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N-异丙基-N-甲基叔丁胺

N-异丙基-N-甲基叔丁胺名称

[ CAS 号 ]:
85523-00-8

[ 中文名 ]:
N-异丙基-N-甲基叔丁胺

[ 英文名 ]:
n-isopropyl-n-methyl-tert-butylamine

[英文别名 ]:

N-isopropyl-N-methyl-butylamine
N-isopropyl-N-methyl-t-butylamine
tert-butyl-N-methyl-N-isopropylamine
N-tert.-Butyl-N-methyl-N-isopropylamin
Methyl-isopropyl-tert.-butyl-amin
tert-butylisopropylmethylamine
N-Isopropyl-N-methyl-tert-butylamine

N-异丙基-N-甲基叔丁胺物理化学性质

[ 密度 ]:
0.767 g/mL at 25ºC(lit.)

[ 沸点 ]:
127ºC(lit.)

[ 熔点 ]:
-76.53°C (estimate)

[ 分子式 ]:
C₈H₁₉N

[ 分子量 ]:
129.24300

[ 闪点 ]:
49 °F

[ 精确质量 ]:
129.15200

[ PSA ]:
3.24000

[ LogP ]:
2.12510

[ 折射率 ]:
n20/D 1.419(lit.)

[ 储存条件 ]:
室温

N-异丙基-N-甲基叔丁胺MSDS

N-异丙基-N-甲基叔丁胺安全信息

[ 符号 ]:

GHS02, GHS07

[ 信号词 ]:
Danger

[ 危害声明 ]:
H225-H315-H319-H335

[ 警示性声明 ]:
P210-P261-P305 + P351 + P338

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
F,Xi

[ 风险声明 (欧洲) ]:
11-36/37/38

[ 安全声明 (欧洲) ]:
16-26-36

[ 危险品运输编码 ]:
UN 1993 3/PG 2

[ WGK德国 ]:
3

[ 海关编码 ]:
2921199090

N-异丙基-N-甲基叔丁胺合成路线

N-异丙基-N-甲基叔丁胺上下游产品

N-异丙基-N-甲基叔丁胺上游产品

N-异丙基-N-甲基叔丁胺下游产品

N-异丙基-N-甲基叔丁胺海关

[ 海关编码 ]: 2921199090

[ 中文概述 ]:
2921199090 其他无环单胺及其衍生物及其盐。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

N-异丙基-N-甲基叔丁胺文献

Towards a Second Generation of Ionic Liquid Matrices (ILMs) for MALDI-MS of Peptides, Proteins, and Carbohydrates

J. Am. Soc. Mass Spectrom. 20 , 1790-1800, (2009)

Second generation ionic liquid matrices are developed, examined, and tested. They have shown a wide mass detection range (<1000 Da to >270,000 Da) for proteins and peptides with greater S/N ratios tha...

Recent advances in the synthesis of ammonium-based rotaxanes.

Molecules 15(5) , 3709-30, (2010)

The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rath...

Asymmetric synthesis of primary amines via the spiroborate-catalyzed borane reduction of oxime ethers.

Org. Lett. 9(9) , 1793-5, (2007)

[reaction: see text] The enantioselective borane reduction of O-benzyloxime ethers to primary amines was studied under catalytic conditions using the spiroborate esters 5-10 derived from nonracemic 1,...

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