EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

progesterone
4-pregnen-3,20-dione

Supplier Sponsors

CAS Number: 57-83-0Picture of molecule3D/inchi
Other(deleted CASRN):257630-50-5
ECHA EINECS - REACH Pre-Reg:200-350-6
FDA UNII: 4G7DS2Q64Y
Nikkaji Web:J2.329I
Beilstein Number:1915950
MDL:MFCD00003658
XlogP3:3.90 (est)
Molecular Weight:314.46850000
Formula:C21 H30 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:white powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 121.00 °C. @ 760.00 mm Hg
Boiling Point: 447.15 °C. @ 760.00 mm Hg (est)
Vapor Pressure:3.590000 mmHg @ 25.00 °C. (est)
Flash Point: 332.00 °F. TCC ( 166.70 °C. ) (est)
logP (o/w): 3.870
Soluble in:
 water, 8.81 mg/L @ 25 °C (exp)
 water, 5.003 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Progesterone 98%
BOC Sciences
For experimental / research use only.
Progesterone ≥98%
Odor: characteristic
Use: Progesterone, synthesized from cholesterol by the sequential action of desmolase in the mitochondria, plays an important role in brain function as a endogenous progesterone receptor (PR) agonist (EC50 = 0.5 nM). Endogenous progesterone receptor (PR) agonist
Glentham Life Sciences
Progesterone
Indis NV
For experimental / research use only.
Progesterone
Maypro Industries
Progesterone
Meafo
For experimental / research use only.
Progesterone
Penta International
PROGESTERONE MICRONIZED POWDER USP
Penta International
PROGESTERONE WETTABLE POWDER USP
Sigma-Aldrich: Sigma
For experimental / research use only.
Progesterone ≥99%
WholeChem
Progesterone
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intravenous-mouse LDLo 100 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD LUNGS, THORAX, OR RESPIRATION: DYSPNEA BEHAVIORAL: ATAXIA
Journal of Medicinal Chemistry. Vol. 11, Pg. 117, 1968.

intraperitoneal-rat LD50 327 mg/kg
Drugs in Japan Vol. -, Pg. 1183, 1995.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
pharmaceuticals / chemical synthisis
Recommendation for progesterone usage levels up to:
 not for fragrance use.
 
Recommendation for progesterone flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov:search
Daily Med:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA GENetic TOXicology:Search
EPA Substance Registry Services (TSCA):57-83-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5994
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(8S,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
Chemidplus:0000057830
EPA/NOAA CAMEO:hazardous materials
RTECS:TW0175000 for cas# 57-83-0
 
References:
 (8S,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5994
Pubchem (sid):134971194
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
Metabolomics Database:Search
KEGG (GenomeNet):C00410
HMDB (The Human Metabolome Database):HMDB01830
FooDB:FDB001871
Export Tariff Code:2937.92.8020
MedlinePlusSupp:View
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
•progesterone is available in an oily solution for injection, as pessaries or suppositories and as an intrauterine device. •prochieve is available in two strengths: 4% gel (45 mg of progesterone) and 8% gel (90 mg of progesterone). •progesterone injection, (projestaject, others) contains 25 to 100 mg progesterone per ml of vegetable oil. aqueous suspensions of progesterone are particularly painful & are seldom used. progesterone is also available in a t-shaped intrauterine contraceptive device that provides continuous delivery of progesterone in the uterine cavity for 1 yr. this is marketed under the name of progestasert and contains 38 mg of progesterone. •vials (aqueous solution and in oil), 25 mgml, 50 mgml, and 100 mgml. intrauterine system, 38 mg, provides contraceptive effectiveness for a period of one year. •grade: national formulary •progesterone exists in two crystalline forms (alpha- and beta-) of equal physiological activity. •alza corp...developed and intrauterine device, progestasert, designed to release progesterone by diffusion through a rate-controlling membrane for up to one year.
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 apple
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 bean mung bean
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 not found in nature
 onion
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 pea
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 phaseolus angularis
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 potato
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 rice
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 tomato
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Synonyms:
(8S,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
 agolutin
 akrolutin
 bio-luton
 colprosterone
 corlutin
 corluvite
 corporin
 crinone
 cyclogest
 duraprogen
 endometrin
 estima
 flavolutan
 fologenon
 gesterol 100
 gesterol 50
 gestiron
 gestone
 gestormone
 gestron
 glanducorpin
 gynlutin
 gynoluton
 hormoflaveine
 hormoluton
 lingusorbs
 lipolutin
 lucorteum
 lugesteron
 luteodyn
 luteol
 luteosan
 luteostab
 luteovis
 luteum
 lutociclina
 lutocuclin M
 lutocyclin
 nalutron
 percutacrine
 piaponon
 pregn-4-en-3,20-dione
(S)-pregn-4-en-3,20-dione
 pregn-4-ene-3,20-dione
4-pregnen-3,20-dione
(S)-4-pregnene-3,20-dione
 progeffik
 progestan
 progestasert
(S)-progesterone
 progestogel
 progestol
 prontogest
 syngesterone
 synovex S
 utrogest
 vitarrine
 

Articles:

PubMed:Effects of ractopamine hydrochloride and zilpaterol hydrochloride supplementation on longissimus muscle shear force and sensory attributes of calf-fed Holstein steers.
PubMed:Transcript profiling of candidate genes in testis of pigs exhibiting large differences in androstenone levels.
PubMed:Effects of growth implants on consumer perceptions of meat tenderness in beef steers.
PubMed:Persistence of flavor neophobia as an indicator of state-dependent retention induced by pentobarbital, stress, and estrus.
 
Notes:
the major progestational steroid that is secreted primarily by the corpus luteum and the placenta. progesterone acts on the uterus, the mammary glands and the brain. it is required in embryo implantation; pregnancy maintenance, and the development of mammary tissue for milk production. progesterone, converted from pregnenolone, also serves as an intermediate in the biosynthesis of gonadal steroid hormones and adrenal corticosteroids. Progestational hormone secreted by corpus luteum during menstrual cycle. Also found in the gonads and haemolymph of crustaceans, e.g. Artemia, Euphosia, Homarus, Pandalus and Penaeus spp (CCD)
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