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5131-60-2

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5131-60-2 Usage

Description

4-Chloro-1,3-benzenediamine is a chemical compound with the molecular formula C6H7ClN2, characterized by its gray powder or dark purple solid appearance. It exhibits crystalline properties and is soluble in ethanol, slightly soluble in water, and insoluble in petroleum ether.

Uses

Used in Dye Production:
4-Chloro-1,3-benzenediamine is used as an intermediate in the dye industry for the synthesis of various dyestuffs. Its chemical structure allows for the creation of a wide range of colors and properties in dyes, making it a valuable component in this application.
Used in Rubber Processing:
In the rubber industry, 4-Chloro-1,3-benzenediamine is utilized as an additive to enhance the properties of rubber materials. It can improve the durability, strength, and resistance to wear and tear, contributing to the overall performance of rubber products.
Used in Mutagenic Effect Studies:
4-Chloro-1,3-diaminobenzene has been employed in scientific research to study the mutagenic effects of phenylenediamines, which are chemicals found in hair dyes, on Salmonella typhimurium TA 102. This application helps to understand the potential health risks associated with the use of these chemicals in the cosmetic industry and aids in the development of safer alternatives.

Air & Water Reactions

4-Chloro-1,3-benzenediamine is sensitive to prolonged exposure to light and air. Insoluble in water.

Health Hazard

ACUTE/CHRONIC HAZARDS: 4-Chloro-1,3-benzenediamine is a positive animal carcinogen and suspected human carcinogen.

Fire Hazard

Flash point data for 4-Chloro-1,3-benzenediamine are not available; however, 4-Chloro-1,3-benzenediamine is probably combustible.

Safety Profile

Suspected carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl and NOx. See also AROMATIC AMINES.

Check Digit Verification of cas no

The CAS Registry Mumber 5131-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,3 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5131-60:
(6*5)+(5*1)+(4*3)+(3*1)+(2*6)+(1*0)=62
62 % 10 = 2
So 5131-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2/c7-5-2-1-4(8)3-6(5)9/h1-3H,8-9H2

5131-60-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • Alfa Aesar

  • (A15430)  4-Chloro-m-phenylenediamine, 97%   

  • 5131-60-2

  • 5g

  • 679.0CNY

  • Detail
  • Alfa Aesar

  • (A15430)  4-Chloro-m-phenylenediamine, 97%   

  • 5131-60-2

  • 25g

  • 2672.0CNY

  • Detail
  • Aldrich

  • (125172)  4-Chloro-1,3-diaminobenzene  97%

  • 5131-60-2

  • 125172-10G

  • 994.50CNY

  • Detail

5131-60-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-1,3-benzenediamine

1.2 Other means of identification

Product number -
Other names 4-Chloro-1,3-phenylenediaMine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5131-60-2 SDS

5131-60-2Relevant articles and documents

Selective removal of nitroaromatic compounds from wastewater in an integrated zero valent iron (ZVI) reduction and ZVI/H2O2 oxidation process

Liu, Jianguo,Ou, Changjin,Han, Weiqing,Faheem,Shen, Jinyou,Bi, Huiping,Sun, Xiuyun,Li, Jiansheng,Wang, Lianjun

, p. 57444 - 57452 (2015)

In this study, an integrated system comprised of zero-valent iron (ZVI) reduction and ZVI-based Fenton oxidation processes (ZVI-ZVI/H2O2) was applied for the selective removal of nitroaromatic compounds (NACs) from 2,4-dinitroanisole (DNAN) producing wastewater. For the ZVI reduction process, at a hydraulic retention time (HRT) of 6 h and neutral pH of 7.2, removal efficiencies of 2,4-dinitroanisole (DNAN), 2,4-dinitrophenol (DNP) and 2,4-dinitrochlorobenzene (DNCB) were as high as 81.3 ± 3.6%, 80.6 ± 1.8% and 90.9 ± 3.5%, respectively, demonstrating the excellent performance of ZVI. For the ZVI/H2O2 oxidation process, the optimal pH and H2O2 dosage were found to be 3.0 and 100 mmol L-1, respectively. Under these optimal conditions, NACs and their degradation intermediates could be removed selectively and effectively in the coupled ZVI reduction and ZVI/H2O2 oxidation process, as was indicated by the low UV254 value of 0.104 ± 0.003 and the low TOC removal efficiency of 32.4 ± 0.7% in the effluent. Ferrous ions could be generated in situ through the corrosion of the metal iron in both the ZVI reduction process and the ZVI/H2O2 oxidation process, giving rise to a potent Fenton-type reaction. In addition, the enhanced Fenton reaction with the aid of reaction between Fe0 and Fe3+ was probably due to the presence of Fe0 in the ZVI/H2O2 oxidation process, which promoted the utilization efficiency of the Fenton catalyst, i.e., Fe2+. Compared to the sequential ZVI reduction and homogeneous Fenton oxidation process (ZVI-Fe2+/H2O2), the low consumption of iron shavings, the reduced H2O2 consumption and the low yield of ferric sludge made the integrated ZVI-ZVI/H2O2 process promising for the treatment of NAC containing wastewater.

