Product Detail
2-Butyne-1,4-diol-13C4
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.
2-Butyne-1,4-diol-13C4 Product Information
2-Butyne-1,4-diol-13C4 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-103853.
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
2-Butyne-1,4-diol-13C4
CAS No.
861954-06-5
CAT No.
CS-T-103853
Molecular Formula
¹³C₄H₆O₂
Molecular Weight
90.06
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
O[13CH2][13C]#[13C][13CH2]O
IUPAC Name
1,4-Dihydroxy-2-butynel-13C4
Hazard Compound
Refer MSDS for complete information.
Description
Overview
"2-Butyne-1,4-diol-13C4 is an intermediate in the synthesis of N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine-13C4 (A173713). N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine-13C4 is labelled N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine (A173710), which is a metabolite of butadiene.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package"
Synonyms
1,4-Dihydroxy-2-butynel-13C4
Application Notes
"2-Butyne-1,4-diol-13C4 is an intermediate in the synthesis of N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine-13C4 (A173713). N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine-13C4 is labelled N-Acetyl-S-(3,4-dihydroxybutyl)-L-cysteine (A173710), which is a metabolite of butadiene.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package"
References
Heavner, D., et al.: J. Pharm. Biomed. Anal., 40, 928 (2006); Carmella, S., et al.: Chem. Res. Toxicol., 22, 734 (2009)
