物质信息
ID:345261
名称和标识
IUPAC标准名
O-tert-butylhydroxylamine hydrochloride
IUPAC传统名
O-tert-butylhydroxylamine hydrochloride
别名
O-(1,1-Dimethylethyl)hydroxylamine hydrochlorideO-tert-Butylhydroxylamine hydrochloride2-Aminooxy-2-methylpropane hydrochloridetert-Butoxyamine hydrochlorideO-叔丁基羟胺 盐酸盐
化合物性质
安全信息
欧盟危险性物质标志
易燃性 (F)MSDS下载
RID/ADR
UN 1325 4.1/PG 3
德国WGK号
3
GHS危险品标识
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
GHS警示词
Warning
个人保护装置
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
联合国危险货物包装类别(PG)
3
危险公开号
11
联合国危险货物等级
4.1
GHS警示性声明
P210
联合国危险货物编号
1325
GHS危险声明
H228
产品相关信息
纯度
≥99.0% (AT)
线性分子式
(CH3)3CONH2 · HCl
理化性质
熔点
~155 °C (dec.)
描述信息
Other Notes
用于制备 N-叔丁氧基氨基酸的试剂，N-叔丁氧基氨基酸可作为 N-羟基多肽 unambiguous synthesis 的底物9
包装
1, 5 g in glass bottle
Application
Reactant involved in synthesis of biologically active molecules including:
• CGS 25966 derivatives for use as MMP inhibitors1
• Imidazolidinedione derivatives for use as antimalarial treatments2
• Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3
• Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:
• Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5
• Double allylic alkylation of indole-2-hydroxamates6
• SN2 substitution reactions at amide nitrogens7
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8
用于制备 N-叔丁氧基氨基酸的试剂，N-叔丁氧基氨基酸可作为 N-羟基多肽 unambiguous synthesis 的底物9
包装
1, 5 g in glass bottle
Application
Reactant involved in synthesis of biologically active molecules including:
• CGS 25966 derivatives for use as MMP inhibitors1
• Imidazolidinedione derivatives for use as antimalarial treatments2
• Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3
• Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:
• Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5
• Double allylic alkylation of indole-2-hydroxamates6
• SN2 substitution reactions at amide nitrogens7
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8
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参考文献
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