17-alpha)-1 org2969 13-ethyl-11-methylene-18,19-dinor-17alpha-pregn-4-en-20-yn-17-ol DESOGESTREL (17a)-13-Ethyl-11-methylene-18,19-dinorpregn-4-en-20-yn-17-ol Cerazette Cyclosa Dicromil Marvelon 150/320 18,19-Dinorpregn-4-en-20-yn-17-ol, 13-ethyl-11-methylene-, (17.alpha.)- (17β)-13-Ethyl-11-methylene-19-nor-pregn-4-en-20-yn-17-ol DESOGESTRAL 13-Ethyl-11-methylene-18,19-dinor-17α-4-pregnen-20-yn-17-ol 13-ethyl-17-ethynyl-11-methylene-1,2,3,6,7,8,9,10,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ol Desogestrel, 99%, a third-generation 19-nortestosterone derivative progestogen Desogestrel Solution Desogestrel> Desogestrelum 18,19-Dinorpregn-4-en-20-yn-17-ol, 13-ethyl-11-methylene-, (17α)- Desogestrel USP/EP/BP DesogestrelQ: What is Desogestrel Q: What is the CAS Number of Desogestrel Q: What is the storage condition of Desogestrel Q: What are the applications of Desogestrel Desogestrel (1173235) Desogestrel for system suitability CRS Desogestrel CRS Desogen Desogestrol 54024-22-5 C22H30O Hormone Drugs Steroid and Hormone Intermediates & Fine Chemicals Pharmaceuticals Steroids API