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Pyrimidine

Six-membered heterocyclic compounds Uses Pyrimidine base The functions of purine, pyrimidine and other substances Preparation Fluorouracil Chemical properties
Pyrimidine
Pyrimidine structure
CAS No.
289-95-2
Chemical Name:
Pyrimidine
Synonyms
iazine;Miazine;Pyrimidin;m-Diazine;1,3-Diazin;PYRIMIDINE;1,3-DIAZINE;Metadiazine;Pyrimidine,99%;Pyrimidine ,98%
CBNumber:
CB6224079
Molecular Formula:
C4H4N2
Formula Weight:
80.09
MOL File:
289-95-2.mol

Pyrimidine Properties

Melting point:
19-22 °C(lit.)
Boiling point:
123-124 °C(lit.)
Density 
1.016 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.504(lit.)
Flash point:
88 °F
storage temp. 
Flammables area
solubility 
soluble
form 
Liquid
pka
1.23(at 20℃)
color 
Clear colorless to orange
Water Solubility 
soluble
Sensitive 
Hygroscopic
Merck 
14,7987
BRN 
103894
Stability:
Stable, but air-sensitive and hygroscopic. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents, carbon dioxide. Flammable.
CAS DataBase Reference
289-95-2(CAS DataBase Reference)
NIST Chemistry Reference
1,3-Diazine(289-95-2)
EPA Substance Registry System
Pyrimidine(289-95-2)
SAFETY
  • Risk and Safety Statements
  • Hazard and Precautionary Statements (GHS)
Risk Statements  10
Safety Statements  23-24/25-16
RIDADR  UN 1993 3/PG 3
WGK Germany  3
RTECS  UV6263000
TSCA  Yes
HazardClass  3
PackingGroup  III
HS Code  29335990
Symbol(GHS):
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H226 Flammable liquid and vapour Flammable liquids Category 3 Warning
Precautionary statements:
P210 Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P240 Ground/bond container and receiving equipment.
P241 Use explosion-proof electrical/ventilating/lighting/…/equipment.
P303+P361+P353 IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

Pyrimidine price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 131695 Pyrimidine ≥98.0% 289-95-2 1g $31.4 2018-11-13 Buy
Sigma-Aldrich 131695 Pyrimidine ≥98.0% 289-95-2 5g $102 2018-11-13 Buy
TCI Chemical P0662 Pyrimidine free base >98.0%(GC)(T) 289-95-2 1g $24 2018-11-22 Buy
TCI Chemical P0662 Pyrimidine free base >98.0%(GC)(T) 289-95-2 5g $71 2018-11-22 Buy
Alfa Aesar A15534 Pyrimidine, 99% 289-95-2 5g $91.1 2018-11-13 Buy

Pyrimidine Chemical Properties,Uses,Production

Six-membered heterocyclic compounds

Pyridine, also known as "metadiazine", is a six-membered heteroaromatic ring compound containing two nitrogen atoms in the meta-position, being isomers with pyridazine and pyrazine. It has a molecular formula of C4H4N2 with the molecular weight being 80.09. It appears as colorless liquid or solid crystals with a pungent odor. It has a melting temperature of 20~22 ℃, boiling point of 123~124 °C and refractive index of 1.4998 (20 °C). It is easily soluble in water, ethanol and ether with weak alkaline and being capable of forming salts with acid. Its alkalinity is weaker than pyridine. It is also more difficult for it to participate into electrophilic substitution reaction than pyridine. It can only undergo bromination at the 5th position and is not capable of having nitrification and sulfonation reaction, but more prone to participate into nucleophilic substitution. Pyrimidine derivatives are widely found in nature. For example, vitamin B1, uracil, cytosine and thymine all contain pyrimidine structure. Its picrate salt appears as yellow needle-like crystals. It has a melting temperature of 156 °C. Owing to the presence of conjugated double bonds in the structure, pyrimidine has strong absorption capability on ultraviolet light. It is manufactured through phosphorus oxychloride oxidation of barbituric acid, followed by reduction through hydrogen iodide.
Nucleic acid contains three important pyrimidine derivatives, being an important base in nucleic acid, plays an important role in the body of organisms.
Nucleic acid contains three important pyrimidine derivatives, being an important base in nucleic acid, plays an important role in the body of organisms.
DNA mainly contains cytosine and thymine while RNA mainly contains cytosine and uracil, in some nucleic acids, there are also small amount of pyrimidine modified base, for example:
DNA mainly contains cytosine and thymine while RNA mainly contains cytosine and uracil, in some nucleic acids, there are also small amount of pyrimidine modified base
Sulfadiazine and its derivatives are commonly used antibacterial anti-inflammatory drugs.
The above information is edited by Andy Edwards of Chemicalbook.

