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adenosine phosphate
adenosine 5'-phosphate

Sponsors

Name:[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyldihydrogen phosphate
CAS Number: 61-19-8Picture of molecule3D/inchi
Other:162756-82-3
ECHA EINECS - REACH Pre-Reg:200-500-0
FDA UNII:415SHH325A
Nikkaji Web:J4.814C
MDL:MFCD00149360
XlogP3:-3.50 (est)
Molecular Weight:347.22474200
Formula:C10 H14 N5 O7 P
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Category:cosmetic ingredient for skin conditioning
 
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
 FDA/DG SANTE Petitions, Reviews, Notices:
GRN 144 Adenosine 5'-monophosphoric acid and its monosodium and disodium salts View-notice PDF
 
Physical Properties:
Appearance:white crystalline powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 195.00 °C. @ 760.00 mm Hg
Soluble in:
 water, 8510 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
 
Suppliers:
BOC Sciences
For experimental / research use only.
Adenosine monophosphate > 95%
Odor: characteristic
Use: Adenosine monophosphate is a natural occurring nucleotide and a useful ligand determinant that facilitate the binding of APS reductase inhibitors and activates adenosine receptor agonists.
Changzhou Longo Chemical
Adenosine 5'-monophosphate
George Uhe Company
Adenosine Phosphate
Penta International
ADENOSINE 5'-MONOPHOSPHATE
Sigma-Aldrich: Sigma
For experimental / research use only.
Adenosine 5'-monophosphate monohydrate from yeast, ≥97%
 
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:
intraperitoneal-mouse LD50 4000 mg/kg
Pharmaceutical Chemistry Journal Vol. 20, Pg. 160, 1986.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: cosmetic ingredient for skin conditioning
Recommendation for adenosine phosphate usage levels up to:
 not for fragrance use.
 
Recommendation for adenosine phosphate flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov:search
NLM Hazardous Substances Data Bank:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
Env. Mutagen Info. Center:Search
EPA Substance Registry Services (TSCA):61-19-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :6083
National Institute of Allergy and Infectious Diseases:Data
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyldihydrogen phosphate
Chemidplus:0000061198
 
References:
 [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyldihydrogen phosphate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:61-19-8
Pubchem (cid):6083
Pubchem (sid):134970876
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2009
(IUPAC):Atomic Weights of the Elements 2009 (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):C00020
HMDB (The Human Metabolome Database):HMDB00045
FooDB:FDB021806
YMDB (Yeast Metabolome Database):YMDB00097
ChemSpider:View
Wikipedia:View
RSC Learn Chemistry:View
EFSA Update of results on the monitoring of furan levels in food:Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:Read Report
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 biological additives
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 adenosine 5'-(dihydrogen phosphate)
 adenosine 5'-monophosphate
 adenosine 5'-monophosphoric acid
 adenosine 5'-phosphate
 adenosine 5'-phosphorate
 adenosine 5'-phosphoric acid
 adenosine monophosphate
5'-adenosine monophosphate
 adenosine-5'-monophosphate
 adenosine-5'-monophosphorate
 adenosine-5'-monophosphoric acid
 adenosine-5'-phosphate
 adenosine-5'P
 adenosine-monophosphate
 adenosine-phosphate
 adenovite
 adenyl
5'-adenylic acid, 8-amino-
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyldihydrogen phosphate
5'-AMP
 cardiomone
5'-deoxy-5'-thioadenosine 5'-monophosphate
 formycin 5'-monophosphate hydrate
 formycin 5'-phosphate
 lycedan
 muscle adenylate
 muscle adenylic acid
 muskeladenylsaeure
 my-B-den
 my-beta-den
 myoston
 phosphaden
5'-O-phosphonatoadenosine
5'-O-phosphonoadenosine
9H-purin-6-amine, 9-(5-O-phosphono-.beta.-D-ribofuranosyl)-
 vitamin B8
 
 
Notes:
adenylic acid. adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2'-, 3'-, or 5'-position. Adenosine monophosphate, also known as 5'-adenylic acid and abbreviated AMP, is a nucleotide that is found in RNA. It is an ester of phosphoric acid with the nucleoside adenosine. AMP consists of the phosphate group, the pentose sugar ribose, and the nucleobase adenine. AMP can be produced during ATP synthesis by the enzyme adenylate kinase. AMP has recently been approved as a 'Bitter Blocker' additive to foodstuffs. When AMP is added to bitter foods or foods with a bitter aftertaste it makes them seem 'sweeter'. This potentially makes lower calorie food products more palatable [HMDB]
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