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99-51-4

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99-51-4 Usage

Description

4-Nitro-o-xylene, also known as 1,2-dimethyl-4-nitrobenzene, is an organic compound that appears as yellow prisms or yellow crystalline solid. It is a derivative of xylene, with a nitro group attached to the para position of the benzene ring. This chemical possesses specific chemical properties that make it suitable for various applications across different industries.

Uses

Used in Chemical Synthesis Industry:
4-Nitro-o-xylene is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its chemical structure allows for further functionalization and modification, making it a versatile building block for the development of new molecules with potential applications in medicine, agriculture, and other fields.
Used in Dye and Pigment Industry:
4-Nitro-o-xylene is utilized as a starting material for the production of dyes and pigments. Its ability to form colored compounds upon chemical reactions makes it a valuable component in the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Rubber and Plastics Industry:
In the rubber and plastics industry, 4-Nitro-o-xylene is employed as a chemical intermediate for the production of antioxidants and stabilizers. These additives are crucial for improving the durability, resistance to heat and light, and overall performance of rubber and plastic materials.
Used in Agrochemical Industry:
4-Nitro-o-xylene serves as a precursor in the synthesis of agrochemicals, such as herbicides and insecticides. Its role in the production of these compounds contributes to the development of effective solutions for pest control and crop protection, ensuring higher yields and better quality agricultural products.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

4-Nitro-o-xylene is incompatible with strong oxidizers and strong bases.

Fire Hazard

4-Nitro-o-xylene is combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 99-51-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99-51:
(4*9)+(3*9)+(2*5)+(1*1)=74
74 % 10 = 4
So 99-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c1-6-3-4-8(9(10)11)5-7(6)2/h3-5H,1-2H3

99-51-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L05342)  4-Nitro-o-xylene, 99%   

  • 99-51-4

  • 100g

  • 215.0CNY

  • Detail
  • Alfa Aesar

  • (L05342)  4-Nitro-o-xylene, 99%   

  • 99-51-4

  • 500g

  • 942.0CNY

  • Detail
  • Aldrich

  • (N28604)  1,2-Dimethyl-4-nitrobenzene  99%

  • 99-51-4

  • N28604-100G

  • 411.84CNY

  • Detail

99-51-4SDS

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-Nitro-o-xylene

1.2 Other means of identification

Product number -
Other names 1,2-dimethyl-4-nitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:99-51-4 SDS

99-51-4Relevant articles and documents

Photoinduced Iron-Catalyzed ipso-Nitration of Aryl Halides via Single-Electron Transfer

Wu, Cunluo,Bian, Qilong,Ding, Tao,Tang, Mingming,Zhang, Wenkai,Xu, Yuanqing,Liu, Baoying,Xu, Hao,Li, Hai-Bei,Fu, Hua

, p. 9561 - 9568 (2021/08/06)

A photoinduced iron-catalyzed ipso-nitration of aryl halides with KNO2 has been developed, in which aryl iodides, bromides, and some of aryl chlorides are feasible. The mechanism investigations show that the in situ formed iron complex by FeSO4, KNO2, and 1,10-phenanthroline acts as the light-harvesting photocatalyst with a longer lifetime of the excited state, and the reaction undergoes a photoinduced single-electron transfer (SET) process. This work represents an example for the photoinduced iron-catalyzed Ullmann-type couplings.

Cyhalofop-containing pesticide composition and application thereof

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Paragraph 0016; 0035; 0040-0041; 0046; 0051-0052; 0057; ...., (2021/11/26)

The invention discloses a pesticide composition containing cyhalofop-butyl and application thereof, belongs to the technical field of pesticide preparation and comprises 10 - 20 parts of cyhalofop-butyl. Tetramethyl chloride 3-5 parts, synergistic microcapsule 8-13 parts, wetting agent 1.5 - 4.5 parts, dispersing agent 1-3 parts, defoaming agent 0.5 - 1.5 parts and water 40 - 50 parts. When the water in the soil is less, the weed is absorbed by the chitosan so as to accelerate the absorption of A the synergic microcapsule and the cyhalofop-butyl ester, so that the pesticide composition is greatly reduced per mu.

Method and device for preparing methylnitro-benzene by channelization

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Paragraph 0047; 0048; 0049, (2019/02/04)

The invention discloses a method and a device for preparing methylnitro-benzene by channelization. The device comprises a storage tank, a nitrogen dioxide cylinder, an ozone generator, a flow pump, agas flowmeter, a reaction pipeline filled with a catalyst, a mixing pipeline, two T-shaped mixed joints, a cooling system, a heating system, a back pressure valve and a receiving tank. The method specifically comprises the following steps: opening the cooling system and the heating system; opening the ozone generator; arranging the flow pump and the gas flowmeter; and mixing raw materials liquid methyl benzene and nitrogen dioxide through the first T-shaped mixing joint and feeding the mixture into the mixing pipeline, then mixing the mixture with ozone in the second T-shaped mixing joint, feeding the mixture into the reaction pipeline filled with the catalyst for a nitrifying reaction, and post-treating a reaction liquid to obtain methylnitro-benzene. The method is controlled precisely and automatically, and is simple to operate, mild in reaction condition, simple in post treatment, quick to transfer mass and heat, high in safety and good in economical benefit.

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