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Safety Information

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

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.

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

131695-250MG:
131695-BULK:
131695-VAR:
131695-5G:
131695-25G:
131695-1G:

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Certificates of Analysis (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)
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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
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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Global Trade Item Number

SKUGTIN
131695-250MG
131695-1G4061838728517
131695-25G4061838728524
131695-5G4061838117946

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