Product Detail
Butanedinitrile-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.
Butanedinitrile-13C2 Product Information
Butanedinitrile-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-103840.
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
Butanedinitrile-13C2
CAS No.
79341-57-4
CAT No.
CS-T-103840
Molecular Formula
C₂¹³C₂H₄N₂
Molecular Weight
82.07
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
N#[13C]CC[13C]#N
IUPAC Name
Butanedinitrile-1,4-13C2
Hazard Compound
Refer MSDS for complete information.
Description
Overview
Butanedinitrile-13C2 is an intermediate in the synthesis of 1,4-Diaminobutane-1,4-13C2 Dihydrochloride (D416029), an isotope labelled compound of 1,4-Diaminobutane (D416025). 1,4-Diaminobutane is an amino acid degradation product. Used in the preparation of hexahydropyrimidines as novel hepatitis C virus inhibitors. Also a reagent in the synthesis of antibacterial castor oil-based polyurethane membranes.
Synonyms
Butanedinitrile-1,4-13C2; Succinonitrile-1,4-13C2
Application Notes
Butanedinitrile-13C2 is an intermediate in the synthesis of 1,4-Diaminobutane-1,4-13C2 Dihydrochloride (D416029), an isotope labelled compound of 1,4-Diaminobutane (D416025). 1,4-Diaminobutane is an amino acid degradation product. Used in the preparation of hexahydropyrimidines as novel hepatitis C virus inhibitors. Also a reagent in the synthesis of antibacterial castor oil-based polyurethane membranes.
References
Hwang, J. et al.: Eur. J. Med. Chem., 70, 315 (2013); Yari, A. et al.: J. Biomed. Mat. Res., 102A, 84 (2014);
