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

D-apiose

Supplier Sponsors

CAS Number: 639-97-4Picture of molecule3D/inchi
FDA UNII: E59T26TCEC
Nikkaji Web:J17.019D
MDL:MFCD08459679
XlogP3-AA:-3.10 (est)
Molecular Weight:150.13070000
Formula:C5 H10 O5
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
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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:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
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:
BOC Sciences
For experimental / research use only.
D-Apiose - Aqueous solution
Santa Cruz Biotechnology
For experimental / research use only.
D-Apiose
Sigma-Aldrich: Sigma
For experimental / research use only.
D-Apiose solution ≥99.0% (HPLC)
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:
natural substances and extractives
Recommendation for D-apiose usage levels up to:
 not for fragrance use.
 
Recommendation for D-apiose 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 :5460157
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(2R)-2,3,4-trihydroxy-3-(hydroxymethyl)butanal
Chemidplus:0000639974
 
References:
 (2R)-2,3,4-trihydroxy-3-(hydroxymethyl)butanal
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5460157
Pubchem (cas):639-97-4
 
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
KEGG (GenomeNet):C01488
HMDB (The Human Metabolome Database):HMDB29941
FooDB:FDB001214
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 parsley plant
Search Trop Picture
 
Synonyms:
3-C-hydroxymethyltetrose
(2R)-2,3,4-trihydroxy-3-(hydroxymethyl)butanal
 

Articles:

PubMed:Isotope Probing of the UDP-Apiose/UDP-Xylose Synthase Reaction: Evidence of a Mechanism via a Coupled Oxidation and Aldol Cleavage.
PubMed:Transcriptome-guided gene isolation and functional characterization of UDP-xylose synthase and UDP-D-apiose/UDP-D-xylose synthase families from Ornithogalum caudatum Ait.
PubMed:Two new compounds from the leaves of Indocalamus latifolius.
PubMed:A study of pharmacokinetic interactions among co-existing ingredients in Viscum coloratum after intravenous administration of three different preparations to rats.
PubMed:Hepatoprotective sesquiterpenes and rutinosides from Murraya koenigii (L.) Spreng.
PubMed:Analysis of UDP-D-apiose/UDP-D-xylose synthase-catalyzed conversion of UDP-D-apiose phosphonate to UDP-D-xylose phosphonate: implications for a retroaldol-aldol mechanism.
PubMed:cDNA-AFLP analysis on bolting or flowering of flowering Chinese cabbage and molecular characteristics of BrcuDFR-like/BrcuAXS gene.
PubMed:Simultaneous determination of ten flavonoids from Viscum coloratum grown on different host species and different sources by LC-MS.
PubMed:A fluoro analogue of UDP-α-D-glucuronic acid is an inhibitor of UDP-α-D-apiose/UDP-α-D-xylose synthase.
PubMed:Studies on the active components and antioxidant activities of the extracts of Mimosa pudica Linn. from southern China.
PubMed:Real-time NMR monitoring of intermediates and labile products of the bifunctional enzyme UDP-apiose/UDP-xylose synthase.
PubMed:Synthesis of 3'-deoxyapionucleoside triphosphates and their incorporation into DNA by DNA polymerase.
PubMed:Depletion of UDP-D-apiose/UDP-D-xylose synthases results in rhamnogalacturonan-II deficiency, cell wall thickening, and cell death in higher plants.
PubMed:Nucleotide sugar interconversions and cell wall biosynthesis: how to bring the inside to the outside.
PubMed:The biosynthesis of the branched-chain sugar d-apiose in plants: functional cloning and characterization of a UDP-d-apiose/UDP-d-xylose synthase from Arabidopsis.
PubMed:Structural studies of the pectic polysaccharide from duckweed Lemna minor L.
PubMed:[Structure and physiological activity of lemnan, Lemna minor L. pectin].
PubMed:Characterization of some O-acetylated saponins from Quillaja saponaria Molina.
PubMed:Triterpenoid saponins containing an acetylated branched D-fucosyl residue from Quillaja saponaria Molina.
PubMed:Conformationally constrained analogues of diacylglycerol having a perhydrofuro[3,4-c]furan-1,4-dione bis-gamma-butyrolactone skeleton.
PubMed:Conformationally constrained analogues of diacylglycerol. 13. Protein kinase C ligands based on templates derived from 2,3-dideoxy-L-erythro(threo)-hexono-1,4-lactone and 2-deoxyapiolactone.
PubMed:Synthesis of bis-gamma-butyrolactones containing conformationally constrained (S)- and (R)-diacylglycerol structures.
PubMed:Developmental Control of Apiogalacturonan Biosynthesis and UDP-Apiose Production in a Duckweed.
PubMed:Conversion of UDP-D-glucuronic acid to UDP-D-apiose and UDP-D-xylose by an enzyme isolated from Lemna minor.
PubMed:Synthesis, characterization and properties of uridine 5'-( -D-apio-D-furanosyl pyrophosphate).
PubMed:[Biosynthesis of D-apiose and D-xylose in parsley and Lemma minor and their regulation through light].
PubMed:Proof for the origin of the branch hydroxymethyl carbon of D-apiose from carbon 3 of D-glucuronic acid.
PubMed:Synthesis of 3-C-hydroxymethyl-1,2-O-isopropylidene- -D-erythrofuranose and D-apiose.
PubMed:Biosynthesis of D-apiose. V. NAD+-dependent biosynthesis of UDP-apiose and UDP-xylose from UDP-D-glucuronic acid with an enzyme preparation from Lemna minor L.
PubMed:D-apiose reductase from Aerobacter aerogenes.
PubMed:Isolation and partial characterization of apiogalacturonans from the cell wall of Lemna minor.
PubMed:Biosynthesis of D-apiose in a cell-free system from Lemna minor L.
PubMed:Biosynthesis of D-apiose. IV. Formation of UDP-apiose from UDP-D-glucuronic acid in cell-free extracts of parsley (Apium petroselinum L.) and Lemna minor.
PubMed:Inositol Metabolism in Plants. IV. Biosynthesis of Apiose in Lemna and Petroselinum.
PubMed:The biosynthesis of D-apiose in Lemna minor.
PubMed:THE BIOSYNTHESIS OF THE BRANCHED CHAIN SUGAR D-APIOSE IN LEMNA AND PARSLEY.
 
Notes:
None found
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