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N-DODECYL-BETA-D-GLUCOPYRANOSIDE

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Products Intro: Product Name:N-DODECYL-BETA-D-GLUCOPYRANOSIDE
CAS:59122-55-3
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Products Intro: Product Name:N-DODECYL-BETA-D-GLUCOPYRANOSIDE
CAS:59122-55-3
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CAS:59122-55-3
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Products Intro: Product Name:N-DODECYL-BETA-D-GLUCOPYRANOSIDE
CAS:59122-55-3
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N-DODECYL-BETA-D-GLUCOPYRANOSIDE manufacturers

N-DODECYL-BETA-D-GLUCOPYRANOSIDE Basic information
Product Name:N-DODECYL-BETA-D-GLUCOPYRANOSIDE
Synonyms:N-DODECYL GLUCOSIDE;N-DODECYL-BETA-D-GLC;N-DODECYL-BETA-D-GLUCOPYRANOSIDE;N-DODECYL B-D-GLUCOPYRANOSIDE;LAURYL MONOGLUCOSIDE;DODECYL-BETA-D-GLUCOPYRANOSIDE;DODECYLGLUCOPYRANOSIDE;DODECYL-GLUCOSIDE
CAS:59122-55-3
MF:C18H36O6
MW:348.48
EINECS:261-614-4
Product Categories:Glycon Biochem
Mol File:59122-55-3.mol
N-DODECYL-BETA-D-GLUCOPYRANOSIDE Structure
N-DODECYL-BETA-D-GLUCOPYRANOSIDE Chemical Properties
Melting point 77-137 °C
Boiling point 402.83°C (rough estimate)
density 1.0573 (rough estimate)
refractive index 1.4450 (estimate)
storage temp. −20°C
solubility Soluble in methanol at 50mg/ml
pka12.95±0.70(Predicted)
form Powder
color White to Off-white
BRN 86236
Stability:Stable. Incompatible with strong oxidizing agents.
InChIInChI=1/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18-/s3
InChIKeyPYIDGJJWBIBVIA-LQEOSLJMNA-N
SMILESO([C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CCCCCCCCCCCC |&1:1,2,3,5,7,r|
CAS DataBase Reference59122-55-3(CAS DataBase Reference)
EPA Substance Registry SystemDodecyl-beta-D-glucoside (59122-55-3)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-36/37/39-37/39
WGK Germany 3
3
HS Code 29389090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
N-DODECYL-BETA-D-GLUCOPYRANOSIDE Usage And Synthesis
Chemical Propertieswhite powder
Usesn-Dodecyl-beta-D-glucopyranoside is a non-ionic detergent.
Synthesis

A synthetic method of n-dodecyl-beta-D-glucopyranoside, comprising the steps of:

1) dissolving fully acetylated glucopyranoside, n-dodecyl alcohol and anhydrous tin tetrachloride in anhydrous dichloromethane, stirring the reaction for 20 minutes at room temperature, washing it with saturated aqueous potassium carbonate, collecting the organic phase, and distilling it under reduced pressure to obtain 1-n-dodecyl-2,3,4,6-tetraacetyl--D-glucopyranoside; the molar ratio of fully acetylated glucopyranoside, n-dodecyl alcohol and anhydrous tin tetrachloride was: 1:1.2:1.2; the ratio of fully acetylated glucopyranoside to anhydrous dichloromethane was 100g:550ml;

2) Dissolve 1-n-dodecyl-2,3,4,6-tetraacetyl--D-glucopyranoside in methanol, add sodium methoxide to adjust the pH to 9, and reacted at room temperature for 1.5 h. The reaction was adjusted to neutrality with a strongly acidic cation exchange resin Dowex-50, filtered, and the filtrate was evaporated out of the solvent, dried, and detected by NMR to give n-dodecyl-beta-D-glucopyranoside. 1-n-dodecyl-2,3,4,6-tetraacetyl--D-glucopyranoside to methanol ratio was 100 g:520 ml.

The yield was 57%. And the beta configuration was >97%.

N-DODECYL-BETA-D-GLUCOPYRANOSIDE Preparation Products And Raw materials
Tag:N-DODECYL-BETA-D-GLUCOPYRANOSIDE(59122-55-3) Related Product Information
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