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Merck
CN

136964

N-异丙基苄胺

97%

别名:

N-苄基异丙胺

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线性分子式:
C6H5CH2NHCH(CH3)2
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-067-6
Beilstein/REAXYS Number:
2638437
MDL number:
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产品名称

N-异丙基苄胺, 97%

InChI key

LYBKPDDZTNUNNM-UHFFFAOYSA-N

InChI

1S/C10H15N/c1-9(2)11-8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

SMILES string

CC(C)NCc1ccccc1

assay

97%

form

liquid

drug control

Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet

refractive index

n20/D 1.502 (lit.)

bp

200 °C (lit.)

density

0.892 g/mL at 25 °C (lit.)

functional group

amine
phenyl

Quality Level

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Application

N - 异丙基苄胺用作配体,用于制备和表征(环戊二烯基)镁。它也用于合成N-亚苄基异丙胺-N-氧化物

General description

N-甲基丙基苄胺在环境温度下在甲苯中与茂金属形成胺加合物

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

161.6 °F - closed cup

flash_point_c

72 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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One-flask transformation of secondary amines to nitrones by oxidation with hydrogen peroxide mediated by triscetylpyridinium tetrakis oxodiperoxotungsto-phosphate (PCWP). Some mechanistic considerations.
Ballistreri FP, et al.
Tetrahedron, 48(40), 8677-8684 (1992)
Aibing Xia et al.
Journal of the American Chemical Society, 124(38), 11264-11265 (2002-09-19)
Magnesocene adducts of alkylamines were prepared and characterized. Treatment of 3-amino-2,4-dimethylpentane, isopropylamine, tert-butylamine, benzylamine, or N-isopropylbenzylamine with magnesocene at ambient temperature in toluene afforded the amine adducts Cp2Mg(NH2CH(CH(CH3)2)2) (91%), Cp2Mg(NH2iPr) (80%), Cp2Mg(NH2tBu) (67%), Cp2Mg(NH2CH2Ph) (80%), and Cp2Mg(NH(CH(CH3)2)(CH2C6H5)) (91%). These adducts
O Brüggemann
Biomolecular engineering, 18(1), 1-7 (2001-06-29)
Molecular imprinting is a way of creating polymers bearing artificial receptors. It allows the fabrication of highly selective plastics by polymerizing monomers in the presence of a template. This technique primarily had been developed for the generation of biomimetic materials

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