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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-OTWIGTIJSA-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-;;/m0../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

Description
Curator's Comment: The description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/11149858 | http://www.inchem.org/documents/jecfa/jecmono/v05je93.htm

D-(-)-tartaric acid is isomer of tartaric acid, that industrially produced in the largest amounts. D-(-)-Tartaric acid may be used in the preparation of enantiospecific homochiral cis-4-formyl β-lactams. It may also be used as a starting material in the synthesis of D-erythro-sphingosine and L-lyxo-phytosphingosine. D-(-)-tartaric acid is widely used as an acidizing agent for beverages and other foods, and this use is similar to citric acid. Tartaric acid can be used as an acid dye mordant when it is combined with tannin. It is also used for some development and fixing operations in the photographic industry. D-(-)-Tartaric Acid is used in the preparation of synthetic analgesics. Tartaric acid is metabolically inert in the human body. When taken by mouth, only about 20% of ingested tartrate is eliminated in the urine; the remainder is not absorbed as such since it is destroyed in the intestinal tract by bacterial action. Sodium tartrate in daily doses of up to 10 or even 20 g has been used in medical practice as a laxative.

Originator

Sources: Zeitschrift fuer Anorganische und Allgemeine Chemie (1928), 169, 161-72. CODEN:ZAACAB ISSN:0044-2313.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
An efficient and convenient approach to the total synthesis of sphingofungin.
2000 Dec 29
Patents

Patents

Sample Use Guides

Sodium tartrate in daily doses of up to 10 or even 20 g has been used in medical practice as a laxative.
Route of Administration: Oral
The transepithelial transport ofRhol23 in rat colon was examined using diffusion chamber method. The serosal and mucosal reservoirs were filled with 5 ml. Krebs Henseleit bicarbonate buffer (KHBB) solution, which was continuously circulated and oxygenated by mixed gas (95% 02/5% C02) to maintain tissue viability at pH 7.4 and 37°C throughout the experiments. After 20 min, the KHBB solution was exchanged with 5 ml. KHBB solution containing Rhol23 in the serosal side (donor side) and with 5 ml. KHBB solution without Rhol23 in the mucosal side (acceptor side). In the same experiments, Rhol23 was added to the mucosal side (donor side) but not to the serosal side (acceptor side). To examine the effect of TA (D-(-)-tartaric acid), the mucosal reservoir was filled with KHBB solution containing TA (5 or 10 mM). The pH of KHBB solution containing TA was adjusted to 7.4 using sodium hydroxide. The samples were taken from the acceptor side at intervals of 10 min. Permea¬tion clearance (CLp) was obtained as follows.
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:39:39 GMT 2023
Edited
by admin
on Sat Dec 16 08:39:39 GMT 2023
Record UNII
L134I28UJY
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM TARTRATE, (-)-
Systematic Name English
DISODIUM TARTRATE, (-)-
Common Name English
BUTANEDIOIC ACID, 2,3-DIHYDROXY-, DISODIUM SALT, (2S,3S)-
Systematic Name English
BUTANEDIOIC ACID, 2,3-DIHYDROXY-, SODIUM SALT (1:2), (2S,3S)-
Systematic Name English
TARTARIC ACID, SODIUM SALT, D-
Common Name English
SODIUM D-TARTRATE
Systematic Name English
BUTANEDIOIC ACID, 2,3-DIHYDROXY-, DISODIUM SALT, (S-(R*,R*))-
Systematic Name English
DISODIUM (-)-TARTRATE
Systematic Name English
DISODIUM D-TARTRATE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 331.11
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
CFR 21 CFR 331.15
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
244-213-9
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
PRIMARY
PUBCHEM
159905
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID50943433
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
PRIMARY
CAS
21106-15-0
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
NON-SPECIFIC STOICHIOMETRY
FDA UNII
L134I28UJY
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
PRIMARY
CAS
109175-69-1
Created by admin on Sat Dec 16 08:39:39 GMT 2023 , Edited by admin on Sat Dec 16 08:39:39 GMT 2023
PRIMARY