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CAS No 86-54-4 , phthalazin-1-ylhydrazine

  • Name: phthalazin-1-ylhydrazine
  • Synonyms: Apresoline; Apresolin; Aprezolin;1-Hydrazinophthalazine; Apressin; Hydrazinophthalazine; Hydralazin; Hypophthalin;phthalazin-1-ylhydrazine;
  • CAS Registry Number:
  • Melting Point: 172 ºC
  • Safety Statements: Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Human systemic effects by ingestion: allergic dermatitis, cardiomyopathy, changes in coronary arteries. Human teratogenic effects by an unspecified route: developmental abnormalities of the blood and lymphatic system. Questionable carcinogen. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
  • EINECS: 201-680-3
  • Molecular Weight: 160.17592
  • InchiKey: RPTUSVTUFVMDQK-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H8N4/c9-11-8-7-4-2-1-3-6(7)5-10-12-8/h1-5H,9H2,(H,11,12)
  • Molecular Formula: C8H8N4
  • Molecular Structure:CAS No:86-54-4 phthalazin-1-ylhydrazine

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86-54-4 HYDRALAZINE,ENTERPRISE STANDARD

  • Hong kong Advanced Technology & Industrial Co., Ltd. [Manufacturer]
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86-54-4 hydralazine

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  • IUPAC NAME-1-hydrazinylphthalazine MOLECULAR FORMULA-C8H8N4 MOLAR MASS-160.176 g/mol ydralazine (apresoline) is a direct-acting smooth muscle relaxant used to treat hypertension by acting as a vasodilator primarily in arteries and arterioles. By rela...
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86-54-4 hydralazine

  • IUPAC NAME-1-hydrazinylphthalazine MOLECULAR FORMULA-C8H8N4 MOLAR MASS-160.176 g/mol Hydralazine is not used as a primary drug for treating hypertension because it elicits a reflex sympathetic stimulation of the heart (the baroreceptor reflex). The s...
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86-54-4 Hydralazine

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  • China VETCHEM Biochemistry Science [Manufacturer, Distributor/Wholesaler]
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References of phthalazin-1-ylhydrazine
Title: Hydralazine
CAS Registry Number: 86-54-4
CAS Name: 1(2H)-Phthalazinone hydrazone
Synonyms: 1-hydrazinophthalazine
Manufacturers' Codes: Ciba 5968; Pr?parat 5968; C-5968
Molecular Formula: C8H8N4
Molecular Weight: 160.18
Percent Composition: C 59.99%, H 5.03%, N 34.98%
Literature References: Prepd by the action of hydrazine hydrate on 1-chloro- or 1-phenoxyphthalazine: Hartmann, Druey, US 2484029 (1949 to Ciba); Druey, Ringier, Helv. Chim. Acta 34, 204 (1951). Metabolism: Z. H. Israile, P. G. Dayton, Drug Metab. Rev. 6, 283 (1977); K. Schmid et al., Arzneim.-Forsch. 31, 1143 (1981). Pharmacology: J. L. Cangiano et al., J. Lab. Clin. Med. 92, 516 (1978). Clinical paper: R. F. Albrecht et al., Int. Anesthesiol. Clin. 16, 299 (1978). Acute toxicity: L. Dorigotti et al., Pharmacol. Res. Commun. 8, 295 (1976). Comprehensive description: C. E. Orzech et al., Anal. Profiles Drug Subs. 8, 283-314 (1979).
Properties: Yellow needles from methanol, mp 172-173° (rapid heating). One gram dissolves in 3 ml 2N acetic acid, in 12 ml warm methanol. Forms a red compd (phthalazinylhydrazone) with acetone at 60° in presence of 2N acetic acid. LD50 in mice, rats (mg/kg): 122, 90 orally; 101, 40 i.p. (Dorigotti).
Melting point: mp 172-173° (rapid heating)
Toxicity data: LD50 in mice, rats (mg/kg): 122, 90 orally; 101, 40 i.p. (Dorigotti)
 
Derivative Type: Hydrochloride
CAS Registry Number: 304-20-1
Trademarks: Alphapress (Alphapharm); Apresoline (Novartis)
Molecular Formula: C8H8N4.HCl
Molecular Weight: 196.64
Percent Composition: C 48.86%, H 4.61%, N 28.49%, Cl 18.03%
Properties: Yellow crystals, dec 273°. Soly in water (g/100 ml) at 15°: 3.01; at 25°: 4.42; in 95% ethanol: 0.2 g/100 ml. Very slightly sol in ether. pH of a 2% aq soln 3.5 to 4.5. uv max (0.001% aq soln): 211, 240, 260, 304, 315 nm. Aq solns containing 20 mg/ml may be preserved with 0.5% chlorobutanol.
Absorption maximum: uv max (0.001% aq soln): 211, 240, 260, 304, 315 nm
 
Therap-Cat: Antihypertensive.
Keywords: Antihypertensive; Hydrazines/Phthalazines.