GENTIOBIOSE CAS 554-91-6

Introduction:Basic information about GENTIOBIOSE CAS 554-91-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

GENTIOBIOSE Basic information

Product Name:GENTIOBIOSE
Synonyms:6-O-beta-D-Glucopyranosyl-D-glucose, Amygdalose;BETA-GENTOBIOSE;BETA-GENTIOBIOSE;BETA-D-GENTIOBIOSE;B-D-GENTIOBIOSE;GENTIOBIOSE;Gentiobiose, for biochemistry, 95%;D-Glucose, 6-O-.beta.-D-glucopyranosyl-
CAS:554-91-6
MF:C12H22O11
MW:342.3
EINECS:209-074-0
Product Categories:Basic Sugars (Mono & Oligosaccharides);Biochemistry;Disaccharides;Sugars;Dextrins、Sugar & Carbohydrates;Other APIs;carbohydrate
Mol File:554-91-6.mol

GENTIOBIOSE Chemical Properties

Melting point 195-197 °C (dec.)
Boiling point 397.76°C (rough estimate)
density 1.4149 (rough estimate)
refractive index 9.5 ° (C=4, H2O)
storage temp. Sealed in dry,2-8°C
solubility Water (Sparingly)
pka12.45±0.20(Predicted)
form Powder
color White to Off-white
Optical RotationAlpha type +21.4 → +8.7 Beta type -11 → +9.6
Water Solubility Slightly soluble in water.
Merck 14,4396
BRN 93354
Cosmetics Ingredients FunctionsSKIN CONDITIONING - HUMECTANT
InChIInChI=1/C12H22O11/c13-1-4(15)7(17)8(18)5(16)3-22-12-11(21)10(20)9(19)6(2-14)23-12/h1,4-12,14-21H,2-3H2/t4-,5+,6+,7+,8+,9+,10-,11+,12+/s3
InChIKeyAYRXSINWFIIFAE-XUYRYHIXNA-N
SMILES[C@H]1(OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)[C@H](O)[C@H]([C@H](O)[C@@H](CO)O1)O |&1:0,3,5,7,9,13,15,16,18,r|
CAS DataBase Reference554-91-6(CAS DataBase Reference)

Safety Information

WGK Germany 3
3-10
HS Code 29400090
Storage Class11 - Combustible Solids

GENTIOBIOSE Usage And Synthesis

Chemical Propertieswhite to off-white fine crystalline powder
UsesA disaccharide composed of two units of D-glucose
UsesGentiobiose was used in binding assays to determine if coelomic cytolytic factor 1 (CCF-1) binds to β-1,3-glucans to stimulate the pro-PO-activating system.
Purification Methods-Gentiobiose is best purified via the octaacetate which is recrystallised from MeOH, EtOH or better from methyl cellosolve by heating at 80o. The octaacetate (15g) is hydrolysed by suspending it in dry 0.05N NaOMe in MeOH (180mL) for 1hour with occasional shaking at room temperature. Dilute this with H2O to dissolve suspended matter, pass through Amberlite IR-120 and Duolite A-4 columns and the eluate is evaporated under reduced pressure to a syrup. Residual H2O is removed by repeated distillation with absolute EtOH under reduced pressure. The syrup is dissolved in methyl cellosolve (~40mL), filtered, nucleated and placed in an oven at 80o. The crystals are filtered off, washed with absolute EtOH (yield 6.7g, 89%), dried and have m 187-189o. Further recrystallisation from methyl cellosolve gives m 190o, and mutarotates from [] D 28 -1.5o (initial) to +10.6o (final, c 4, H2O). The -octaacetate has m 193o (crystallised from 95% EtOH) and has [] D 20 -5o (c 1.8, CHCl3). [Goldstein & Whelan Methods in Carbohydrate Chemistry I 313 1962, Academic Press, Beilstein 17/7 V 203.]

GENTIOBIOSE Preparation Products And Raw materials

Gentamicin sulfate CAS 1405-41-0
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