Product Detail
Thymine-15N2,13C
Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotopes
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Thymine-15N2,13C Product Information
Thymine-15N2,13C is listed under Stable Isotopes. 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-99790.
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
Thymine-15N2,13C
CAS No.
-
CAT No.
CS-T-99790
Molecular Formula
C4¹³CH6¹5N2O2
Molecular Weight
129.09
Category
Storage Condition
Refer MSDS for complete information.
IUPAC Name
"Thymine-15N2,13C"
Hazard Compound
Refer MSDS for complete information.
Description
Overview
"Thymine-15N2,13C is a labelled analogue of Thymine (T412150), which is a nitrogenous base component in the nucleic acid of DNA. Thymine-15N2,13C is also an intermediate in synthesizing 5-Methyl Cytosine-13C,15N2 Hydrochloride (M294702), which is a labelled derivative of Dibarbituric acid."
Synonyms
"5-Methyl-2,4(1H,3H)-pyrimidinedione-15N2,13C; NSC 14705-15N2,13C; NSC 1686634-15N2,13C; 4-Hydroxy-5-methylyrimidin-2(1H)-one-15N2,13C; 5-Methyluracil-15N2,13C; USP Zidovudine Related Compound C-15N2,13C;"
Application Notes
"Thymine-15N2,13C is a labelled analogue of Thymine (T412150), which is a nitrogenous base component in the nucleic acid of DNA. Thymine-15N2,13C is also an intermediate in synthesizing 5-Methyl Cytosine-13C,15N2 Hydrochloride (M294702), which is a labelled derivative of Dibarbituric acid."
References
"Keum, Y., et al.: App. Microbiol. Biotechnol., 80, 863 (2008); Redzic, Z., et al.: Neurochem. Res., 34, 566 (2009); Lanevskij, K., et al.: J. Pharm. Sci., 98, 122 (2009); Rajendar, B., et al.: Bioorg. Med. Chem., 17, 351 (2009);"
