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

meso-tartaric acid
butanedioic acid, 2,3-dihydroxy-, (2R,3S)-

Supplier Sponsors

Name:(2R,3S)-2,3-dihydroxybutanedioic acid
CAS Number: 147-73-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:205-696-1
FDA UNII: JQO211TF1A
Nikkaji Web:J134.706C
XlogP3:-1.90 (est)
Molecular Weight:150.08702000
Formula:C4 H6 O6
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:flavoring agents
 
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
FEMA Number:3044 meso-tartaric acid
FDA:No longer provide for the use of these seven synthetic flavoring substances
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 147.00 °C. @ 760.00 mm Hg
Soluble in:
 water, 5.60E+05 mg/L @ 20 °C (exp)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
meso-Tartaric 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:
flavoring agents
Recommendation for meso-tartaric acid usage levels up to:
 not for fragrance use.
 
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -1300.00000
beverages(nonalcoholic): -960.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -3700.00000
condiments / relishes: -10000.00000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -570.00000
fruit ices: -570.00000
gelatins / puddings: -60.00000
granulated sugar: --
gravies: --
hard candy: -5400.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):147-73-9
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :447315
National Institute of Allergy and Infectious Diseases:Data
(2R,3S)-2,3-dihydroxybutanedioic acid
Chemidplus:0000147739
 
References:
 (2R,3S)-2,3-dihydroxybutanedioic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):447315
Pubchem (sid):135034978
 
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):C00552
HMDB (The Human Metabolome Database):Search
FDA Listing of Food Additive Status:View
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 butanedioic acid, 2,3-dihydroxy-, (2R,3S)-
(2R,3S)-2,3-dihydroxybutanedioic acid
 mesotartaric acid
(2R,3S)-tartaric acid
(R,S)-tartaric acid
 

Articles:

PubMed:Synthesis and the absolute configuration of both enantiomers of 4,5-dihydroxy-3-(formyl)cyclopent-2-enone acetonide as a new chiral building block for prostanoid synthesis.
PubMed:Synthesis of tartaric acid analogues of FR258900 and their evaluation as glycogen phosphorylase inhibitors.
PubMed:Isolation of rotational isomers and developments derived therefrom.
PubMed:Phase selection and energetics in chiral alkaline Earth tartrates and their racemic and meso analogues: synthetic, structural, computational, and calorimetric studies.
PubMed:Dicarboxylic acid esters as transdermal permeation enhancers: effects of chain number and geometric isomers.
PubMed:Phenolic compounds in field horsetail (Equisetum arvense L.) as natural antioxidants.
PubMed:Role of the gauche effect and local 1,3-dipole-dipole interactions in stabilizing an unusual conformation of tartarodinitriles.
PubMed:A novel highly acidic polysaccharide with inhibitory activity on calcification from the calcified scale "coccolith" of a coccolithophorid alga, Pleurochrysis haptonemofera.
PubMed:Surface chirality of CuO thin films.
PubMed:[Vasorelaxant activity of caffeic acid derivatives from Cichorium intybus and Equisetum arvense].
PubMed:Chiral quantification of D-, L-, and meso-tartaric acid mixtures using a mass spectrometric kinetic method.
PubMed:Synthesis and conformational analysis of small peptides containing 6-endo-BT(t)L scaffolds as reverse turn mimetics.
PubMed:Depsipeptide dendrimers.
PubMed:Introduction of the new dipeptide isostere 7-endo-BtA as reverse turn inducer in a Bowman-Birk proteinase inhibitor: synthesis and conformational analysis.
PubMed:Studies toward the synthesis of pinolidoxin, a phytotoxic nonenolide from the fungus Ascochyta pinodes. Determination of the configuration at the C-7, C-8, and C-9 chiral centers and stereoselective synthesis of the C(6)-C(18) fragment.
PubMed:Candida tartarivorans sp. nov., an anamorphic ascomycetous yeast with the capacity to degrade L(+)- and meso-tartaric acid.
PubMed:The reaction of hyaluronic acid and its monomers, glucuronic acid and N-acetylglucosamine, with reactive oxygen species.
PubMed:Electron microscopic study of supramolecular liquid crystalline polymers formed by molecular-recognition-directed self-assembly from complementary chiral components.
PubMed:Utilization of tartaric acid and related compounds by yeasts: taxonomic implications.
PubMed:Purification, characterization and preliminary X-ray study of fumarase from Saccharomyces cerevisiae.
PubMed:A rheological study of the role of additives on the setting of glass-ionomer cements.
PubMed:Purification and characterization of hydroxycinnamoyl D-glucose. Quinate hydroxycinnamoyl transferase in the root of sweet potato, Ipomoea batatas Lam.
PubMed:D-Malic enzyme of Pseudomonas fluorescens.
PubMed:Stereoisomeric Characterization of Tartaric Acid Produced during l-Ascorbic Acid Metabolism in Plants.
PubMed:p-Coumaroyl-meso-tartaric acid from spinach chloroplast preparations.
 
Notes:
None found
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