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D-Glyceraldehyde

CAS No.
453-17-8
Chemical Name:
D-Glyceraldehyde
Synonyms
D-Glycerose;D-Aldotriose;D-GLYCERALDEHYDE;Glyceraldehyde, D-;D-(+)-GLYCERALDEHYDE;D-Glyceraldehyde (>98.0% (HPLC), viscous;D-2,3-Dihydroxypropanal;(2R)-2,3-Dihydroxypropanal;(r)-2,3-dihydroxy-propanal
CBNumber:
CB4438195
Molecular Formula:
C3H6O3
Molecular Weight:
90.08
MDL Number:
MFCD00064378
MOL File:
453-17-8.mol
MSDS File:
SDS

D-Glyceraldehyde Properties

Melting point 127-129 C
alpha D25 +8.7° (c = 2 in H2O); D15 +21.2° (c = 18)
Boiling point bp17 127-129°; bp10 123-126°
Density 1.272±0.06 g/cm3(Predicted)
refractive index n20/D 1.494
Flash point 112 °C
storage temp. 2-8°C
solubility DMSO, Methanol (Slightly), Water (Slightly)
form liquid (viscous)
pka 12.60±0.20(Predicted)
color Clear Colourless to Light Brown
Merck 13,4494
BRN 1720474
CAS DataBase Reference 453-17-8(CAS DataBase Reference)
FDA UNII 41A680M0WB
NIST Chemistry Reference Propanal, 2,3-dihydroxy-, (r)-(453-17-8)

SAFETY

Risk and Safety Statements

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-27-36/37/39
WGK Germany  3
10-23

D-Glyceraldehyde price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 49800 D-(+)-Glyceraldehyde ≥98.0% (HPLC), viscous 453-17-8 1g $204 2022-05-15 Buy
Sigma-Aldrich 49800 D-(+)-Glyceraldehyde ≥98.0% (HPLC), viscous 453-17-8 5g $801 2022-05-15 Buy
Cayman Chemical 16493 D-(+)-Glyceraldehyde ≥95% 453-17-8 100mg $32 2022-04-27 Buy
Cayman Chemical 16493 D-(+)-Glyceraldehyde ≥95% 453-17-8 1g $173 2022-04-27 Buy
Cayman Chemical 16493 D-(+)-Glyceraldehyde ≥95% 453-17-8 500mg $102 2022-04-27 Buy
Product number Packaging Price Buy
49800 1g $204 Buy
49800 5g $801 Buy
16493 100mg $32 Buy
16493 1g $173 Buy
16493 500mg $102 Buy

D-Glyceraldehyde Chemical Properties,Uses,Production

Description

D-(+)-Glyceraldehyde is an intermediate in carbohydrate metabolism. It is phosphorylated by triose kinase to produce D-glyceraldehyde 3-phosphate, an intermediate in glycolysis, gluconeogenesis, photosynthesis, and other metabolic pathways.

Chemical Properties

CLEAR ORANGE SYRUP

Uses

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).

Uses

D-Glyceraldehyde is the simplest of all aldoses and have been shown to be the one of the carbonyl metabolite of dietary fructose.

Definition

ChEBI: The D-enantiomer of glyceraldehyde.

Purification Methods

enantiomer [453-17-8] is a syrup (70 + % H2O) with [] D +14o (c 2, H2O) and the dimethyl acetal has b 124-127 o/14mm and []15 +21o (c 18, H2O). [Beilstein 1 H 845, 1 IV 4114.]

96-26-4
453-17-8
Synthesis of D-Glyceraldehyde from 1,3-Dihydroxyacetone
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View Lastest Price from D-Glyceraldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
D-Glyceraldehyde pictures 2019-08-02 D-Glyceraldehyde
453-17-8
US $1.00 / KG 1KG 95-99% 500kg/month Career Henan Chemical Co

D-Glyceraldehyde Spectrum

D-(+)-GLYCERALDEHYDE D-GLYCERALDEHYDE Glyceraldehyde, D- D-GLYCERALDEHYDE, 80-90 WT. % SOLUTION I N WATER D-GLYCERALDEHYDE MINIMUM 70% D(+)GLYCERALDEHYDE extrapure (R)-(+)-Glyceraldehyde, D-Glyceraldehyde solution D(+)-Glyceraldehyde solution (2R)-2,3-Dihydroxypropanal D-2,3-Dihydroxypropanal D-2,3-Dihydroxypropionaldehyde D-Aldotriose D-Glycerose (2R)-2,3-Dihydroxypropionaldehyde D(+)-Glyceraldehyde, 80-90 wt% aqueous solution D-(+)-Glyceraldehyde >=98.0% (HPLC), viscous D-(+)-Glyceraldehyde, >=85% water solution Propanal,2,3-dihydroxy-, (2R)- D-(+)-Glyceraldehyde≥ 89% (HPLC) (r)-2,3-dihydroxy-propanal D-Glyceraldehyde (> 98.0% (HPLC), viscous 453-17-8 C3H6O3 Monosaccharides Specialty Synthesis Carbohydrate Synthesis Carbohydrate Synthesis Monosaccharides Specialty Synthesis chiral