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

hydroxypyruvaldehyde
pyruvaldehyde, hydroxy-

Supplier Sponsors

Name:3-hydroxy-2-oxopropanal
CAS Number: 997-10-4Picture of molecule3D/inchi
FDA UNII: NE0T88WG0M
Nikkaji Web:J396.558I
Beilstein Number:1901779
XlogP3-AA:-1.00 (est)
Molecular Weight:88.06248000
Formula:C3 H4 O3
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
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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:colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 175.00 to 176.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.353000 mmHg @ 25.00 °C. (est)
Flash Point: 166.00 °F. TCC ( 74.20 °C. ) (est)
logP (o/w): -1.253 (est)
Soluble in:
 water, 1e+006 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Aston Chemical
For experimental / research use only.
Hydroxypyruvaldehyde
BOC Sciences
For experimental / research use only.
Varenicline Impurity 12 98%
 
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:
natural substances and extractives
Recommendation for hydroxypyruvaldehyde usage levels up to:
 not for fragrance use.
 
Recommendation for hydroxypyruvaldehyde 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 :101392
National Institute of Allergy and Infectious Diseases:Data
3-hydroxy-2-oxopropanal
Chemidplus:0000997104
 
References:
 3-hydroxy-2-oxopropanal
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):101392
Pubchem (sid):135058970
 
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
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 wine
Search Picture
 
Synonyms:
 acrolein, 2,3-dihydroxy-
2,3-dihydroxyacrolein
3-hydroxy-2-oxopropanal
 propanal, 3-hydroxy-2-oxo-
 pyruvaldehyde, hydroxy-
 

Articles:

PubMed:Free α-dicarbonyl compounds in coffee, barley coffee and soy sauce and effects of in vitro digestion.
PubMed:Na+/H+ exchanger 1 inhibition reverses manifestation of peripheral diabetic neuropathy in type 1 diabetic rats.
PubMed:Classification and characterization of manuka honeys based on phenolic compounds and methylglyoxal.
PubMed:Increased glyoxalase I levels inhibit accumulation of oxidative stress and an advanced glycation end product in mouse mesangial cells cultured in high glucose.
PubMed:Human aldo-keto reductase AKR7A2 protects against the cytotoxicity and mutagenicity of reactive aldehydes and lowers intracellular reactive oxygen species in hamster V79-4 cells.
PubMed:Overexpression of glyoxalase-I reduces hyperglycemia-induced levels of advanced glycation end products and oxidative stress in diabetic rats.
PubMed:Degradation of glucose: reinvestigation of reactive alpha-Dicarbonyl compounds.
PubMed:Organocatalysis with endogenous compounds: towards novel non-enzymatic reactions.
PubMed:Formation of 2,5-dimethyl-4-hydroxy-3(2H)-furanone through methylglyoxal: a Maillard reaction intermediate.
PubMed:Investigations on the promoting effect of ammonium hydrogencarbonate on the formation of acrylamide in model systems.
PubMed:Methylglyoxal in food and living organisms.
PubMed:Heat-shock protein 27 is a major methylglyoxal-modified protein in endothelial cells.
PubMed:Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dGuo adducts.
PubMed:A copper chelating agent suppresses carbonyl stress in diabetic rat lenses.
PubMed:In vivo prooxidant state in Werner syndrome (WS): results from three WS patients and two WS heterozygotes.
PubMed:Mechanism of the inhibitory effect of OPB-9195 [(+/-)-2-isopropylidenehydrazono-4-oxo-thiazolidin-5-yla cetanilide] on advanced glycation end product and advanced lipoxidation end product formation.
PubMed:Origin of carbohydrate degradation products in L-Alanine/D-[(13)C]glucose model systems.
PubMed:Trioses and related substances: tools for the study of pancreatic beta-cell function.
PubMed:A systematic approach to evaluate the modification of lens proteins by glycation-induced crosslinking.
PubMed:N2,7-bis(1-hydroxy-2-oxopropyl)-2'-deoxyguanosine: identical noncyclic adducts with 1,3-dichloropropene epoxides and methylglyoxal.
PubMed:Overexpression of glyoxalase-I in bovine endothelial cells inhibits intracellular advanced glycation endproduct formation and prevents hyperglycemia-induced increases in macromolecular endocytosis.
PubMed:Protein modification by methylglyoxal: chemical nature and synthetic mechanism of a major fluorescent adduct.
PubMed:Inactivation of glutathione reductase by 4-hydroxynonenal and other endogenous aldehydes.
PubMed:Oxidative inhibition of red blood cell ATPases by glyceraldehyde.
PubMed:Effects of derivatives of hydroxypyruvaldehyde phenylosazone on the Ca2+-adenosine triphosphatase activity of porcine erythrocyte membrane.
PubMed:Red blood cell oxidative metabolism induced by hydroxypyruvaldehyde.
PubMed:Effects of derivatives of hydroxypyruvaldehyde phenylosazone on bovine erythrocyte membrane. II. Stabilization of sphingomyelinase C-treated or untreated cells examined by coil planet centrifugation and electron microscopy.
PubMed:The autoxidation of glyceraldehyde and other simple monosaccharides under physiological conditions catalysed by buffer ions.
PubMed:The oxidation of oxyhaemoglobin by glyceraldehyde and other simple monosaccharides.
PubMed:Effects of derivatives of hydroxypyruvaldehyde phenylosazone on bovine erythrocyte membrane. I. Influence on the osmotic fragility and morphology.
PubMed:Formation of hydroxypyruvaldehyde phosphate in human erythrocytes.
PubMed:Oxidation of the carbanion intermediate of transaldolase by hexacyanoferrate (III).
PubMed:Specific irreversible inhibition of enzymes concomitant to the oxidation of carbanionic enzyme-substrate intermediates by hexacyanoferrate (III).
PubMed:Substrate activity of structural analogs of isocitrate for isocitrate dehydrogenases from bovine heart.
PubMed:Reaction of the carbanionic aldolase-substrate intermediate with tetranitromethane. Identification of the products, hydroxypyruvaldehyde phosphate and D-5-ketofructose 1,6-diphosphate.
 
Notes:
None found
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