CoPd Nanoalloys with Metal–Organic Framework as Template for Both N-Doped Carbon and Cobalt Precursor: Efficient and Robust Catalysts for Hydrogenation Reactions

Zhu, Jie,Xu, Deng,Ding, Lu-jia,Wang, Peng-cheng

, p. 2707 - 2716 (2021/01/21)

In this work, a series of metal–organic framework (MOF)-derived CoPd nanoalloys have been prepared. The nanocatalysts exhibited excellent activities in the hydrogenation of nitroarenes and alkenes in green solvent (ethanol/water) under mild conditions (H2 balloon, room temperature). Using ZIF-67 as template for both carbon matrix and cobalt precursor coating with a mesoporous SiO2 layer, the catalyst CoPd/NC@SiO2 was smoothly constructed. Catalytic results revealed a synergistic effect between Co and Pd components in the hydrogenation process due to the enhanced electron density. The mesoporous SiO2 shell effectively prevented the sintering of hollow carbon and metal NPs at high temperature, furnishing the well-dispersed nanoalloy catalysts and better catalytic performance. Moreover, the catalyst was durable and showed negligible activity decay in recycling and scale-up experiments, providing a mild and highly efficient way to access amines and arenes.

Efficient reduction of nitro compounds and domino preparation of 1-substituted-1H-1,2,3,4-tetrazoles by Pd(ii)-polysalophen coated magnetite NPs as a robust versatile nanocomposite

Xu, DaPeng,Xiong, Meilu,Kazemnejadi, Milad

, p. 12484 - 12499 (2021/04/14)

A new, versatile, and green methodology has been developed for the efficient NaBH4-reduction of nitroarenes as well as the domino/reduction MCR preparation of 1-substituted-1H-1,2,3,4-tetrazoles using Pd(ii)-polysalophen coated magnetite NPs as an efficient heterogeneous magnetically recyclable nanocatalyst. Polysalophen was firstly prepared based on a triazine framework with a high degree of polymerization, then coordinated to Pd ions and, finally, the resulting hybrid was immobilized on magnetite NPs. The catalyst was characterized by various instrumental and analytical methods, including GPC, DLS, N2adsorption-desorption, TGA, VSM, TEM, HRTEM, EDX, XPS, XRD, and ICP analyses. The catalyst possesses dual-functionality including the reduction of nitroarenes and the construction of tetrazole rings all in one stepviaa domino protocol. High to excellent yields were obtained for both nitro reduction and the direct preparation of 1-substituted-1H-1,2,3,4-tetrazoles from nitro compounds. Insight into the mechanism was conducted by XPSin situas well as DLSin situalong with several control experiments. Recyclability of the catalyst was studied for 6 consecutive runs along with metal leaching measurements in each cycle.

DFNS/PEI/Cu Nanocatalyst for Reduction of Nitro-aromatic Compounds

Moradi, Marjan,Rastakhiz, Nahid,Ghaedi, Mehrorang,Zhiani, Rahele

, p. 1653 - 1662 (2020/10/20)

Abstract: Nitro-aromatic pollution in industrial waste streams threat wellbeing of water resources. This study investigates the performance of a copper-based nano catalyst to reduce nitro-aromatic compounds in aqueous solution. Anchoring Cu NPs within the nano spaces of a fibrous silicate with high surface area, and simple accessibility of active sites were successfully established by a facile approach to produce a novel nanocatalyst (DFNS/PEI/Cu). DFNS displayed different properties such as dandelion-like shape, high surface area, and simple availability of active sites. Immobilization of the Cu NPs on DFNS nanospheres not only prevented their aggregation, but also considerably improved the availability of the catalytic active sites. The DFNS/PEI/Cu nanocatalyst demonstrated great catalytic activities for the reduction of nitro compounds under green conditions. Our findings show fibrous DFNS and Cu NPs as a helpful platform for the fabrication of noble metal-based affordable nanocatalyst for many catalytic applications. Graphic Abstract: DFNS/PEI/Cu nanocatalyst as a new adsorbents for the reduction of nitro compounds[Figure not available: see fulltext.]

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