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水合肼

产品号 A14005 公司名称 Alfa Aesar
CAS号 7803-57-8 公司网站 http://www.alfa.com
分子式 H6N2O 电 话
分子量 50.06044 传 真
纯 度 98+% 电子邮件
保 存 Chembase数据库ID: 77861

产品价格信息

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产品别名

标题
Hydrazine monohydrate
IUPAC标准名
hydrazine hydrate
IUPAC传统名
hydrazine hydrate

产品登记号

默克索引号 144771
CAS号 7803-57-8
EC号 206-114-9
MDL号 MFCD00149931

产品性质

纯度 98+%
沸点 120-121°C
密度 1.027
闪点 75°C(167°F)
熔点 -52°C
折射率 1.4310
GHS危险品标识 GHS05
GHS危险品标识 GHS06
GHS危险品标识 GHS08
GHS危险品标识 GHS09
GHS危险声明 H301-H310-H330-H317-H350-H314-H318-H400-H410-H227
欧盟危险性物质标志 有毒(Toxic) 有毒(Toxic) (T)
欧盟危险性物质标志 环境危害性(Nature polluting) 环境危害性(Nature polluting) (N)
GHS警示性声明 P210-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P320-P330-P361-P405-P501A
危险公开号 45-23/24/25-34-43-50/53
RTECS编号 MV4590000
安全公开号 53-45-60-61
TSCA收录
联合国危险货物等级 8
联合国危险货物编号 UN2030
联合国危险货物包装类别(PG) II

产品详细信息

参考文献

  • Forms stable, water-free solid complexes consisting of one hydrazine molecule associated with one molecule of hydroquinone or two molecules of 4-methoxyphenol. These have potential as replacements for the very hazardous anhydrous hydrazine, e.g. in the solid state reaction with esters to give pure hydrazides: J. Chem. Soc., Chem. Commun., 1531, (1995).
  • Diimide precursor: for generation of diimide by oxidation with O2, and use in selective reduction of a double bond in the presence of a cyclopropane ring, see: J. Chem. Soc., Chem. Commun., 525 (1973). Review of diimide reductions: Org. React., 40, 91 (1991). See also Hydroxylamine-O-sulfonic acid, A12560.
  • In the Wolff-Kishner carbonyl to methylene reduction (heating with hydrazine and alkali hydroxide), diethylene glycol is now the usual solvent (the Huang Minlon modification): J. Am. Chem. Soc., 68, 2487 (1946); Org. Synth. Coll., 4, 510 (1963). The reduction has also been performed at ambient temperature by the use of KO-t-Bu in DMSO: J. Am. Chem. Soc., 84, 1734 (1962). See also Isatin, A12468 for an analogous reduction.
  • In the presence of Rh on carbon, nitrobenzene is selectively reduced to phenylhydroxylamine: Org. Synth. Coll., 8, 16 (1993).
  • For a brief feature on uses of the reagent in synthesis, see: Synlett, 2445 (2004).