251380

Sigma-Aldrich

L-(+)-Tartaric acid

ACS reagent, ≥99.5%

Synonym(s):
L-Threaric acid, (2R,3R)-(+)-Tartaric acid
Linear Formula:
HO2CCH(OH)CH(OH)CO2H
CAS Number:
Molecular Weight:
150.09
Beilstein/REAXYS Number:
1725147
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

grade

ACS reagent

vapor density

5.18 (vs air)

assay

≥99.5%

form

crystalline powder
crystals

optical activity

[α]20/D +12.4°, c = 20 in H2O

optical purity

ee: 99% (GLC)

autoignition temp.

797 °F

impurities

≤0.002% S compounds
≤0.005% insolubles

ign. residue

≤0.02%

mp

170-172 °C (lit.)

anion traces

chloride (Cl-): ≤0.001%
oxalate (C2O42-): passes test
phosphate (PO43-): ≤0.001%

cation traces

Fe: ≤5 ppm
heavy metals (as Pb): ≤5 ppm

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-/m1/s1

InChI key

FEWJPZIEWOKRBE-JCYAYHJZSA-N

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Application

L-(+)-Tartaric acid may be used in the synthesis of (R,R)-1,2-diammoniumcyclohexane mono-(+)-tartrate, an intermediate to prepare an enantioselective epoxidation catalyst. It may also be used as a starting material in the multi-step synthesis of 1,4-di-O-benzyl-L-threitol. It can be used a chiral resolving agent for the resolution of 2,2′-bispyrrolidine.
Chiral building block for natural products. Also forms a Diels-Alder catalyst with TiCl2(O-i-Pr)2.

Packaging

2.5 kg in poly bottle
5 g in glass bottle
100, 500 g in poly bottle

pictograms

Corrosion

signalword

Danger

hcodes

hazcat

Eye Dam. 1

storage_class_code

13 - Non Combustible Solids

WGK Germany

WGK 1

Flash Point F

302.0 °F - closed cup

Flash Point C

150 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

(R,R)-2,2'-bispyrrolidine and (S,S)-2,2'-bispyrrolidine: useful ligands for asymmetric synthesis
Denmark SE, et al.
Organic Syntheses, 83, 121-121 (2006)
(R,R)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamino manganese(iii) chloride, a highly enantioselective epoxidation catalyst
Jay F. Larrow and Eric N. Jacobsen
Organic Syntheses, 75, 1-1 (1998)
1,4-Di-O-alkyl threitols from tartaric acid: 1,4-di-O-benzyl-L-threitol
Mash EA, et al.
Organic Syntheses, 68, 92-92 (1990)
Chemistry Letters (Jpn), 2409-2409 (1987)
Chemistry Letters (Jpn), 1967-1967 (1986)

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