网站主页>>>项目整合精选>>>项目整合精选>>>Meparfynol CAS Registry Number: 77-75-8 甲戊炔醇

Meparfynol CAS Registry Number: 77-75-8 甲戊炔醇

CAS Name: 3-Methyl-1-pentyn-3-ol
Additional Names: ethyl ethynyl methyl carbinol; 2-ethynyl-2-butanol; methylparafynol; methylpentynol
Trademarks: Allotropal (Heyl); Anti-Stress (Sintyal); Apridol; Atemorin; Atempol (Norgine); Dalgol; Dorison; Dormalest; Dormidin; Dormigen; Dormiphen; Dormison (Schering); Dormosan; Formison; Hesofen; Hexofen; Imnudorm; Oblivon; Pentadorm; Perlopal; Riposon; Seral; Somnesin (Central Pharm.)
Percent Composition: C 73.43%, H 10.27%, O 16.30%

📌 参考资料/链接：
Literature References: Prepd from methyl ethyl ketone and sodium acetylide in liquid ammonia or by a Grignard reaction: DE 285770 (1913 to Bayer); also DE 289800 and DE 291185 see Frdl. 12, 55, 56, 57; Sung Wouseng, Ann. Chim. [10] 1, 343 (1924); Rupe, Vonaesch, Ann. 442, 80 (1925); Carothers, Coffman, J. Am. Chem. Soc. 54, 4071 (1932); Campbell et al., ibid. 60, 2882 (1938); Campbell, Campbell, Proc. Indiana Acad. Sci. 50, 123-127 (1940), C.A. 35, 5471; Smith, US 2385547 (1945 to Commercial Solvents); A. W. Johnson, The Chemistry of the Acetylenic Compounds vol. I (Edward Arnold Co., London, 1946) p 278; Hurd, McPhee, J. Am. Chem. Soc. 69, 239 (1947); P. Piganiol, Acetylene Homologs and Derivatives (Brooklyn, 1950); Papa et al., Arch. Biochem. Biophys. 33, 482 (1951); Thiele, Martinez, Ciencia (Mexico City) 15, 70 (1955). An optically active form has been described by Hickmann, Kenyon, J. Chem. Soc. 1955, 2051. Toxicity data: Margolin et al., Science 114, 384 (1951).

📄 详细内容

Properties: Mobile liquid. Acrid odor, burning taste. d420 0.8688. d2020 0.8721; 7.28 lbs/U.S. gal. bp760 121-122°; bp37 50°; bp6.5 20°. mp -30.6°. nD20 1.4318. Flash pt 101.3°F. Surface tension at 25°: 23.8 dynes/cm; 5% aq soln: 34.1 dynes/cm. Soly in water at 25°: 12.8 g/100 ml. Sol in ether. Miscible with acetone, benzene, carbon tetrachloride, Cellosolve, cyclohexanone, diethylene glycol, ethyl acetate, kerosene, methyl ethyl ketone, mineral spirits, ethanolamine, neatsfoot oil, petr ether, soybean oil, Stoddard solvent. LD50 orally in mice, rats, guinea pigs: 600-900 mg/kg (Margolin).
Melting point: mp -30.6°
Boiling point: bp760 121-122°; bp37 50°; bp6.5 20°
Flash point: Flash pt 101.3°F
Index of refraction: nD20 1.4318
Density: d420 0.8688; d2020 0.8721; 7.28 lbs/U.S. gal
Toxicity data: LD50 orally in mice, rats, guinea pigs: 600-900 mg/kg (Margolin)
Derivative Type: Carbamate
CAS Registry Number: 302-66-9
Trademarks: N-Oblivon; Oblivon C; Trusono
Percent Composition: C 59.56%, H 7.85%, N 9.92%, O 22.67%
Literature References: Prepn: McLamore et al., J. Org. Chem.
20, 1379 (1955); from 3-methyl-1-pentyn-3-ol, trichloroacetic acid, KOCN: McCrea et al.,
GB
761817 (1956 to British Schering). Acute toxicity: Soehring et al., Arzneim.-Forsch.
5, 161 (1955).
Properties: Crystals from ether + petr ether. mp 55.8-57° (McLamore); from cyclohexane, mp 53.5-55° (McCrea). bp16 120-121°; bp0.01 95°. Solubility in water: 1.6 g/100 ml. LD50 (4 hr) s.c. in mice: 0.56 g/kg (Soehring).
Melting point: mp 55.8-57° (McLamore); mp 53.5-55° (McCrea)
Boiling point: bp16 120-121°; bp0.01 95°
Toxicity data: LD50 (4 hr) s.c. in mice: 0.56 g/kg (Soehring)
Therap-Cat: Hypnotic; sedative.
Keywords: Sedative/Hypnotic; Alcohols.
产品链接: 77-75-8››

← 返回产品列表