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Merck
CN

D146005

2,6-二甲基苯胺

99%

别名:

2,6-二甲苯胺, 2-氨基-1,3-二甲苯, 2-氨基间二甲苯

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关于此项目

线性分子式:
(CH3)2C6H3NH2
化学文摘社编号:
分子量:
121.18
Beilstein:
636332
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

<0.01 mmHg ( 20 °C)

质量水平

方案

99%

表单

liquid

折射率

n20/D 1.560 (lit.)

沸点

214 °C/739 mmHg (lit.)

mp

10-12 °C (lit.)

密度

0.984 g/mL at 25 °C (lit.)

SMILES字符串

Cc1cccc(C)c1N

InChI

1S/C8H11N/c1-6-4-3-5-7(2)8(6)9/h3-5H,9H2,1-2H3

InChI key

UFFBMTHBGFGIHF-UHFFFAOYSA-N

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应用

2,6-二甲基苯胺可与以下物质反应:
  • 1-萘甲醛,形成中间体双(4-氨基-3,5-二甲基苯基)萘甲烷(BADN)以进一步形成双(4-马来酰亚胺基-3,5-二甲基苯基)萘甲烷(通过与马来酸酐、乙酸酐和乙酸钠。
  • 丁基锂,形成2,6-二甲基苯胺锂,进而形成各种RhII苯胺配合物。

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

195.8 °F - closed cup

闪点(°C)

91 °C - closed cup

个人防护装备

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Reactivity of Rhodium (II) Amido/Rhodium (I) Aminyl Complexes
Zhang N, et al.
Inorgorganica Chimica Acta, 39(13), 2921-2927 (2018)
Novel bismaleimide with naphthalene side group. 1. From 1-naphthaldehyde and 2, 6-dimethylaniline
Wang CS, et al.
Polymer, 39(13), 2921-2927 (1998)
Kai Cheng et al.
Royal Society open science, 6(6), 190196-190196 (2019-07-18)
A novel aromatic diamine containing pyridyl side group, 4-pyridine-4,4-bis(3,5-dimethyl-5-aminophenyl)methane (PyDPM), was successfully synthesized via electrophilic substitution reaction. The polyimides (PIs) containing pyridine were obtained via the microwave-assisted one-step polycondensation of the PyDPM with pyromellitic dianhydride (PMDA), 3,3',4,4'-biphenyltetracarboxylic dianhydride (BPDA), 3,3',4,4'-diphenylether
Nonglak Boonrattanakij et al.
Journal of hazardous materials, 172(2-3), 952-957 (2009-08-21)
This research investigated the intrinsic second-order rate constant between 2,6-dimethyl-aniline (2,6-DMA) and hydroxyl radicals (OH) using Fenton's reactions under both batch and continuous operations. The competitive kinetics technique with aniline as a reference compound was employed. In the batch study
Wang-Ping Ting et al.
Journal of hazardous materials, 161(2-3), 1484-1490 (2008-06-17)
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed to degrade organic toxic contaminants. The use of UVA light and electric current as electron donors can efficiently initiate the

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