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Fomepizola

Fomepizola
Struktur kimia bagi fomepizola
Nama
Nama IUPAC
4-metil-1H-pirazola
Nama lain
4-metilpirazola
Pengecam
Imej model 3D Jmol
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.028.587
KEGG
UNII
  • InChI=1S/C4H6N2/c1-4-2-5-6-3-4/h2-3H,1H3,(H,5,6) ☑Y
    Key: RIKMMFOAQPJVMX-UHFFFAOYSA-N ☑Y
  • InChI=1/C4H6N2/c1-4-2-5-6-3-4/h2-3H,1H3,(H,5,6)
    Key: RIKMMFOAQPJVMX-UHFFFAOYAT
  • n1cc(cn1)C
Sifat
C4H6N2
Jisim molar 82.11 g·mol−1
Ketumpatan 0.99 g/cm3
Takat didih 204-207 °C (97,3 kPa)
Bahaya
Takat kilat 96.0 °C (204.8 °F; 369.1 K)
Kecuali jika dinyatakan sebaliknya, data diberikan untuk bahan-bahan dalam keadaan piawainya (pada 25 °C [77 °F], 100 kPa).
 ☑Y pengesahan (apa yang perlu☑Y/N?)
Rujukan kotak info

Fomepizola atau 4-metilpirazola ditunjukkan untuk kegunaan sebagai antidot dalam keracunan metanol[1] atau etilena glikol[2] sah atau tersyak. Bahan ini boleh digunakan sendirian atau bergabung dengan hemodialisis. Selain kegunaan perubatan, peranan 4-metilpirazola dalam kimia koordinasi telah dikaji.[3]

  1. ^ International Programme on Chemical Safety (IPCS): Methanol (PIM 335), [1], dicapai pada 1 Mac 2008
  2. ^ Velez LI, Shepherd G, Lee YC, Keyes DC (September 2007). "Ethylene glycol ingestion treated only with fomepizole" (PDF). J Med Toxicol. 3 (3): 125–8. doi:10.1007/BF03160922. PMID 18072148.CS1 maint: multiple names: authors list (link)[pautan mati kekal]
  3. ^ Vos, Johannes G.; Groeneveld, Willem L. (1979). "Pyrazolato and related anions. Part V. Transition metal salts of 4-methylpyrazole". Transition Metal Chemistry. 4 (3): 137. doi:10.1007/BF00619054.

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Fomepizola
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