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131695

Sigma-Aldrich

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
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

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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’.

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Y Vladimir Pabon-Martinez et al.
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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)
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Polybrominated diphenyl ethers (PBDEs) as potential neurotoxicants in environment may possess hazards to human health. Previous studies have reported that PBDEs exposure could induce oxidative stress and disturb mitochondrial functions in mammalian cells. However, the toxicological mechanism remains to be
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ACS infectious diseases, 5(8), 1385-1396 (2019-05-24)
Marburg virus causes sporadic outbreaks of severe hemorrhagic fever with high case fatality rates. Approved, effective, and safe therapeutic or prophylactic countermeasures are lacking. To address this, we used phage display to engineer a synthetic antibody, sFab H3, which binds
Elke J A Hilgers et al.
Frontiers in plant science, 9, 1331-1331 (2018-10-20)
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