Skip to Content
MilliporeSigma
All Photos(1)

Documents

T8250

Sigma-Aldrich

D-Threonine

≥98% (TLC)

Synonym(s):

(2R,3S)-2-Amino-3-hydroxybutyric acid, D-α-Amino-β-hydroxybutyric acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H9NO3
CAS Number:
Molecular Weight:
119.12
Beilstein/REAXYS Number:
1721643
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:

Quality Level

assay

≥98% (TLC)

form

powder or crystals

technique(s)

UHPLC: suitable

color

white

mp

274 °C

solubility

H2O: soluble

SMILES string

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

InChI

1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m0/s1

InChI key

AYFVYJQAPQTCCC-STHAYSLISA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

D-Threonine is sweet and toxic in nature.It acts as an inhibitor of L-threonine dehydratase.

Application

D-Threonine has been used as a constituent of standard mix in Ultra-high performance liquid chromatography (UHPLC) system for quantification of amino acid racemization.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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

Customers Also Viewed

Slide 1 of 3

1 of 3

D-Valine ≥98%

Sigma-Aldrich

855987

D-Valine

D-Lysine ≥98% (HPLC)

Sigma-Aldrich

L8021

D-Lysine

DL-Serine ≥98% (TLC)

Sigma-Aldrich

S4375

DL-Serine

Kateryna Fesko et al.
Bioorganic & medicinal chemistry letters, 18(22), 5987-5990 (2008-09-02)
The Y265A mutant of alanine racemase (alrY265A) was evaluated as a catalyst for the synthesis of beta-hydroxy-alpha-amino acids. It promotes the PLP-dependent aldol condensation of glycine with a range of aromatic aldehydes. The desired products were obtained with complete stereocontrol
Alessandro Paiardini et al.
Biochimica et biophysica acta, 1647(1-2), 214-219 (2003-04-11)
Vitamin B(6)-dependent enzymes may be grouped into five evolutionarily unrelated families, each having a different fold. Within fold type I enzymes, L-threonine aldolase (L-TA) and fungal alanine racemase (AlaRac) belong to a subgroup of structurally and mechanistically closely related proteins
The Journal of Biological Chemistry, 244 (1969)
Fishmeal with different levels of biogenic amines in aquafeed: Comparison of feed protein quality, fish growth performance, and metabolism
Jasour M, et al.
Aquaculture (Amsterdam, Netherlands), 488, 80-89 (2018)
Test, 244 (1969)

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