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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
Vitreous concentration of topically applied brimonidine tartrate 0.2%.
2001 Apr
Synthesis and evaluation of a C-glycosyl nucleoside as an inhibitor of chitin synthase.
2001 Aug 30
A comparison of salts for the crystallization of macromolecules.
2001 Feb
Response charactterization of ammonium tartrate solid state pellets for ESR dosimetry with radiotherapeutic photon and electron beams.
2001 Feb
Sarcosinium tartrate.
2001 Feb
Determination of organic acids of low molecular weight and phosphate in soil by capillary electrophoresis.
2001 Jul-Aug
Chemical and biochemical issues related to X-ray crystallography of the ligand-binding domain of estrogen receptor alpha.
2001 May-Jun
Technetium-99m direct radiolabeling of lanreotide: a somatostatin analog.
2001 Nov
Direct chiral resolution of malic acid in apple juice by ligand-exchange capillary electrophoresis using copper(II)-L-tartaric acid as a chiral selector.
2001 Sep
Oxidation of hydroquinones by the versatile ligninolytic peroxidase from Pleurotus eryngii. H2O2 generation and the influence of Mn2+.
2001 Sep
The MRP1-mediated effluxes of arsenic and antimony do not require arsenic-glutathione and antimony-glutathione complex formation.
2002 Apr
New materials for ESR dosimetry.
2002 Apr
Chiral versus racemic building blocks in supramolecular chemistry: tartrate salts of organic diamines.
2002 Apr
Thermophysical properties of pharmaceutically compatible buffers at sub-zero temperatures: implications for freeze-drying.
2002 Feb
The microphthalmia transcription factor and the related helix-loop-helix zipper factors TFE-3 and TFE-C collaborate to activate the tartrate-resistant acid phosphatase promoter.
2002 Feb
Screening method for inherited disorders of purine and pyrimidine metabolism by capillary electrophoresis with reversed electroosmotic flow.
2002 Feb 15
Selective estrogen receptor modulators as a new therapeutic drug group: concept to reality in a decade.
2002 Jan
Therapy and disease concepts: the history (and future?) of antimony in cancer.
2002 Jan
Crystal structure analysis of the exocytosis-sensitive phosphoprotein, pp63/parafusin (phosphoglucomutase), from Paramecium reveals significant conformational variability.
2002 Jan 11
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
High frequency of phenotypic deviations in Physcomitrella patens plants transformed with a gene-disruption library.
2002 Jul 18
Engineering the substrate specificity of D-amino-acid oxidase.
2002 Jul 26
Improving the labeling of S-acetyl NHS-MAG(3)-conjugated morpholino oligomers.
2002 Jul-Aug
Effects of cyclic pressure on bone marrow cell cultures.
2002 Jun
Dissociation of angiogenesis and osteoclastogenesis during endochondral bone formation in neonatal mice.
2002 Jun
Stereoselective radical reactions of some tartaric and glyceric acid derivatives.
2002 Jun 13
Determination of the side-products formed during the nitroxide-mediated bleach oxidation of glucose to glucaric acid.
2002 Jun 5
Recruitment, augmentation and apoptosis of rat osteoclasts in 1,25-(OH)2D3 response to short-term treatment with 1,25-dihydroxyvitamin D3 in vivo.
2002 Jun 7
Use of disposable GRC electrodes for the detection of phenol and chlorophenols in liquid chromatography.
2002 May
Potassium antimonyl tartrate induces reactive oxygen species-related apoptosis in human myeloid leukemic HL60 cells.
2002 May
Synovial macrophage-osteoclast differentiation in inflammatory arthritis.
2002 Oct
Ectonucleotide diphosphohydrolase activity in Crithidia deanei.
2002 Oct
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
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
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