物质信息

ID:718684

名称和标识
别名
MethenamineHexamineHexamethylenetetramine六亚甲基四胺
IUPAC传统名
methenamine
IUPAC标准名
1,3,5,7-tetraazatricyclo[3.3.1.13,7]decane
数据登录号
Beilstein号
CAS号
默克索引号
化合物性质
安全信息
GHS危险声明
H228-H302-H317
保存注意事项
Hygroscopic
危险公开号
11-43
联合国危险货物等级
4.1
联合国危险货物包装类别(PG)
III
GHS危险品标识
GHS02
易燃气体类别1
易燃气溶胶,第1,2类
易燃液体,类别1,2,3
自反应物质和混合物,类型B,C,D,E,F
自燃液体类别1
自燃固体类别1
自我放热物质和混合物,类别1,2
与水接触的物质和混合物,放出易燃气体类别1,2,3
有机过氧化物,类别B,C,D,E,F
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
联合国危险货物编号
UN1328
RTECS编号
MN4725000
TSCA收录
欧盟危险性物质标志
易燃性 易燃性 (F)
刺激性 刺激性 (Xi)
安全公开号
24-37
GHS警示性声明
P210-P241-P261-P302+P352-P321-P501A
理化性质
密度
1.33
熔点
ca 280°C subl.
闪点
250°C(482°F)
产品相关信息
纯度
99+%
描述信息
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分子图谱
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参考文献
• The reaction can also be carried out to give the primary amine on hydrolysis (Delepine reaction). For conversion of allylic halides to amines, see, e.g.: Org. Synth. Coll., 5, 121 (1973); 9, 666 (1998).
• For a review of applications in organic synthesis, see: Synthesis, 161 (1979).
• Formylation of arylamines and phenols in the presence of acid to give aldehydes (Duff reaction) generally gives low yields: J. Chem. Soc., 547 (1941); Org. Synth. Coll., 4, 866 (1963). In TFA, formylation of aromatic hydrocarbons occurs in good yield with para-selectivity: J. Org. Chem., 37, 3972 (1972). Careful control of reaction conditions enables 4-substituted phenols in TFA to be converted to either 2-formyl or 2,6-diformyl derivatives: Synthesis, 1029 (1998).
• Can be used as a Mannich reagent, e.g. for the ɑ-methylenation of ketones: Synth. Commun., 26, 1775 (1996). For example with reaction scheme, see Propiophenone, A15140.
• Benzylic halides form quaternary salts with hexamine which undergo oxidation during hydrolysis to give aldehydes (Sommelet reaction): Org. React., 8, 197 (1954); Org. Synth. Coll., 3, 811 (1955); 4, 690, 918 (1963). Benzylamines can also be converted to benzaldehydes; see e.g.: Org. Synth. Coll., 5, 668 (1973).