desoxycorticosterone acetate, 56-47-3

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CODE123466 CODE123466
Product(s):
56-47-3 Deoxycorticosterone acetate >98%
Deoxycorticosterone acetate is a steroid hormone used for intramuscular injection for replacement therapy of the adrenocortical steroid.

CAS Number:	56-47-3	3D/inchi
Other(deleted CASRN):	106111-90-4
ECHA EINECS - REACH Pre-Reg:	200-275-9
FDA UNII:	6E0A168OB8
Nikkaji Web:	J4.569A
Beilstein Number:	2570798
MDL:	MFCD00003660
XlogP3:	3.10 (est)
Molecular Weight:	372.50484000
Formula:	C23 H32 O4
BioActivity Summary:	listing
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:information only not used for fragrances or flavors

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:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Melting Point:	157.00 °C. @ 760.00 mm Hg
Boiling Point:	504.10 °C. @ 760.00 mm Hg (est)
Flash Point:	424.00 °F. TCC ( 218.00 °C. ) (est)
logP (o/w):	3.080
Soluble in:
	water, 8.73 mg/L @ 25 °C (exp)
	water, 10.59 mg/L @ 25 °C (est)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

Suppliers:

BOC Sciences

For experimental / research use only.

Deoxycorticosterone acetate >98%

Odor: characteristic

Use: Deoxycorticosterone acetate is a steroid hormone used for intramuscular injection for replacement therapy of the adrenocortical steroid.

Matrix Scientific

For experimental / research use only.

3,20-Dioxopregn-4-en-21-yl acetate

sds

Santa Cruz Biotechnology

For experimental / research use only.

Desoxycorticosterone Acetate ≥97%

Sigma-Aldrich: Sigma

For experimental / research use only.

Desoxycorticosterone Acetate

sds

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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
information only not used for fragrances or flavors
Recommendation for desoxycorticosterone acetate usage levels up to:
	not for fragrance use.

Recommendation for desoxycorticosterone acetate flavor usage levels up to:
	not for flavor use.

Safety References:

EPI System: View

Chemical Carcinogenesis Research Information System:Search

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :5952

National Institute of Allergy and Infectious Diseases:Data

WGK Germany:3

[2-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

Chemidplus:0000056473

RTECS:HG0525000 for cas# 56-47-3

References:

	[2-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	5952
Pubchem (sid):	134972761

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
KEGG (GenomeNet):	C14554
HMDB (The Human Metabolome Database):	Search
Export Tariff Code:	2937.29.0050
ChemSpider:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

not found in nature

Synonyms:

21-	acetoxy-3,20-diketopregn-4-ene
21-	acetoxypregn-4-ene-3,20-dione
	arcort
	bio-corten
	cortacet
	cortate
	cortenil
	cortesan
	cortexone acetate
	corticosterone, deoxy-, acetate
	cortifar
	cortigen
	cortinaq
	cortiron
	cortivis
	cortixyl
	cortormon
	decorten
	decortin
	decorton
	decosteron
	decosterone
	decostrate
	deoxycorticosterone 21-acetate
11-	deoxycorticosterone 21-acetate
11-	deoxycorticosterone acetate
	deoxycortone acetate
	descornaq
	desocort
11-	desoxycorticosterone acetate
	desoxycorticosterone acetate [USP]
	desoxycorticosterone-21-acetate
	desoxycortone acetate
[2-[(8S,9S,10R,13S,14S,17S)-10,13-	dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate
	DOC acetate
	DOCA acetate
	DOXO
	doxycamon
21-	hydroxypregn-4-ene-3,20-dione 21-acetate
	krinocorts
	mincortid
	ocriten
	ocritena
	organon's DOCA acetate
	percorten
	percortene
	percotol
	pregn-4-ene-3,20-dione, 21-hydroxy-, acetate
4-	pregnene-3,20-dione 21-acetate
4-	pregnene-3,20-dione-21-ol acetate
	primocort
	primocortan
	sincortex
	steraq
	syncorta
	syncortyl
	unidocan

Articles:

PubMed:Salt appetite induced by DOCA treatment or adrenalectomy in rats: analysis of ingestive behavior.

PubMed:Angiotensin and salt appetite: physiological amounts of angiotensin given peripherally increase salt appetite in the rat.

PubMed:Accumulation of glycoprotein gonadotropin in the pituitary of juvenile rainbow trout in response to androgens and C21-steroids, including 11-steroids.

Notes:

the 21-acetate derivative of desoxycorticosterone.

desoxycorticosterone acetate 4-pregnene-3,20-dione-21-ol acetate

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Articles:

desoxycorticosterone acetate
4-pregnene-3,20-dione-21-ol acetate