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

5-hydroxypentanoic acid
valeric acid, 5-hydroxy-

Supplier Sponsors

CAS Number: 13392-69-3Picture of molecule3D/inchi
FDA UNII: H5EVV4LP59
Nikkaji Web:J140.264A
XlogP3:-0.10 (est)
Molecular Weight:118.13230000
Formula:C5 H10 O3
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
Boiling Point: 268.20 °C. @ 760.00 mm Hg (est)
Flash Point: 267.00 °F. TCC ( 130.30 °C. ) (est)
logP (o/w): -0.390 (est)
Soluble in:
 water, 6.792e+005 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.
5-Hydroxypentanoic Acid
 
Safety Information:
 
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 5-hydroxypentanoic acid usage levels up to:
 not for fragrance use.
 
Recommendation for 5-hydroxypentanoic acid flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :25945
National Institute of Allergy and Infectious Diseases:Data
5-hydroxypentanoic acid
Chemidplus:0013392693
 
References:
 5-hydroxypentanoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):25945
Pubchem (sid):134989612
 
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):C02804
HMDB (The Human Metabolome Database):HMDB61927
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
delta-hydroxypentanoic acid
5-hydroxyvaleric acid
 pentanoic acid, 5-hydroxy-
 valeric acid, 5-hydroxy-
 

Articles:

PubMed:Drought stress increases the production of 5-hydroxynorvaline in two C4 grasses.
PubMed:Effect of heat treatment on the antioxidant activity of extracts from citrus peels.
PubMed:Pregnane- and furostane-type oligoglycosides from the seeds of Allium tuberosum.
PubMed:A tertiary alcohol analog of gamma-hydroxybutyric acid as a specific gamma-hydroxybutyric acid receptor ligand.
PubMed:Anti-arthritic effects of the novel dipeptidyl peptidase IV inhibitors TMC-2A and TSL-225.
PubMed:Unusual dehydrations in anaerobic bacteria: considering ketyls (radical anions) as reactive intermediates in enzymatic reactions.
PubMed:Determination of valproic acid and its metabolites using gas chromatography with mass-selective detection: application to serum and urine samples from sheep.
PubMed:The identification of 5-hydroxy-L-norvaline in cultures of pyridoxine auxotrophs of Escherichia coli B.
PubMed:Studies on the renal transport of trimethylpentanoic acid metabolites of 2,2,4-trimethylpentane in rat renal cortical slices.
PubMed:Mechanism of action of an antifungal antibiotic, RI-331, (S) 2-amino-4-oxo-5-hydroxypentanoic acid; kinetics of inactivation of homoserine dehydrogenase from Saccharomyces cerevisiae.
PubMed:The mechanism of antifungal action of (S)-2-amino-4-oxo-5-hydroxypentanoic acid, RI-331: the inhibition of homoserine dehydrogenase in Saccharomyces cerevisiae.
PubMed:The mode of antifungal action of (S)2-amino-4-oxo-5-hydroxypentanoic acid, RI-331.
PubMed:Nucleoside phosphotransferase from malt sprouts. II. Studies on the active site and the phospho-intermediate.
PubMed:Direct chemical evidence for the mixed anhydride intermediate of carboxypeptidase A in ester and peptide hydrolysis.
PubMed:Mechanism of action of butyryl-CoA dehydrogenase: reactions with acetylenic, olefinic, and fluorinated substrate analogues.
PubMed:Metabolism of branched medium chain length fatty acid. II--beta-oxidation of sodium dipropylacetate in rats.
 
Notes:
None found
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