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.beta.-D-Galactopyranose

Product Name
.beta.-D-Galactopyranose
CAS No.
7296-64-2
Chemical Name
.beta.-D-Galactopyranose
Synonyms
β-D-Galactose;-β-D-Galactose;β-D-galactopyranose;.beta.-D-Galactopyranose;(2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol;(2R,3R,4S,5R,6R)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
CBNumber
CB31208989
Molecular Formula
C6H12O6
Formula Weight
180.16
MOL File
7296-64-2.mol
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.beta.-D-Galactopyranose Property

Melting point:
179-179.5 °C
Boiling point:
410.8±45.0 °C(Predicted)
Density 
1.732±0.06 g/cm3(Predicted)
storage temp. 
Hygroscopic, Refrigerator, under inert atmosphere
solubility 
Water (Slightly)
form 
Solid
pka
12.12±0.70(Predicted)
color 
White to Off-White
Stability:
Hygroscopic
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
G155265
Product name
β-D-Galactose
Packaging
50mg
Price
$1070
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CRB0002393
Product name
BETA-D-GALACTOPYRANOSE
Purity
95.00%
Packaging
5MG
Price
$500.31
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
58346
Product name
β-D-Galactose
Packaging
5mg
Price
$610
Updated
2021/12/16
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.beta.-D-Galactopyranose Chemical Properties,Usage,Production

Uses

β-D-Galactose s the beta anomer of D-Galactose (G155250), the C-4 epimer of Glucose (G595000). D-Galactose is found in milk and sugar beets as well as being synthesized by the body.

Definition

ChEBI: A D-galactopyranose having beta-configuration at the anomeric centre.

Purification Methods

D-Galactose (40g) is dissolved in hot H2O to establish the equilibrium of and anomers; then the solution is cooled to 0o and poured into absolute EtOH (500mL). Stir vigorously and crystallisation occurs within a few minutes, and more rapidly if seeded, filter the crystals immediately (7g, [] D 20 +65o (initial, c 4 in H2O). This mixture of and anomers is further separated by dissolving in an equal weight of cold H2O, filtering and adding to ice cold absolute EtOH (250mL) and stirring for 1minute when crystals separate, then filter them off. After two such crystallisations, the initial [] D 20 is +53o. This can be further purified by shaking with 80% EtOH for 2minutes, filtering, washing with EtOH and Et2O, and drying in a vacuum desiccator to give -Dgalactose (15g) with m 167o, [ ] D 20 +52o (initial, c 4 in H2O) mutarotating to +80.4o. Acetylation of Dgalactose with hot NaOAc/Ac2O gives -D-galactopyranoside pentaacetate m 1 4 2o, [ ] D 25 +25 (c 4 in CHCl3). [Wolfrom & Thompson Methods in Carbohydrate Chemistry I 120 1962, Academic Press, Beilstein 1 IV 4336.]

.beta.-D-Galactopyranose Preparation Products And Raw materials

Raw materials

Preparation Products

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.beta.-D-Galactopyranose Suppliers

J & K SCIENTIFIC LTD.
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7296-64-2, .beta.-D-GalactopyranoseRelated Search:


  • .beta.-D-Galactopyranose
  • (2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
  • β-D-Galactose
  • β-D-galactopyranose
  • -β-D-Galactose
  • (2R,3R,4S,5R,6R)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
  • 7296-64-2
  • Carbohydrates & Derivatives, Pharmaceuticals, Intermediates & Fine Chemicals