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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H4O6.2Na
Molecular Weight 194.0505
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM TARTRATE

SMILES

[Na+].[Na+].O[C@H]([C@@H](O)C([O-])=O)C([O-])=O

InChI

InChIKey=HELHAJAZNSDZJO-OLXYHTOASA-L
InChI=1S/C4H6O6.2Na/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);;/q;2*+1/p-2/t1-,2-;;/m1../s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H4O6
Molecular Weight 148.071
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Tartaric acid is found in many plants such as grapes, tamarinds, pineapples, mulberries and so on. Wine lees (called mud in the US), the sediment collected during the fermentation of grapes, contains potassium bitartrate (potassium hydrogen tartrate) as its major component. L-(+)-tartaric acid is an enantiomer of tartaric acid. Twenty five years before the tetrahedral structure for carbon was proposed in 1874 to explain the optical activity and other properties of organic compounds, Louis Pasteur discovered the existence of enantiomerism in tartaric acid. L-(+)-tartaric acid is widely used in food and beverage as acidity regulator with E number E334.

Originator

Curator's Comment: Scheele first prepared tartaric acid. Louis Pasteur discovered the existence of enantiomerism in tartaric acid

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Inactive ingredient
CLEARASIL DAILY CLEAR CLEAR SKIN

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Synthesis and evaluation of a C-glycosyl nucleoside as an inhibitor of chitin synthase.
2001 Aug 30
Production and chemiluminescent free radical reactions of glyoxal in lipid peroxidation of linoleic acid by the ligninolytic enzyme, manganese peroxidase.
2001 Dec
A comparison of salts for the crystallization of macromolecules.
2001 Feb
Sarcosinium tartrate.
2001 Feb
Reversal of multidrug resistance-associated protein-mediated drug resistance in cultured human neuroblastoma cells by the quinolone antibiotic difloxacin.
2001 Jan
Comparison of the clinical success and quality-of-life impact of brimonidine 0.2% and betaxolol 0.25 % suspension in patients with elevated intraocular pressure.
2001 Jul
Malo-ethanolic fermentation in grape must by recombinant strains of Saccharomyces cerevisiae.
2001 Jul
Isolation and characterization of Mn(III) tartrate from Phanerochaete chrysosporium culture broth.
2001 Jul 24
Determination of organic acids of low molecular weight and phosphate in soil by capillary electrophoresis.
2001 Jul-Aug
Catalytic spectrophotometric determination of vanadium in seawaters based on the bromate oxidative coupling reaction of metol and 2,3,4-trihydroxybenzoic acid.
2001 Jun
Chiral separations of transition metal complexes using capillary zone electrophoresis.
2001 Jun 15
Mutation of a single conserved tryptophan in multidrug resistance protein 1 (MRP1/ABCC1) results in loss of drug resistance and selective loss of organic anion transport.
2001 May 11
[Acid phosphatase, ACP (EC 3.1.3.2)].
2001 Nov
Technetium-99m direct radiolabeling of lanreotide: a somatostatin analog.
2001 Nov
Novel bicistronic retroviral vector expressing gamma-glutamylcysteine synthetase and the multidrug resistance protein 1 (MRP1) protects cells from MRP1-effluxed drugs and alkylating agents.
2001 Sep 20
Preformulation studies for an ultrashort-acting neuromuscular blocking agent GW280430A. I. Buffer and cosolvent effects on the solution stability.
2002
The MRP1-mediated effluxes of arsenic and antimony do not require arsenic-glutathione and antimony-glutathione complex formation.
2002 Apr
The structure and mechanism of the type II dehydroquinase from Streptomyces coelicolor.
2002 Apr
Stereoselective synthesis of myo-inositol via ring-closing metathesis: a building block for glycosylphosphatidylinositol (GPI) anchor synthesis.
2002 Apr 18
Towards atomic resolution with crystals grown in gel: the case of thaumatin seen at room temperature.
2002 Aug 1
Thermophysical properties of pharmaceutically compatible buffers at sub-zero temperatures: implications for freeze-drying.
2002 Feb
Ergotamine-induced anorectal strictures: report of five cases.
2002 Feb
Revision of absolute configuration of enantiomeric (methylenecyclopropyl)carbinols obtained from (R)-(-)- and (S)-(+)-epichlorohydrin and methylenetriphenylphosphorane. Implications for reaction mechanism and improved synthesis of antiviral methylenecyclopropane analogues of nucleosides.
2002 Jan 11
Effect of antibiotics on in vitro and in vivo avian cartilage degradation.
2002 Jan-Mar
Improving the labeling of S-acetyl NHS-MAG(3)-conjugated morpholino oligomers.
2002 Jul-Aug
Dissociation of angiogenesis and osteoclastogenesis during endochondral bone formation in neonatal mice.
2002 Jun
Consumption of an omega-3 fatty acids product, INCELL AAFA, reduced side-effects of CPT-11 (irinotecan) in mice.
2002 Mar 18
Potassium antimonyl tartrate induces reactive oxygen species-related apoptosis in human myeloid leukemic HL60 cells.
2002 May
Formation of methylantimony species by an aerobic prokaryote: Flavobacterium sp.
2002 Oct
Development of high-affinity ligands and photoaffinity labels for the D-fructose transporter GLUT5.
2002 Oct 15
Symmetric and helical growth of polyacetylene fibers over a single copper crystal derived from copper tartrate decomposition.
2002 Sep 5
Patents

