Basic information Description Heterocyclic compound Synthesis and Structure Safety Related Supplier
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Pyridazine

Basic information Description Heterocyclic compound Synthesis and Structure Safety Related Supplier
Pyridazine Basic information
Pyridazine Chemical Properties
  • Melting point:-8 °C (lit.)
  • Boiling point:208 °C (lit.)
  • Density 1.103 g/mL at 25 °C (lit.)
  • refractive index n20/D 1.524(lit.)
  • Flash point:185 °F
  • storage temp. Inert atmosphere,Room Temperature
  • form Liquid
  • pka2.24(at 20℃)
  • color Clear yellow-brown
  • Water Solubility MISCIBLE
  • Merck 14,7969
  • BRN 103906
  • InChIKeyPBMFSQRYOILNGV-UHFFFAOYSA-N
  • CAS DataBase Reference289-80-5(CAS DataBase Reference)
  • NIST Chemistry ReferencePyridazine(289-80-5)
  • EPA Substance Registry SystemPyridazine (289-80-5)
Safety Information
  • Hazard Codes Xn
  • Risk Statements 36/37/38-22
  • Safety Statements 23-24/25
  • RIDADR NA 1993 / PGIII
  • WGK Germany 3
  • RTECS UR5267000
  • 8-10
  • TSCA Yes
  • HS Code 29339980
  • ToxicityLD50 ipr-mus: 2650 mg/kg PBPHAW 1,542,65
MSDS
Pyridazine Usage And Synthesis
  • DescriptionPyridazine, sometimes called 1,2-diazine, is a six-membered ring containing two adjacent nitrogen atoms. Pyridazine is a privileged structure in medicinal chemistry and can be used as an isosteric replacement of phenyl or heteroaromatic rings. Pyridazines can improve the physiochemical properties of drug molecules by increasing their water solubility, participating as hydrogen bond acceptors, and have a high capacity to complex with targets due to their dipole moment. Pyridazine confers bioavailability, especially to the CNS, and can reduce toxicity. Pyridazine is a part of several drug molecules, and the pyradzine pharmacophore has led to a variety of pharmacologically active compounds.
  • Heterocyclic compoundPyridazine refers to a heterocyclic azine compound containing a nitrogen hexaheterocyclic , it and pyrimidine, pyrazine are isomers of each other , it is insoluble in petroleum ether, soluble in methanol, ethanol and ether, and it can be miscible with water, benzene and dimethyl formamide immiscibility. Pyridazine is a weak base, which can form salts with picric acid, and hydrochloric acid; pyridazine is not prone to nucleophilic and electrophilic aromatic substitution reaction; it is stable to potassium permanganate; sodium or alcohols may be reduced open-chain , and converted to 1,4-diaminobutane. Pyridazine is widely used as pharmaceutical raw materials, such as long-term sulfa SMP which is pyridazine derivative, 4-amino-cinnoline which belongs to antimalarials, blood pressure drug hydralazine, etc. all use pyridazine as raw materials; it can also be used as raw material of pesticides, for the production of herbicides, "herbicide-sensitive", "Milstem", "bromine herbicide-sensitive", "Kusakira," "maleic hydrazide", "Norflurazon", "pyridate "" insecticide "," imputed phosphorus "and so on.
  • Synthesis and StructurePyridazines are heterocyclic compounds with an N-N bond in their ring structure. The pyridazine molecule is a π-deficient heteroaromatic compound similar to pyridine. Due to the presence of the π-deficient nitrogen aromatic heterocycles these compounds are more easily soluble in water when compared to other hydrocarbons. The basic aromatic ring system of pyridazine contains two adjacent nitrogen atoms.
    The parent heterocycle was first prepared by oxidation of benzocinnoline to the pyridazinetetracarboxylic acid followed by decarboxylation. A better route to this otherwise esoteric compound starts with the maleic hydrazide. These heterocycles are often prepared via condensation of 1,4-diketones or 4-ketoacids with hydrazines.
    Pyridazines are effective water oxidation catalysts with high efficiency turnover numbers up to 700.
  • Chemical PropertiesClear yellowish-brown liquid
  • Safety ProfileModerately toxic by intraperitoneal route. When heated to decomposition it emits toxic vapors of NOx.
Pyridazine Preparation Products And Raw materials
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