Uses

1. It has no direct applications itself with its derivatives cytosine, uracil and thymine being important components of nucleic acid. Many drugs (such as sulfadiazine, trimethoprim and 6-mercaptopurine) contain pyrimidine ring.
2. Pyrimidine is widely used as pharmaceutical raw materials for the production of vitamin B, sulfadiazine, sulfadimidine, sulfamonomethoxine pyrimidine; pesticide raw materials, such as diazinon, pyrimidinol, blasticidin, bromacil, rumacil, crimidine, dodemorph, dimethirimol, ethirimol, bupirimate, pirazinon, pirimicarb, primicid, pirimiphos-methyl, polyoxin, pyramat, Pirimiphos-ethyl, etrimfos, triarimol, fenarimol and uracil, etc.; dye raw materials, for example, dyes with trihalogenated pyrimidine nucleus can react well with fiber and as reactive dyes, they have attracted people's attention.
3. It can be used as pharmaceutical intermediates, raw materials such as photosensitive agent

Pyrimidine base

Pyrimidine base is one of the chemical compositions of the nucleotides. It consists of carbon, nitrogen, hydrogen, oxygen and other elements. Pyrimidine bases include uracil, cytosine, and thymine, where uracil and cytosine constitute the bases in ribonucleic acid molecules while thymine and cytosine constitute bases in deoxyribonucleic acid molecules. Pyrimidine base has a strong absorption on ultraviolet in the wavelength of 250~280nm. The raw materials for its synthesis are derived from carbamoyl phosphate and aspartic acid. Pyrimidine base can also be metabolized into carbon dioxide, β-alanine and β amino-isobutyric acid and other substances. Some patients, due to congenital factors or taking certain drugs, can get pyrimidine alkali metabolic disorders, causing whey aciduria.

The functions of purine, pyrimidine and other substances

Purines and pyrimidines are essential heterocyclic nitrogen-containing compounds that used in nucleic acid metabolism in organisms (including humans) and are important substances in the formation of ribonucleic acid and deoxyribonucleic acid in cells. Purine, pyrimidine and ribose and phosphate can combine to form RNA; purine, pyrimidine and deoxyribose can bind to phosphate to produce DNA. DNA is the main chemical constituent of genes, which plays an important role in the transmission of genes (genetics); the main function of RNA is the regulation of intracellular protein synthesis. The final product of purine metabolism is mainly uric acid. Barley and malt contains 0.2% to 0.3% of the dry matter of nucleic acid. Upon the saccharification, the dry matter of nucleic acid can be subject to the degradation of various phosphatases to form nucleotides, nucleosides, purines and pyrimidine and many other degradation products, of which only purine and pyrimidine can enter into yeast cells to constitute ribonucleic acid, deoxyribonucleic acid, adenosine triphosphate and some coenzymes. Nucleotides are difficult to be absorbed. If the medium is lack of purine and pyrimidine, the cells have to rely on carbohydrates and amino acids for synthesis, thus consuming a lot of energy and influence the proliferation of yeast. In general, wort is not lack of the required purine and pyrimidine.
References: Chinese Medical Encyclopedia Editorial Board Editor; Guo Di editor in chief. Chinese Encyclopedia of Medicine • fifty-seven pediatrics.

Preparation

1, take malondialdehyde and formamide as raw materials and have reaction upon heating; we can obtain pyrimidine.
2, it can be manufactured through the catalytic hydrogenation of 2, 4-dichloropyrimidine in the system.
3, use zinc powder to reduce 2, 4, 6-trichloropyrimidine, pyrimidine can be obtained.
4, the reaction between ethyl acetoacetate and amidine (below) can produce pyrimidine.

