18304-13-7

Basic information

• Product Name: CYANOETHYL SUCROSE
• Synonyms: CYANOETHYL SUCROSE;3,4,6-tetrakis-o-(2-cyanoethyl)-osyl;alpha-d-glucopyranoside,1,3,4,6-tetrakis-o-(2-cyanoethyl)-beta-d-fructofuran;octakis-O-(2-cyanoethyl)sucrose;Octa-(O-cyanoethyl)sucrose;α-D-Glucopyranoside, 1,3,4,6-tetrakis-O-(2-cyanoethyl) --D-fructofuranosyl 2,3,4,6-tetrakis-O-(2-cyanoethyl)-;1-O,3-O,4-O,6-O-Tetrakis(2-cyanoethyl)-β-D-fructofuranosyl 2-O,3-O,4-O,6-O-tetrakis(2-cyanoethyl)-α-D-glucopyranoside;2-O-[2-O,3-O,4-O,6-O-Tetrakis(2-cyanoethyl)-α-D-glucopyranosyl]-1-O,3-O,4-O,6-O-tetrakis(2-cyanoethyl)-β-D-fructofuranose
• CAS NO: 18304-13-7
• Molecular Formula: C₃₆H₄₆N₈O₁₁
• Molecular Weight: 766.8
• EINECS: 242-187-3
• Product Categories: Organics
• Mol File: 18304-13-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: -9.9°C
• Boiling Point: 735.34°C (rough estimate)
• Flash Point: 318.9 °C
• Appearance: Clear pale yellow to yellow/Viscous Liquid
• Density: 1.2
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.483-1.485
• CAS DataBase Reference: CYANOETHYL SUCROSE(CAS DataBase Reference)
• NIST Chemistry Reference: CYANOETHYL SUCROSE(18304-13-7)
• EPA Substance Registry System: CYANOETHYL SUCROSE(18304-13-7)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 18304-13-7(Hazardous Substances Data)

Usage

Chemical Properties

clear pale yellow to yellow viscous liquid

InChI:InChI=1/C36H46N8O11/c37-9-1-17-45-25-28-30(48-20-4-12-40)32(50-22-6-14-42)33(51-23-7-15-43)35(53-28)55-36(27-47-19-3-11-39)34(52-24-8-16-44)31(49-21-5-13-41)29(54-36)26-46-18-2-10-38/h28-35H,1-8,17-27H2/t28-,29-,30-,31-,32+,33-,34+,35-,36+/m1/s1

Upstream product

• 107-13-1 acrylonitrile 
• 57-50-1 Sucrose 

Relevant articles and documents

HYDROLYSIS OF CYANOETHYLATED CARBOHYDRATES: SYNTHESIS OF NEW CARBOXYLIC DERIVATIVES OF SUCROSE, D-GLUCOSE AND D-FRUCTOSE

Synthesis of new cyanoethylated compounds and carboxylic acids derived from sucrose, methyl D-glucopyranoside, methyl D-fructopyranoside annd methyl D-fructofuranoside are described.Basic hydrolysis of these cyanoethylated compounds to the corresponding amides and carboxylates and acidic hydrolysis to the corresponding methyl esters are discussed.