物质信息

ID:717708

名称和标识
别名
Hydroxylammonium chlorideHydroxylamine hydrochloride盐酸羟胺
IUPAC标准名
hydroxylamine hydrochloride
IUPAC传统名
primary amine hydrochloride
数据登录号
CAS号
Beilstein号
默克索引号
化合物性质
安全信息
GHS危险品标识
GHS05
腐蚀金属,类别1
腐蚀皮肤,类别1A,1B,1C
严重眼损伤,类别1
GHS09
对水环境的危害
急性危害,类别1
慢性危害,类别1,2
GHS07
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
GHS01
不稳定的炸药
不稳定的炸药
不稳定的炸药
有机过氧化物,类别A、B
GHS08
呼吸道过敏,类别1
生殖细胞突变,类别1A,1B,2
致癌性,类别1A,1B,2
生殖毒性,类别1A,1B,2
特定目标器官毒性 – 一次接触,类别1,2
特定目标器官毒性 – 反复接触,类别1,2
吸入危险,类别1
RTECS编号
NC3675000
联合国危险货物包装类别(PG)
III
联合国危险货物等级
8
GHS危险声明
H200-H351-H373-H290-H315-H319-H400-H302-H312-H317
欧盟危险性物质标志
环境危害性 环境危害性 (N)
爆炸性 爆炸性 (E)
有害性 有害性 (X)
保存注意事项
Hygroscopic
GHS警示性声明
P280H-P273-P406
安全公开号
36/37-61
TSCA收录
危险公开号
2-21/22-36/38-40-43-48/22-50
联合国危险货物编号
UN2923
理化性质
熔点
152°C dec.
密度
1.67
产品相关信息
纯度
99%
描述信息
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分子图谱
暂无数据
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参考文献
• For examples of preparation of oximes from carbonyl compounds, see: Org. Synth. Coll., 2, 70, 313 (1955); 7, 149 (1990). Dehydration of aldoximes is a valuable route to nitriles. The preparation of an oxime, and dehydration with acetic anhydride, are exemplified for veratraldehyde: Org. Synth. Coll., 2, 622 (1943). For other methods of dehydrating oximes to nitriles, see Benzaldoxime, A12053. Procedures for the one-pot conversion of aldehydes to nitriles, without isolation of the intermediate oxime, include: refluxing the aldehyde with hydroxylamine hydrochloride in formic acid/ sodium acetate: J. Chem. Soc., 1564 (1965); formic acid alone: Synthesis, 112 (1979); in pyridine and toluene, with azeotropic water removal: Synthesis, 190 (1982); in DMF (reflux; aromatics only): Z. Chem., 15, 302 (1975); heating in NMP at 110-115o, effective for aromatic and aliphatic substrates; under these conditions, DMF gave only 20-30% conversion: Synthesis, 586 (1999). A more recent ambient temperature one-pot procedure utilizes DBU in combination with ethyl dichlorophosphate: Synlett, 1317 (2007).
• For a brief feature on uses of this reagent in Organic synthesis, see: Synlett, 1326 (2007).
• For a one-pot synthesis of pyrazoles from aldehydes by cyclization of the intermediate oxime in acidic medium with potassium dihyrogen phosphate, see: Tetrahedron Lett., 47, 43 (2006).