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Merck
CN

78750

Supelco

异氰酸苯酯

derivatization grade (HPLC), LiChropur, ≥99.0% (GC)

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线性分子式:
C6H5NCO
化学文摘社编号:
分子量:
119.12
Beilstein:
471391
EC 号:
MDL编号:
UNSPSC代码:
41115716
PubChem化学物质编号:
NACRES:
NA.22
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等级

derivatization grade (HPLC)

质量水平

蒸汽压

1.4 mmHg ( 20 °C)

方案

≥99.0% (GC)

表单

liquid

质量

LiChropur

技术

HPLC: suitable

折射率

n20/D 1.535 (lit.)
n20/D 1.536

沸点

162-163 °C (lit.)

mp

−30 °C (lit.)

密度

1.096 g/mL at 25 °C (lit.)

SMILES字符串

O=C=Nc1ccccc1

InChI

1S/C7H5NO/c9-6-8-7-4-2-1-3-5-7/h1-5H

InChI key

DGTNSSLYPYDJGL-UHFFFAOYSA-N

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一般描述

Phenyl isocyanate is an aromatic monoisocyanate which is a constituent of diphenyl methane diisocyanate. It is suitable to make aryl ureas with amine at room temperature making it unlikely to detect isocyanate formation using NMR. It reacts with amino acids in alkaline solution and with peptone.

应用

Phenyl isocyanate was used in preparing grapheme-polymer nanocomposites by mixing exfoliated phenyl isocyanate-treated graphite oxide sheets with polystyrene. It was used in studying its reaction of o-hydroxybenzyl alcohol in polar solvents with in situ FT-IR which showed that phenolic hydroxyl group reacts easily than aliphatic hydroxyl group.

其他说明

用于测定醇和胺的试剂
Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Corr. 1C - Skin Sens. 1A - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

123.8 °F - closed cup

闪点(°C)

51 °C - closed cup

个人防护装备

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

法规信息

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分析证书(COA)

Lot/Batch Number

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访问文档库

B. Bjorkqvist et al.
Journal of Chromatography A, 204, 109-109 (1981)
The reaction of o-hydroxybenzyl alcohol with phenyl isocyanate in polar solvents.
De Han, Yong, et al.
Reaction Kinetics, Mechanisms and Catalysis, 101, 41-48 (2010)
Phenyl isocyanate protein compounds and their immunological properties.
S J Hopkins et al.
The Biochemical journal, 27(3), 740-753 (1933-01-01)
Marc Hutchby
Novel Synthetic Chemistry of Ureas and Amides, 62-62 (2012)
Graphene-based composite materials.
Stankovich, Sasha, et al.
Nature, 442, 282-286 (2006)

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