Skip to Content
Merck
All Photos(1)

Documents

131695

Sigma-Aldrich

Pyrimidine

≥98.0%

Synonym(s):

1,3-Diazine, Metadiazine, m-Diazine

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

About This Item

Empirical Formula (Hill Notation):
C4H4N2
CAS Number:
289-95-2
Molecular Weight:
80.09
Beilstein:
103894
EC Number:
206-026-0
MDL number:
MFCD00006059
UNSPSC Code:
12352100
eCl@ss:
39161701
PubChem Substance ID:
24848029
NACRES:
NA.22

Assay

≥98.0%

refractive index

n20/D 1.504 (lit.)

bp

123-124 °C (lit.)

mp

19-22 °C (lit.)

solubility

H2O: soluble
alcohols: soluble
diethyl ether: soluble

density

1.016 g/mL at 25 °C (lit.)

SMILES string

c1cncnc1

InChI

1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H

InChI key

CZPWVGJYEJSRLH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Pyrimidine is a heterocyclic compound with excellent stability. It is used in manufacture of pharmaceuticals, agrochemicals and dyes.

Application

Pyrimidine was used to assess the extent of pyrimidine/purine asymmetry quantitatively. It was also used to study the photoinduced ion chemistry of the halogenated pyrimidines, a class of prototype radiosensitizing molecules.

accessory

Product No.
Description
Pricing

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H318

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

93.2 °F - closed cup

Flash Point(C)

34 °C - closed cup

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

Pyrimidine: a review on anticancer activity with key emphasis on SAR
Aastha M et al.
Future Journal of Pharmaceutical Sciences, 7, 123-123 (2021)
Y Vladimir Pabon-Martinez et al.
Scientific reports, 7(1), 11043-11043 (2017-09-10)
The anti-gene strategy is based on sequence-specific recognition of double-strand DNA by triplex forming (TFOs) or DNA strand invading oligonucleotides to modulate gene expression. To be efficient, the oligonucleotides (ONs) should target DNA selectively, with high affinity. Here we combined
Mattea Carmen Castrovilli et al.
Journal of the American Society for Mass Spectrometry, 25(3), 351-367 (2014-01-05)
In the present work, we studied the photoinduced ion chemistry of the halogenated pyrimidines, a class of prototype radiosensitizing molecules, in the energy region 9-15 eV. The work was stimulated by previous studies on inner shell site-selective fragmentation of the
Elke J A Hilgers et al.
Frontiers in plant science, 9, 1331-1331 (2018-10-20)
The xylulose 5-phosphate/phosphate translocator (XPT) represents the fourth functional member of the phosphate translocator (PT) family residing in the plastid inner envelope membrane. In contrast to the other three members, little is known on the physiological role of the XPT.
R Piechocki et al.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 49(6), 265-271 (1977-11-01)
The correlation between the evolutionary rates of proteins and frequencies of DNA-bases in the first and in the second position of corresponding codons was investigated.Adenine in the first and guanine in the second position showed the strongest positive correlation with
View All Related Papers

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