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49800

Sigma-Aldrich

D-(+)-Glyceraldehyde

≥98.0% (HPLC), viscous

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Synonym(s):
(2R)-2,3-Dihydroxypropanal, Triose
Empirical Formula (Hill Notation):
C3H6O3
CAS Number:
Molecular Weight:
90.08
Beilstein/REAXYS Number:
1720474
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98.0% (HPLC)

form

liquid (or viscous liquid)

impurities

≤10% water

storage temp.

2-8°C

SMILES string

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

InChI

1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m0/s1

InChI key

MNQZXJOMYWMBOU-VKHMYHEASA-N

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1 of 4

This Item
P50404G500173572
D-(+)-Glyceraldehyde ≥98.0% (HPLC), viscous

49800

D-(+)-Glyceraldehyde

1,3-Propanediol 98%

P50404

1,3-Propanediol

DL-Glyceraldehyde ≥90% (GC)

G5001

DL-Glyceraldehyde

L-(−)-Glyceraldehyde ≥90% (HPLC)

73572

L-(−)-Glyceraldehyde

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

form

liquid (or viscous liquid)

form

-

form

powder

form

liquid

storage temp.

2-8°C

storage temp.

-

storage temp.

room temp

storage temp.

2-8°C

impurities

≤10% water

impurities

-

impurities

-

impurities

-

Application

D-(+)-Glyceraldehyde can be utilized as a reactant in the synthesis of:
  • (S)-homophenylalanine by ruthenium oxidation of a 3-amino-1,2-diol generated via coupling of an amine, and α-hydroxyaldehyde.
  • β- and γ-allenols via metal-catalyzed cyclization. Allenols are used as a key precursor for the preparation of enantiopure dihydropyrans and tetrahydrooxepines.
  • Isopropylidene D-glyceraldehyde intermediate, which controls the chirality in the total synthesis of prostaglandins (PGE1).

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves


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