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131695

Sigma-Aldrich

Pyrimidine

≥98.0%

Sinónimos:

1,3-Diazine, Metadiazine, m-Diazine

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About This Item

Fórmula empírica (notación de Hill):
C4H4N2
Número de CAS:
289-95-2
Peso molecular:
80.09
Beilstein/REAXYS Number:
103894
EC Number:
206-026-0
MDL number:
MFCD00006059
UNSPSC Code:
12352100
eCl@ss:
39161701
PubChem Substance ID:
24848029
NACRES:
NA.22

Quality Level

100

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.

For use with

Referencia del producto
Descripción
Precios

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H318

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

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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Certificados de análisis (COA)

Lot/Batch Number
MKCN6931
MKCP1775
MKCP0144
MKCK4072
MKCD4441

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Zhi Tang et al.
Ecotoxicology and environmental safety, 182, 109427-109427 (2019-07-16)
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
Parmeshwar Amatya et al.
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
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
Sander Y A Rodenburg et al.
mBio, 10(4) (2019-07-11)
The oomycete pathogen Phytophthora infestans causes potato and tomato late blight, a disease that is a serious threat to agriculture. P. infestans is a hemibiotrophic pathogen, and during infection, it scavenges nutrients from living host cells for its own proliferation. To
Ana A Fernández-Ramos et al.
Scientific reports, 7(1), 10550-10550 (2017-09-07)
Metabolic reprogramming is critical for T cell fate and polarization and is regulated by metabolic checkpoints, including Myc, HIF-1α, AMPK and mTORC1. Our objective was to determine the impact of mycophenolic acid (MPA) in comparison with rapamycin (Rapa), an inhibitor
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