Sample Use Guides

L-(+)-tartaric acid as a food additive. Acceptable Daily Intake: 0-30 mg/kg
Route of Administration: Oral
In Vitro Use Guide
After incubation in medium containing 50 mM L(+)-tartaric acid, osteoclasts and chondroclasts were heavily stained with reaction product.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:10:24 GMT 2023
Edited
by admin
on Fri Dec 15 15:10:24 GMT 2023
Record UNII
QTO9JB4MDD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SODIUM TARTRATE
FCC   II   MART.   MI   WHO-DD  
Systematic Name English
DISODIUM L-TARTRATE
Systematic Name English
SODIUM TARTRATE [MI]
Common Name English
INS-335(II)
Code English
DISODIUM TARTRATE [INCI]
Common Name English
SODIUM DEXTRO-TARTRATE
Common Name English
BUTANEDIOIC ACID, 2,3-DIHYDROXY- (2R,3R)-, DISODIUM SALT
Common Name English
SODIUM TARTRATE [FCC]
Common Name English
SODIUM (+)-TARTRATE
Systematic Name English
Sodium tartrate [WHO-DD]
Common Name English
E-335(II)
Code English
DISODIUM (+)-2,3-DIHYDROXYBUTANEDIOIC ACID
Systematic Name English
DISODIUM TARTRATE
INCI  
INCI  
Official Name English
INS NO.335(II)
Code English
SODIUM TARTRATE, L (+)-
Common Name English
SODIUM TARTRATE [MART.]
Common Name English
TARTARIC ACID, DISODIUM SALT
Common Name English
SODIUM TARTRATE [II]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION INS-335(II)
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
CFR 21 CFR 184.1801
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
CFR 21 CFR 331.11
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
WHO-VATC QA06AD21
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
WHO-ATC A06AD21
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
CFR 21 CFR 331.15
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
CODEX ALIMENTARIUS (GSFA) INS-335(II)
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
Code System Code Type Description
MERCK INDEX
m10082
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY Merck Index
RXCUI
56524
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY RxNorm
DRUG BANK
DB13707
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID2057861
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
FDA UNII
QTO9JB4MDD
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
EVMPD
SUB15327MIG
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
SMS_ID
100000078124
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
WIKIPEDIA
SODIUM TARTRATE
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
NCI_THESAURUS
C45678
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
CONCEPT Industrial Aid
DRUG CENTRAL
4780
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PRIMARY
PUBCHEM
162637
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107781
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
CAS
868-18-8
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
MESH
C029768
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
NCI_THESAURUS
C77502
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
CHEBI
63017
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
DAILYMED
QTO9JB4MDD
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-773-3
Created by admin on Fri Dec 15 15:10:25 GMT 2023 , Edited by admin on Fri Dec 15 15:10:25 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE