Product Detail
Dimethyl Carbonate-13C2
Stable Isotope Reagent
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotope Reagent
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Dimethyl Carbonate-13C2 Product Information
Dimethyl Carbonate-13C2 is listed under Stable Isotope Reagent. It is associated with - and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-103905.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
Dimethyl Carbonate-13C2
CAS No.
616-38-6(unlabelled)
CAT No.
CS-T-103905
Molecular Formula
C¹³C₂H₆O₃
Molecular Weight
92.06
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
O=C(O[13CH3])O[13CH3]
IUPAC Name
Methyl Carbonate-13C2; Carbonic-13C Acid; Di(methyl-13C) Ester
Hazard Compound
Refer MSDS for complete information.
Description
Overview
Dimethyl Carbonate-13C2 is an intermediate in the synthesis of Mecobalamin-13C (M202803) which is labeled Mecobalamin (M202803) which is one of the biologically active forms of vitamin B12; differing only by the substitution of a methyl for the cyano group. Coenzyme required in the biosynthesis of methionine. Vitamin (hematopoietic).
Synonyms
Methyl Carbonate-13C2; Carbonic-13C Acid; Di(methyl-13C) Ester
Application Notes
Dimethyl Carbonate-13C2 is an intermediate in the synthesis of Mecobalamin-13C (M202803) which is labeled Mecobalamin (M202803) which is one of the biologically active forms of vitamin B12; differing only by the substitution of a methyl for the cyano group. Coenzyme required in the biosynthesis of methionine. Vitamin (hematopoietic).
References
Kisliuk, R.L., Biochem. J., 75, 467 (1960), Guest, J.R., et al.: Nature, 195, 340 (1962), Dolphin, D., et al.: Methods Enzymol., 18, 34 (1971), Beck, W.S., et al.: Am. J. Hematol., 34, 83 (1990),
