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13180

苄胺

Name: 苄胺
Brand: SIAL

derivatization grade (GC derivatization), LiChropur^™, ≥99.0%

别名:

α-氨基甲苯

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关于此项目

线性分子式:

C₆H₅CH₂NH₂

化学文摘社编号:

100-46-9

分子量:

107.15

NACRES:

NA.22

PubChem Substance ID:

329750088

eCl@ss:

39030404

UNSPSC Code:

23151817

EC Number:

202-854-1

MDL number:

MFCD00008106

Beilstein/REAXYS Number:

741984

Assay:

≥99.0% (GC), ≥99.0%

Form:

liquid

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属性

grade

derivatization grade (GC derivatization)

Quality Level

100

assay

≥99.0% (GC), ≥99.0%

form

liquid

quality

LiChropur^™

technique(s)

gas chromatography (GC): suitable

refractive index

n20/D 1.543

bp

184-185 °C (lit.)

mp

10 °C (lit.)

solubility

H₂O: soluble

density

0.981 g/mL at 25 °C (lit.)

SMILES string

NCc1ccccc1

InChI

1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2

InChI key

WGQKYBSKWIADBV-UHFFFAOYSA-N

说明

General description

苄胺是一种伯胺化合物，可作为荧光衍生化试剂，通过色谱-荧光检测法灵敏且选择性地测定分析物。

Application

用高效液相色谱 (HPLC) —荧光检测法测定生物样品中的5-羟基吲哚、儿茶酚胺和儿茶酚之前，可使用苄胺作为衍生化试剂来提高灵敏度

Other Notes

探索最适于 HPLC 或 LC-MS 分析的 LiChropur^™ 试剂

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302 + H312,H314

pcodes

P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P362 + P364

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

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Synthesis of unsaturated seven-membered ring lactams through palladium-catalyzed amination and intramolecular cyclocarbonylation reactions of amines and Baylis-Hillman acetates.

Hong Cao et al.

Organic letters, 13(1), 11-13 (2010-12-02)

A versatile synthesis of unsaturated seven-membered ring lactams has been developed. The sequence involves hydroamination of Baylis-Hillman acetate with amines, followed by intramolecular cyclocarbonylation reactions of the resulting allylamines. This process can tolerate a wide array of functional groups, and

O-Hydroxyl- or o-amino benzylamine-tacrine hybrids: multifunctional biometals chelators, antioxidants, and inhibitors of cholinesterase activity and amyloid-β aggregation.

Fei Mao et al.

Bioorganic & medicinal chemistry, 20(19), 5884-5892 (2012-09-05)

In an effort to identify novel multifunctional drug candidates for the treatment of Alzheimer's disease (AD), a series of hybrid molecules were synthesised by reacting N-(aminoalkyl)tacrine with salicylic aldehyde or derivatives of 2-aminobenzaldehyde. These compounds were then evaluated as multifunctional

One-pot triple functionalization of carbon nanotubes.

Cécilia Ménard-Moyon et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 17(11), 3222-3227 (2011-02-11)

Carbon nanotubes (CNTs) are very promising as carriers for the delivery of bioactive molecules. The multifunctionalization of CNTs is necessary to impart multimodalities for the development of future CNT-based multipotent therapeutic constructs. In this context, we report the first example

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货号	GTIN
13180-100ML	04061838728586
13180-10X1ML	04061838195487
13180-1ML-KC	04061838089243
13180-500ML	04061838728593