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Merck
CN

101915

2,4-二氨基甲苯

98%

别名:

4-甲基间苯二胺, 2,4-二氨基甲苯, 2,4-甲苯二胺, 4-甲基-1,3-苯二胺

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关于此项目

线性分子式:
CH3C6H3(NH2)2
化学文摘社编号:
分子量:
122.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-453-1
Beilstein/REAXYS Number:
2205839
MDL number:
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产品名称

2,4-二氨基甲苯, 98%

SMILES string

Cc1ccc(N)cc1N

InChI key

VOZKAJLKRJDJLL-UHFFFAOYSA-N

InChI

1S/C7H10N2/c1-5-2-3-6(8)4-7(5)9/h2-4H,8-9H2,1H3

assay

98%

form

solid

bp

283-285 °C (lit.)

mp

97-99 °C (lit.)

Quality Level

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Application

  • 采用UV/H2O2工艺降解合成废水中的2,4-二氨基甲苯:该研究探讨了采用UV/H2O2 工艺降解合成废水中的致癌性2,4-二氨基甲苯,重点关注其改进水处理方法的潜力(J Hosseini, A Shokri, 2017)。
  • 用于2,4 -二硝基甲苯氢化的磁性铁氧体负载钯催化剂的开发:该论文讨论了使用Pd/NiFe2O4催化剂将2,4 -二硝基甲苯高效地氢化为2,4-二氨基甲苯,显示了高产率和工业应用潜力(V Hajdu, M Varga, G Muránszky, G Karacs, 2021)。
  • 苦味酸和2, 3-二氨基甲苯、 2, 4-二氨基甲苯形成的不敏感含能盐(insensitive energetic salt)的合成、表征和能量性能:该论文展示了新含能材料的合成和表征,该材料可能对更安全的炸药和烟火装置的开发很重要(N Şen, H Nazir, N Atҫeken, KS Hope, N Acar, 2020

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 1B - Muta. 2 - Repr. 2 - Skin Sens. 1 - STOT RE 2

target_organs

Liver,Kidney

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

320.0 °F - closed cup

flash_point_c

160 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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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Kazunori Narumi et al.
Mutation research, 747(2), 234-239 (2012-06-09)
Various liver micronucleus assay methods, such as those involving partial hepatectomy, treatment with mitogens, and the use of juvenile animals, have been developed. These assays have been proven to be of high sensitivity and specificity to predict hepatocarcinogenicity of compounds
Pei-Shan Liu et al.
Toxicology, 219(1-3), 167-174 (2005-12-13)
Toluene diisocyanate (TDI) is widely used as a chemical intermediate in the production of polyurethane. TDI-induced asthma is related to its disturbance of acetylcholine activity in most affected workers, but the relevant mechanisms are unclear. Toluene diamine (TDA) is the
Isabelle Séverin et al.
Toxicology, 213(1-2), 138-146 (2005-07-06)
2,4-Diaminotoluene (2,4-DAT) is a widely used industrial intermediate and human exposure is possible in the dye and plastics industries. We investigated the genotoxicity of the environmental pollutant, 2,4-DAT, in human HepG2 cells using the unscheduled DNA synthesis (UDS) test, the
Astrid Rohrbeck et al.
Toxicological sciences : an official journal of the Society of Toxicology, 118(1), 31-41 (2010-08-18)
Information on the carcinogenic potential of chemicals is primarily available for High Production Volume (HPV) products. Because of the limited knowledge gain from routine cancer bioassays and the fact that HPV chemicals are tested only, there is the need for
Jeroen A J Vanoirbeek et al.
Toxicological sciences : an official journal of the Society of Toxicology, 109(2), 256-264 (2009-04-01)
Toluene diamine (TDA) is formed when toluene diisocyanate (TDI), a potent sensitizer, comes in contact with an aqueous environment. The sensitizing capacity of TDA and the cross-reactivity between TDI and TDA are unknown. TDA (5-25%) and TDI (0.3%), dissolved in

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