Skip to Content
Merck
All Photos(3)

Documents

T400

Sigma-Aldrich

DL-Tartaric acid

ReagentPlus®, 99%

Synonym(s):

DL-2,3-Dihydroxybutanedioic acid

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
HOOC(CHOH)2COOH
CAS Number:
133-37-9
Molecular Weight:
150.09
Beilstein:
1725148
EC Number:
205-105-7
MDL number:
MFCD00071626
UNSPSC Code:
12352100
PubChem Substance ID:
24900184
NACRES:
NA.22

product line

ReagentPlus®

Assay

99%

mp

210-212 °C (lit.)

SMILES string

O[C@@H]([C@H](O)C(O)=O)C(O)=O

InChI

1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m0/s1

InChI key

FEWJPZIEWOKRBE-LWMBPPNESA-N

Looking for similar products? Visit Product Comparison Guide

Application

DL-Tartaric acid can be used:
  • In the Debus–Radziszewski reaction as a weak acid for the synthesis of imidazolium ionic liquid.
  • As an additive in electrochemical deposition technique for the synthesis of bismuth thin films to be used as X-ray absorbers.
  • As a complexing agent for the synthesis of nano-crystalline indium tin oxide (ITO) powder.
  • As a dopant for the synthesis of polyaniline nanofibers and nanotubes by oxidation polymerization.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

410.0 °F - closed cup

Flash Point(C)

210 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Transparent and conducting ITO thin films by spin coating of an aqueous precursor solution.
Sunde TOL, et al.
Journal of Materials Chemistry, 22(31), 15740-15749 (2012)
Microstructure and electrical transport in electrodeposited Bi films.
Moral-Vico J, et al.
Journal of Electroanalytical Chemistry, 832(49), 40-47 (2019)
The unique role of DL-tartaric acid in determining the morphology of polyaniline nanostructures during an interfacial oxidation polymerization.
Sun Q and Deng Y
Materials Letters, 62(12-13), 1831-1834 (2008)
Green Imidazolium Ionics-From Truly Sustainable Reagents to Highly Functional Ionic Liquids.
Troger-M?ller S, et al.
Chemistry?A European Journal , 23(49), 11810-11817 (2017)
J B Olivato et al.
Carbohydrate polymers, 92(2), 1705-1710 (2013-02-13)
Tartaric acid (TA), a dicarboxylic acid, can act as a compatibiliser in starch/polyester blends. A mixture design was proposed to evaluate the effect of TA on the properties of starch/poly (butylene adipate co-terephthalate) (PBAT) blown films plasticised with glycerol. The
View All Related Papers

Chromatograms

application for HPLC

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service