Skip to Content
Merck
All Photos(1)

Key Documents

43456

Sigma-Aldrich

(+)-O,O′-Di-pivaloyl-D-tartaric acid

≥98.0%

Synonym(s):

(+)-DPTA

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
[(CH3)3CCO2CH(CO2H)-]2
CAS Number:
Molecular Weight:
318.32
Beilstein:
6894779
MDL number:
UNSPSC Code:
12352108
eCl@ss:
39021705
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98.0%

optical activity

[α]20/D +23.5±1°, c = 1.7% in dioxane

mp

127-130 °C (lit.)

SMILES string

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

InChI

1S/C14H22O8/c1-13(2,3)11(19)21-7(9(15)16)8(10(17)18)22-12(20)14(4,5)6/h7-8H,1-6H3,(H,15,16)(H,17,18)/t7-,8-/m0/s1

InChI key

UFHJEZDFEHUYCR-YUMQZZPRSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(+)-O,O′-Di-pivaloyl-D-tartaric acid is a chiral protonating agent (CPA).

Other Notes

Reagent for the "deracemization" of carbonyl compounds by enantio-selective protonation of enamines or Li-enolates ; Synthesis of optically active α-amino acids

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Enantioselective protonations: fundamental insights and new concepts.
Duhamel L, et al.
Tetrahedron Asymmetry, 15(23) (2004)
Deracemisation par protonation enantioselective.
L. Duhamel, J.-C. Plaquevent
Tetrahedron Letters, 2285-2285 (1977)
Deracemization by enantioselective protonation. A new method for the enantiomeric enrichment of. alpha.-amino acids.
L. Duhamel, J.-C. Plaquevent
Journal of the American Chemical Society, 100, 7415-7415 (1978)
L. Duhamel
Bulletin de la Societe Chimique De France, II, 421-421 (1984)
Ligand exchange in asymmetric reactions of lithium enolates: application to the deracemization of a-aminoacids.
L. Duhamel et al.
Tetrahedron Letters, 27, 4975-4975 (1986)

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