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.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
Molecular Weight:
180.16
MDL Number:
MOL File:
7296-64-2.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

.beta.-D-Galactopyranose Properties

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
FDA UNII RQ6K52J67A

.beta.-D-Galactopyranose price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC G155265 β-D-Galactose 7296-64-2 50mg $1070 2021-12-16 Buy
American Custom Chemicals Corporation CRB0002393 BETA-D-GALACTOPYRANOSE 95.00% 7296-64-2 5MG $500.31 2021-12-16 Buy
Medical Isotopes, Inc. 58346 β-D-Galactose 7296-64-2 5mg $610 2021-12-16 Buy
Product number Packaging Price Buy
G155265 50mg $1070 Buy
CRB0002393 5MG $500.31 Buy
58346 5mg $610 Buy

.beta.-D-Galactopyranose Chemical Properties,Uses,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.]

1580052-51-2
492-61-5
2460-44-8
6014-42-2
7296-64-2
7296-55-1
Synthesis of .beta.-D-Galactopyranose from Ethanamine, N-[(3,5-dichlorophenyl)methylene]-2,2-diethoxy-

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

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.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