10097-06-0

Basic information

• Product Name: Urea,N,N''-(4-methyl-1,3-phenylene)bis- (9CI)
• Synonyms: Urea,1,1'-(4-methyl-m-phenylene)di- (7CI,8CI); Dyhard RU 500
• CAS NO: 10097-06-0
• Molecular Formula: C9H12 N4 O2
• Molecular Weight: 208.22
• Mol File: 10097-06-0.mol

Chemical Properties

• CAS DataBase Reference: Urea,N,N''-(4-methyl-1,3-phenylene)bis- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Urea,N,N''-(4-methyl-1,3-phenylene)bis- (9CI)(10097-06-0)
• EPA Substance Registry System: Urea,N,N''-(4-methyl-1,3-phenylene)bis- (9CI)(10097-06-0)

Safety Data

• Hazardous Substances Data: 10097-06-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Urea,N,N''-(4-methyl-1,3-phenylene)bis(9CI) is used as an active pharmaceutical ingredient for the development of various medications. Its unique chemical structure allows it to interact with biological targets, making it a valuable component in drug discovery and formulation.
Used in Cosmetics and Personal Care Industry:
In the cosmetics and personal care industry, Urea,N,N''-(4-methyl-1,3-phenylene)bis(9CI) is used as a stabilizer to maintain the quality and consistency of products. Its ability to prevent degradation and ensure product longevity makes it an essential ingredient in formulations.
Used in Industrial Processes:
Urea,N,N''-(4-methyl-1,3-phenylene)bis(9CI) is utilized in the production of resins and polymers, contributing to the development of various materials with specific properties. Its role in these processes highlights its versatility and importance in the chemical industry.

Upstream product

• 590-28-3 potassium cyanate 
• 95-80-7 4-methylbenzene-1,3-diamine 
• 584-84-9 2,4-Toluene diisocyanate 
• 7664-41-7 ammonia 
• 7664-93-9 sulfuric acid 
• 7450-62-6 2,4-bis-(ethoxycarbonylamino)toluene 
• 57-13-6 urea 

Downstream Products

• 95-80-7 4-methylbenzene-1,3-diamine 
• 7664-41-7 ammonia 
• 108-80-5 isocyanuric acid 
• 67768-75-6 toluene-2,4-di(carbamic acid (4-tert-butylphenyl) ester) 
• 1267645-90-8 toluene-2,4-di(carbamic acid (3,5-dimethoxyphenyl) ester) 
• 29455-59-2 toluene-2,4-di(carbamic acid (2-naphthyl) ester) 
• 1266555-71-8 C₃₃H₂₆N₂O₆ 
• 52820-04-9 4-methyl-1,3-phenylenedi(carbamic acid(4-nonylphenyl)ester) 
• 584-84-9 2,4-Toluene diisocyanate 
• 52820-06-1 toluene-2,4-di(carbamic acid (4-cumylphenyl) ester) 
• 1267645-86-2 toluene-2,4-di(carbamic acid (4-(1,1,3,3-tetramethylbutyl)phenyl) ester) 
• 4223-24-9 toluene-2,4-dicarbamic acid diphenyl ester 
• 25635-03-4 1,1'-(4-methyl-1,3-phenylene)bis(3-ethylurea) 

Relevant articles and documents

A urea french ion liquid catalysis method for preparing toluene diisocyanate

The invention provides application of an ionic liquid in preparing toluene diisocynate and a method for preparing the toluene diisocynate from urea under the catalysis of the ionic liquid. The method is used for preparing the toluene diisocynate by taking toluenediamine and urea as the raw materials, reacting the raw materials to generate toluene diurea under the catalytic action of the ionic liquid and then pyrolyzing the toluene diurea. The method does not need highly toxic phosgene and an extra solvent; the ionic liquid is adopted as a catalyst; on one hand, the ionic liquid is good in catalytic effect, easy to remove and environment-friendly, and on the other hand, a metal catalyst in the prior art is not used, so that the reaction of the method for preparing the toluene diisocynate from urea under the catalysis of the ionic liquid does not require harsh device materials and operating conditions, consequently, the production cost is greatly reduced, and the method is advantageous to industrial application.

A manufacturing method of a compound having a ureidopirimidine

PROBLEM TO BE SOLVED: To obtain a compound having a ureido group useful as an intermediate for producing an isocyanate, without producing by-products, which are produced in conventional production processes, and in a high yield and high purity. SOLUTION: An organic primary amine of formula (1) and urea are subjected to ureidization reaction in the presence of an aromatic hydroxylcompound of formula (2). In the formula (1), R1is a 1-35C organic group, and a is 1 to 10. In the formula (2), A is a 6-50C organic group having an aromatic ring, and the organic group is replaced with b aromatic hydroxyl groups, and b is 1 to 3. COPYRIGHT: (C)2012,JPOandINPIT

METHOD FOR PRODUCING COMPOUND HAVING UREIDO GROUP

PROBLEM TO BE SOLVED: To provide a method for producing a compound having a ureido group capable of obtaining a compound having a ureido group useful as an intermediate in producing an isocyanate in a short time with a high yield and high purity while sup

Method for Producing Carbonyl Compund

A method for producing a carbonyl compound of the present invention comprises a step (X) of reacting a specific compound having a urea bond with a carbonic acid derivative having a carbonyl group (—C(═O)—) under heating at a temperature equal to or higher

PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER

The present invention provides a method for producing N-substituted carbamic acid-O-aryl ester derived from a compound having an ureido group, the method comprising the step of carrying out esterification or esterification and transesterification from the compound having the ureido group and a hydroxy composition containing one type or a plurality of types of hydroxy compounds.