Skip to Content
Merck
All Photos(1)

Documents

855049

Sigma-Aldrich

5-Azacytosine

Synonym(s):

2-Hydroxy-4-aminotriazine, 4-Amino-1,3,5-triazin-2-ol, 4-Amino-1,3,5-triazin-2-one, 4-Amino-2-hydroxy-1,3,5-triazine, NSC 51100, NSC 54006

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C3H4N4O
CAS Number:
931-86-2
Molecular Weight:
112.09
Beilstein:
116378
EC Number:
213-242-9
MDL number:
MFCD00006033
UNSPSC Code:
12352100
PubChem Substance ID:
24888369
NACRES:
NA.22

form

powder

mp

>300 °C (lit.)

SMILES string

NC1=NC(=O)NC=N1

InChI

1S/C3H4N4O/c4-2-5-1-6-3(8)7-2/h1H,(H3,4,5,6,7,8)

InChI key

MFEFTTYGMZOIKO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Reactant for:
  • Enzymic synthesis of nucleoside analogs using immobilized 2′-deoxyribosyltransferase from Lactobacillus reuteri
  • Reactions with oxide radical ion

  • Potential antitumor and antiproliferative agent against human leukemia cells

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

5-Aza-2′-deoxycytidine ≥97%

Sigma-Aldrich

A3656

5-Aza-2′-deoxycytidine

s-Triazine 97%

Sigma-Aldrich

T46051

s-Triazine

Mariana B Méndez et al.
AMB Express, 10(1), 173-173 (2020-09-30)
A novel IDA-LaNDT derivative was able to reach the highest productivity in the biosynthesis of a well-known antitumoral agent called decitabine. However, the combination of two simple and inexpensive techniques such as ionic absorption and gel entrapment with the incorporation

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