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

adenosine
6-amino-9-b-D-ribofuranosyl-9H-purine

Sponsors

Name: (2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
CAS Number: 58-61-7Picture of molecule3D/inchi
Other: 46946-45-6
ECHA EINECS - REACH Pre-Reg: 200-389-9
FDA UNII: K72T3FS567
Nikkaji Web: J4.501B
Beilstein Number: 093029
XlogP3: -1.10 (est)
Molecular Weight: 267.24541000
Formula: C10 H13 N5 O4
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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 235.50 °C. @ 760.00 mm Hg
Boiling Point: 676.27 °C. @ 760.00 mm Hg (est)
Flash Point: 685.00 °F. TCC ( 362.80 °C. ) (est)
logP (o/w): -0.755 (est)
Soluble in:
 water, 8228 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 98% by HPLC
Changzhou Longo Chemical
Adenosine
Coompo
For experimental / research use only.
Adenosine from Plants ≥96%
George Uhe Company
Adenosine
Jiangyin Healthway
Adenosine
New functional food ingredients
Santa Cruz Biotechnology
For experimental / research use only.
Adenosine ≥99%
Sigma-Aldrich: Sigma
For experimental / research use only.
Adenosine ≥99%
 
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-man TDLo 50 ug/kg/1M-I
LUNGS, THORAX, OR RESPIRATION: BRONCHIOLAR CONSTRICTION
Human & Experimental Toxicology. Vol. 13, Pg. 263, 1994.

intravenous-man TDLo 143 ug/kg/I
SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE BEHAVIORAL: HEADACHE
Medical Journal of Australia.

intravenous-man TDLo 171 ug/kg
CARDIAC: PULSE RATE BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: COMA
American Journal of Emergency Medicine. Vol. 11, Pg. 192, 1993.

intravenous-man TDLo 257 ug/kg
CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP LUNGS, THORAX, OR RESPIRATION: CYANOSIS
American Journal of Emergency Medicine. Vol. 11, Pg. 249, 1993.

intravenous-man TDLo 257 ug/kg/1D-I
CARDIAC: CHANGE IN RATE VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION CARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION)
Annals of Internal Medicine. Vol. 122, Pg. 351, 1995.

intraperitoneal-mouse LD50 500 mg/kg
National Technical Information Service. Vol. AD277-689

oral-mouse LD50 > 20000 mg/kg
Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 8, Pg. 45, 1980.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: cosmetic ingredient for skin conditioning
Recommendation for adenosine usage levels up to:
 not for fragrance use.
 
Recommendation for adenosine flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov: search
Daily Med: search
NLM Hazardous Substances Data Bank: Search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
Env. Mutagen Info. Center: Search
EPA Substance Registry Services (TSCA): 58-61-7
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 60961
National Institute of Allergy and Infectious Diseases: Data
 (2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
Chemidplus: 0000058617
RTECS: AU7175000 for cas# 58-61-7
 
References:
 (2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 58-61-7
Pubchem (cid): 60961
Pubchem (sid): 135017562
 
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): C00212
HMDB (The Human Metabolome Database): HMDB00050
FooDB: FDB003554
YMDB (Yeast Metabolome Database): YMDB00058
Export Tariff Code: 2934.90.5000
MedlinePlusSupp: View
VCF-Online: VCF Volatile Compounds in Food
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
Formulations/Preparations:
•boniton •myocol •nucleocardyl •sandesin
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other): note
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Synonyms:
(-)-adenosine
b-D-adenosine
6-amino-9-b-D-ribofuranosyl-9H-purine
(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydro-3,4-furandiol
(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxyméthyl)tétrahydrofurane-3,4-diol
(2R,3R,4S,5R)-2-(6-amino-purin-9-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
 myocol
 nucleocardyl
9-b-D-ribofuranosidoadenine
9-b-D-ribofuranosyl-9H-purin-6-amine
 
 
Notes:
a nucleoside that is composed of adenine and d-ribose. adenosine or adenosine derivatives play many important biological roles in addition to being components of dna and rna. adenosine itself is a neurotransmitter. Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety via a beta-N9-glycosidic bond. [Wikipedia]
 
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