| Identification | More | [Name]
GENTIOBIOSE | [CAS]
554-91-6 | [Synonyms]
6-O-B-D-GLUCOPYRANOSYL-D-GLUCOSE
6-O-BETA-D-GLUCOPYRANOSYL-BETA-D-GLUCOSE
6-O-BETA-D-GLUCOPYRANOSYL-D-GLUCOSE
AMYGDALOSE
B-D-GENTIOBIOSE
BETA-D-GENTIOBIOSE
BETA-GENTIOBIOSE
BETA-GENTOBIOSE
GENTIOBIOSE
Gentiobiose, for biochemistry, 95%
D-Glucose, 6-O-.beta.-D-glucopyranosyl-
6-o-β-d-glucopyranosyl-d-glucose
6-O-β-D-Glucopyranosyl-D-glucose, Amygdalose
Gentiobiose, 95%, for biochemistry | [EINECS(EC#)]
209-074-0 | [Molecular Formula]
C12H22O11 | [MDL Number]
MFCD00198056 | [Molecular Weight]
342.3 | [MOL File]
554-91-6.mol |
| Chemical Properties | Back Directory | [Appearance]
white to off-white fine crystalline powder | [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. ]
0-6°C | [solubility ]
Water (Sparingly) | [form ]
Powder | [pka]
12.45±0.20(Predicted) | [color ]
White to Off-white | [Optical Rotation]
Alpha type +21.4 → +8.7 Beta type -11 → +9.6 | [Water Solubility ]
Slightly soluble in water. | [Merck ]
4396 | [BRN ]
93354 | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - HUMECTANT | [InChI]
InChI=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 | [InChIKey]
AYRXSINWFIIFAE-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 Reference]
554-91-6(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
white to off-white fine crystalline powder | [Uses]
A disaccharide composed of two units of D-glucose | [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.] |
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| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|