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sucralose-6-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105066-21-5 Structure
  • Basic information

    1. Product Name: sucralose-6-acetate
    2. Synonyms: sucralose-6-acetate
    3. CAS NO:105066-21-5
    4. Molecular Formula:
    5. Molecular Weight: 439.674
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105066-21-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: sucralose-6-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: sucralose-6-acetate(105066-21-5)
    11. EPA Substance Registry System: sucralose-6-acetate(105066-21-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 105066-21-5(Hazardous Substances Data)

105066-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105066-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,6 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105066-21:
(8*1)+(7*0)+(6*5)+(5*0)+(4*6)+(3*6)+(2*2)+(1*1)=85
85 % 10 = 5
So 105066-21-5 is a valid CAS Registry Number.

105066-21-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,1',6'-trichloro-4,1',6'-trideoxy-galactosucrose-6-acetate

1.2 Other means of identification

Product number -
Other names 6-acetyl-1',6'-dichloro-1',6'-dideoxy-β-fructofuranosyl-4-chloro-4-deoxy-galactopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105066-21-5 SDS

105066-21-5Upstream product

105066-21-5Relevant articles and documents

CHLORINATION OF SUCROSE-6-ESTERS

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Page/Page column 25; 26, (2015/07/07)

There is provided a method for the chlorination of a sucrose-6-acylate to produce a 4,1',6'-trichloro-4,1',6'-trideoxy-galactosucrose-6-acylate, wherein said method comprises the following steps (i) to (v): (i) providing a first component comprising sucrose-6-acylate; (ii) providing a second component comprising a chlorinating agent; (iii) combining said first component and said second component to afford a mixture; (iv) heating said mixture for a heating period in order to provide chlorination of sucrose- 6-acylate at the 4, 1' and 6' positions thereof; (v) quenching said mixture to produce a 4,1',6'-trichloro-4,1',6'-trideoxy- galactosucrose-6-acylate; wherein at least one of said first component and said second component comprises a reaction vehicle, and said reaction vehicle comprises a tertiary amide; and wherein said mixture comprises a cosolvent during a least a portion of the heating period of step (iv), wherein said cosolvent comprises perfluorooctane.

Novel Preparation of 6-O-Acyl Chlorosucrose from Anhydrous Cholorinated Reaction Mass

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Page/Page column 2, (2010/07/04)

A process is described for production of a chlorinated sucrose from a process stream containing a 6-O-protected chlorinated sucrose derived from chlorination of 6-O-protected sucrose wherein the process stream is treated under conditions which prevent or reverse deacylation of 6-O-protected chlorinated sucrose, extracting the same in a solvent, washing most of the dimethylformamide free from the solvent extract by repeated washing with saturated sodium chloride solution, isolating the 6-O-protected sucrose as a pure fraction and obtaining a chlorinated sucrose by deacylating the same.

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