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Documentos Principais

T7642

Sigma-Aldrich

L-(+)-Threose

≥60%, syrup

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About This Item

Fórmula empírica (Notação de Hill):
C4H8O4
Número CAS:
Peso molecular:
120.10
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.25

Formulário

syrup

atividade óptica

[α]20/D 11.0 to 17.0, 48 hr, c = 2% (w/v) in water

concentração

≥60%

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

O[C@@H]1COC(O)[C@H]1O

InChI

1S/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2-,3+,4?/m1/s1

chave InChI

FMAORJIQYMIRHF-BCDHYOAOSA-N

Outras notas

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves


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Gertjan J M den Hartog et al.
Nutrition (Burbank, Los Angeles County, Calif.), 26(4), 449-458 (2009-07-28)
Hyperglycemia, oxidative stress, and the onset and progression of diabetic complications are strongly linked. Reduction of oxidative stress could be of utmost importance in the long-term treatment of diabetic patients. The chronic nature of the disease calls for a mode
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Chemical communications (Cambridge, England), 46(26), 4776-4778 (2010-05-21)
Esters of proteinogenic amino acids efficiently catalyse the formation of erythrose and threose under aqueous conditions in the highest yields and enantioselectivities yet reported. Remarkably while esters of (L)-proline yield (L)-carbohydrates, esters of (L)-leucine and (L)-alanine generate (D)-carbohydrates, offering the
Marc-Olivier Ebert et al.
Journal of the American Chemical Society, 130(45), 15105-15115 (2008-10-22)
TNA (alpha-( l)-threofuranosyl-(3'-2') nucleic acid) is a nucleic acid in which the ribofuranose building block of the natural nucleic acid RNA is replaced by the tetrofuranose alpha-( l)-threose. This shortens the repetitive unit of the backbone by one bond as
Masahide Sasaki et al.
Carbohydrate research, 343(5), 848-854 (2008-02-27)
An aqueous solution of glucose was reacted at temperatures from 200 to 400 degrees C under atmospheric pressure using a continuous flow reactor. For reaction temperatures above 300 degrees C, the liquid product yield was not sensitive to the temperature
Thorsten Allscher et al.
Carbohydrate research, 342(11), 1419-1426 (2007-05-29)
In this work, we present novel complexes of hydroxyaldehydes and ketones with palladium(II). The compounds are studied by two-dimensional NMR spectroscopy in solution (COSY, HMQC, HMBC). Glycolaldehyde, d-glyceraldehyde, glyoxal and 2,4-O-ethylidene-d-erythrose were used as aldehydes, d-erythrulose was used as an

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