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3343-70-2

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3343-70-2 Usage

General Description

D-[1-18O]GLUCOSE is a modified form of glucose in which the oxygen atom at position 1 is replaced with an isotope of oxygen, specifically oxygen-18. This isotopic substitution allows for the tracking and measurement of the metabolic fate of glucose in biological systems using spectroscopic and mass spectrometric techniques. It is commonly used in metabolic studies to investigate glucose uptake, utilization, and metabolic pathways in various physiological and pathological conditions, such as diabetes, cancer, and obesity. D-[1-18O]GLUCOSE is a valuable tool for understanding the role of glucose in metabolism and for elucidating the mechanisms underlying metabolic diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 3343-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3343-70:
(6*3)+(5*3)+(4*4)+(3*3)+(2*7)+(1*0)=72
72 % 10 = 2
So 3343-70-2 is a valid CAS Registry Number.

3343-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name D-[1-18O]GLUCOSE

1.2 Other means of identification

Product number -
Other names -

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:3343-70-2 SDS

3343-70-2Upstream product

3343-70-2Downstream Products

3343-70-2Relevant articles and documents

General methods for enriching aldoses with oxygen isotopes.

Clark Jr.,Barker

, p. 253 - 261 (1986)

Synthetic methods are described for enriching 4-, 5-, and 6-carbon aldoses with oxygen isotopes. The general approach includes exchange between H2(1)8O and the aldehyde group of an aldose, exchange of O-1 onto C-2 of both of the 2-epimeric aldoses formed by molybdate-resin epimerization, and chain extension using cyanide addition. These methods make possible the production of all 16 aldohexoses enriched at 5 of the 6 oxygen atoms, all 8 aldopentoses enriched at 4 of the 5 oxygen atoms, and the four aldotetroses enriched at 2 of the 4 oxygen atoms. The general applicability of these methods is illustrated by the synthesis of a group of 22 different, 18O-enriched, biologically important D-aldoses having 4, 5, and 6 carbon atoms. The group includes D-[1-, 2-, 3-, 4-, O]glucose, D-[1-, 2-, 3-, 4-, and 6-18O]mannose, D-[1-, 2-, 3-, and 5-18O]arabinose, D-[1- abd 2- 18O] erythorose, and D-[1- and 2-18O]threose. The g.l.c.-m.s. characterization of these sugars with respect to the position and degree of 18O-enrichment is reported. The potential of the methods for producing aldoses having oxygen labels at multiple positions, or aldoses labeled simultaneously with oxygen, hydrogen, and carbon isotopes is discussed.

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