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Merck

131695

Pyrimidine

≥98.0%

Synonym(s):

1,3-Diazine, Metadiazine, m-Diazine

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About This Item

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

Product Name

Pyrimidine, ≥98.0%

InChI key

CZPWVGJYEJSRLH-UHFFFAOYSA-N

InChI

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

SMILES string

c1cncnc1

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.)

Quality Level

100

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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.

General description

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

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H318

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

93.2 °F - closed cup

flash_point_c

34 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ1781
MKCX4066
MKCV3384
MKCT1973
MKCR6436

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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
Pyrimidine: a review on anticancer activity with key emphasis on SAR
Aastha M et al.
Future Journal of Pharmaceutical Sciences, 7, 123-123 (2021)
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)
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