Skip to Content
Merck
CN

275514

6-Aza-2-thiothymine

99%

Synonym(s):

2-Thio-6-azathymine, 3,4-Dihydro-6-methyl-3-thioxo-1,2,4-triazin-5(2H)-one

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C4H5N3OS
CAS Number:
Molecular Weight:
143.17
EC Number:
210-445-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
4861
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

NKOPQOSBROLOFP-UHFFFAOYSA-N

InChI

1S/C4H5N3OS/c1-2-3(8)5-4(9)7-6-2/h1H3,(H2,5,7,8,9)

SMILES string

CC1=NNC(=S)NC1=O

assay

99%

mp

218-221 °C (lit.)

solubility

formic acid: soluble 5%, clear, colorless to light yellow-green

Application

6-Aza-2-thiothymine was used in the preparation of a matrix that was utilized for ionizing small molecules.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Selina Rahman Shanta et al.
The Analyst, 137(24), 5757-5762 (2012-10-23)
Since the development of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, this procedure has been specifically used for analyzing proteins or high molecular weight compounds because of the interference of matrix signals in the regions of the low mass range. Recently
Shi Yan et al.
Analytical chemistry, 90(1), 928-935 (2017-11-29)
Despite years of research, the glycome of the model nematode Caenorhabditis elegans is still not fully understood. Certainly, data over the years have indicated that this organism synthesizes unusual N-glycans with a range of galactose and fucose modifications on the
Rui-Rui Guo et al.
Frontiers in bioengineering and biotechnology, 8, 741-741 (2020-07-29)
Peptide-N4-(N-acetyl-β-glucosaminyl) asparagine amidases (PNGases, N-glycanases, EC 3.5.1.52) are indispensable tools in releasing N-glycans from glycoproteins. So far, only a limited number of PNGase candidates are available for the structural analysis of glycoproteins and their glycan moieties. Herein, a panel of
Alba Hykollari et al.
Electrophoresis, 38(17), 2175-2183 (2017-05-31)
The unusual nature of the N-glycans of the cellular slime mould Dictyostelium discoideum has been revealed by a number of studies, primarily based on examination of radiolabeled glycopeptides but more recently also by MS. The complexity of the N-glycomes of
David Weigt et al.
Scientific reports, 8(1), 11260-11260 (2018-07-28)
Recent advances in matrix-assisted laser desorption/ionization (MALDI) mass spectrometry have enabled whole cell-MALDI mass spectrometry biotyping of drug-treated cultured cells for rapid monitoring of known abundant pharmacodynamic protein markers such as polyacetylated histones. In contrast, generic and automated analytical workflows

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service