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1,6-dichlorosucrose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61854-83-9

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61854-83-9 Usage

Origin

Derived from sucrose (table sugar)

Usage

Artificial sweetener in diet sodas, chewing gum, and sugar-free desserts

Sweetness

Approximately 600 times sweeter than sucrose

Caloric Content

Contains no calories

Popularity

Favored for sugar reduction and calorie control

Production

Selective chlorination of sucrose molecules

Body Recognition

Not recognized as a carbohydrate by the body

Metabolism

Not metabolized by the body

Safety

Studies show it is safe for consumption

Blood Sugar Impact

No adverse effects on blood sugar levels

Check Digit Verification of cas no

The CAS Registry Mumber 61854-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,5 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61854-83:
(7*6)+(6*1)+(5*8)+(4*5)+(3*4)+(2*8)+(1*3)=139
139 % 10 = 9
So 61854-83-9 is a valid CAS Registry Number.

61854-83-9SDS

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 1,6-dichloro-1,6-dideoxy-β-D-fructofuranosyl α-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names (2R,3R,4S,5S,6R)-2-((2R,3S,4S,5S)-2,5-Bis-chloromethyl-3,4-dihydroxy-tetrahydro-furan-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol

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:61854-83-9 SDS

61854-83-9Downstream Products

61854-83-9Relevant academic research and scientific papers

Synthesis of 1',6'-disubstituted sucroses and their behavior as glucosyl donors for a microbial α-glucosyltransferase

Kakinuma,Yuasa,Hashimoto

, p. 61 - 72 (1996)

Versatile 6'-chloro-6'-deoxy-1'-substituted sucrose derivatives were synthesized in search of an optimum donor substrate for the intermolecular transglucosylation with the α-glucosyltransferase from Protaminobacter rubrum. Two substituents at the C-1' and C-6' positions of sucrose were introduced utilizing the distinct reactivity of the corresponding sulfonates. Methyl β-D-arabinofuranoside was most efficiently glucosylated with the 1'-deoxy derivative 5. Hydroxyl and fluoro groups at C-1' show a tendency to enhance the intramolecular transglucosylations, giving 3-O-(α-D-glucopyranosyl)-D-fructose derivatives.

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