102253
2,5-二甲基苯胺
99%
别名:
2,5-二甲苯胺, 2-氨基-1,4-二甲苯, 2-氨基对二甲苯
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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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-451-0
Beilstein/REAXYS Number:
2205178
MDL number:
产品名称
2,5-二甲基苯胺, 99%
InChI key
VOWZNBNDMFLQGM-UHFFFAOYSA-N
InChI
1S/C8H11N/c1-6-3-4-7(2)8(9)5-6/h3-5H,9H2,1-2H3
SMILES string
Cc1ccc(C)c(N)c1
assay
99%
refractive index
n20/D 1.559 (lit.)
bp
218 °C (lit.)
mp
11.5 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
Quality Level
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Application
2,5-二甲基苯胺可用于合成嵌入聚（2,5-二甲基苯胺）中的多壁碳纳米管的纳米复合材料。 2,5-二甲基苯胺可用于研究真菌通过2,5-二甲苯胺形成的代谢产物对漆酶活性的影响。
General description
2,5-二甲基苯胺是一种无色至暗黄色、无色至棕色的液体。它是真菌漆酶的底物。2,5-二甲基苯胺可在无水NH4F·2.35 HF介质中进行电化学氧化，形成导电聚合物，聚（2,5-二甲基苯胺）。铜基材上的聚（2,5-二甲基苯胺）涂层可保护铜免受腐蚀。2,5-二甲基苯胺的傅里叶变换红外光谱（FTIR）和拉曼光谱已有研究。它可诱导lccIV的转录。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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Thomas Bertrand et al.
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Journal of biomolecular structure & dynamics, 27(4), 501-510 (2009-11-18)
Laccases are polyphenol oxidases which oxidize a broad range of reducing substrates, preferably phenolic compounds, and their use in biotechnological applications is increasing. Recently, the first X-ray structure of active laccase from white rot fungus Rigidoporus lignosus has been reported
Albert Kollmann et al.
Applied microbiology and biotechnology, 68(2), 251-258 (2005-01-14)
Numerous chemicals, including the xenobiotic 2,5-xylidine, are known to induce laccase production in fungi. The present study was conducted to determine whether the metabolites formed from 2,5-xylidine by fungi could enhance laccase activity. We used purified laccases to transform the
Oxidation of 2, 5-dimethylaniline in NH 4 F? 2.35 HF medium Characteristics of the resulting conducting polymer.
Genies EM and Noel P.
J. Electroanal. Chem. Interfac. Electrochem., 296(2), 473-490 (1990)
Jai Kishan Ojha et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 632-643 (2012-08-08)
The Fourier transform infrared (FTIR) and Raman spectra of 2-amino-4-nitrotoluene; 2-amino-5-nitrotoluene; 2,4-dimethylaniline; 2,5-dimethylaniline; 2,6-dimethylaniline; 1,2,4-trimethylbenzene; 1,3,5-trimethylbenzene and pentamethylbenzene have been recorded in the range 4000-400 cm(-1) and 4000-30 cm(-1), respectively. A normal coordinate analysis was carried out for both in-plane
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