Fluorouracil

Fluorouracil is a pyrimidine antimetabolite. In the body, it is first converted into 5-fluoro-2-deoxyuridine nucleotides (FUdRP), causing inhibition of thymidylate synthase (TMPS), preventing the conversion of deoxyuridine nucleotide into thymidine, interfering with DNA synthesis and leading to cell damage and death. It has a stronger effect in the presence of leucovorin (CF) because FUdRP, FH4 and TMPS can form triple complexes making the active metabolite of drug bind more tightly with the enzyme, so addition of CF when applying will yield better efficacy, especially improving the efficacy upon being applied to colorectal cancer. This product is cell cycle-specific drugs with killing effects on proliferated cells at all stages. It is most sensitive to the S phase, and also has retardation effect on the G1/S border. Oral absorption is not complete, and the drug is easily inactivated upon liver metabolism. After intravenous infusion or arterial infusion, the blood concentration is relatively stable.
Fluorouracil has relative significant effect against choriocarcinoma and malignant mole. It also has certain curative effects on gastric cancer, colon cancer, rectum cancer, liver cancer, pancreatic cancer, breast cancer, ovarian cancer, cervical cancer, prostate cancer, bladder cancer, kidney cancer, lung cancer, head and neck cancer and skin cancer.

Chemical properties

It appears as colorless crystalline or liquid.

Chemical Properties

Colourless to pale yellow liquid

Uses

Pyrimidine is used as building block in chemical synthesis. Product Data Sheet

Definition

One of a group of basic compounds found in living matter. They may be isolated fol- lowing complete hydrolysis of nucleic acids. They include uracil, thymine, cytosine, and methylcy- tosine. Thiamine is also a pyrimidine derivative. Other pyrimidines such

Definition

A simple nitrogenous organic molecule whose ring structure is contained in the pyrimidine bases cytosine, thymine, and uracil, which are constituents of the nucleic acids.

Definition

pyrimidine: An organic nitrogenousbase (see formula), sparinglysoluble in water, that gives rise to agroup of biologically important derivatives,notably uracil, thymine,and cytosine, which occur in nucleotidesand nucleic acids (DNA andRNA).

Pyrimidine Preparation Products And Raw materials

Raw materials

Preparation Products


Pyrimidine Suppliers

Global( 194)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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Henan DaKen Chemical CO.,LTD.
+86-371-55531817
info@dakenchem.com CHINA 21954 58
Henan Tianfu Chemical Co.,Ltd.
0371-55170693
0371-55170693 info@tianfuchem.com CHINA 20680 55
Mainchem Co., Ltd.
+86-0592-6210733
+86-0592-6210733 sales@mainchem.com CHINA 32457 55
Xiamen AmoyChem Co., Ltd
+86 (0)592-605 1114
sales@amoychem.com CHINA 6374 58
Chemwill Asia Co.,Ltd.
86-21-51086038
86-21-51861608 chemwill_asia@126.com;sales@chemwill.com;chemwill@hotmail.com;chemwill@gmail.com CHINA 24001 58
career henan chemical co
+86-371-86658258
sales@coreychem.com CHINA 20331 58
J & K SCIENTIFIC LTD. 400-666-7788 +86-10-82848833
+86-10-82849933 jkinfo@jkchemical.com;market6@jkchemical.com China 96519 76
Meryer (Shanghai) Chemical Technology Co., Ltd. +86-(0)21-61259100(Shanghai) +86-(0)755-86170099(ShenZhen) +86-(0)10-62670440(Beijing)
+86-(0)21-61259102(Shanghai) +86-(0)755-86170066(ShenZhen) +86-(0)10-88580358(Beijing) sh@meryer.com China 40277 62
Alfa Aesar 400-610-6006; 021-67582000
021-67582001/03/05 saleschina@alfa-asia.com China 30168 84

View Lastest Price from Pyrimidine manufacturers

Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
2018-12-24 Pyrimidine
289-95-2
US $1.00 / kg 1kg 98% as request career henan chemical co

Pyrimidine Spectrum


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