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Merck

251380

Sigma-Aldrich

L-(+)-Tartaric acid

ACS reagent, ≥99.5%

Sinónimos:

(2R,3R)-(+)-Tartaric acid, L-Threaric acid

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About This Item

Fórmula lineal:
HO2CCH(OH)CH(OH)CO2H
Número de CAS:
Peso molecular:
150.09
Beilstein/REAXYS Number:
1725147
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

agency

suitable for EPA 200.7
suitable for EPA 200.8

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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Dorothy N Nyangena et al.
Foods (Basel, Switzerland), 9(5) (2020-05-08)
Edible insects are increasingly being considered as food and feed ingredients because of their rich nutrient content. Already, edible insect farming has taken-off in Africa, but quality and safety concerns call for simple, actionable hazard control mechanisms. We examined the
(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)
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)
(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)
Chemistry Letters (Jpn), 1967-1967 (1986)

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This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

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