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1-butyl-3-ethylurea is a versatile urea derivative chemical compound characterized by the presence of a butyl group and an ethyl group attached to the nitrogen atoms of the urea molecule. This unique structure endows it with properties such as high thermal stability, low volatility, and high conductivity, positioning it as a valuable compound for a range of applications in both industrial and pharmaceutical sectors.

10310-60-8

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10310-60-8 Usage

Uses

Used in Chemical Industry:
1-butyl-3-ethylurea is used as a solvent for various chemical processes due to its ability to dissolve a wide range of substances and its compatibility with different materials.
Used in Electrochemical Applications:
In the electrochemical industry, 1-butyl-3-ethylurea serves as an electrolyte in lithium batteries, enhancing their performance and stability due to its high ionic conductivity and thermal stability.
Used in Pharmaceutical Research and Development:
1-butyl-3-ethylurea is utilized as a potential drug candidate for the treatment of neurodegenerative diseases, leveraging its unique chemical structure to target specific biological pathways and mechanisms associated with such conditions.
Each of these applications takes advantage of the distinct properties of 1-butyl-3-ethylurea, highlighting its multifaceted utility across different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 10310-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10310-60:
(7*1)+(6*0)+(5*3)+(4*1)+(3*0)+(2*6)+(1*0)=38
38 % 10 = 8
So 10310-60-8 is a valid CAS Registry Number.

10310-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-3-ethylurea

1.2 Other means of identification

Product number -
Other names 3-butyl-1-ethylurea

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:10310-60-8 SDS

10310-60-8Downstream Products

10310-60-8Relevant academic research and scientific papers

The Synthesis of N-Substituted Ureas I: The N-Alkylation of Ureas

Hackl, Kurt A.,Falk, Heinz

, p. 599 - 606 (1992)

Urea and N-alkylureas are N'-alkylated in low yields using aprotic dipolar solvents, like dimethylsulfoxide, solid potassium hydroxide, and alkyl halides.Phase transfer catalysis with tetrabutylammonium chloride in refluxing toluene results in high yield

Synthesis and application of a new fluorous-tagged ammonia equivalent

Nielsen, Simon D.,Smith, Garrick,Begtrup, Mikael,Kristensen, Jesper L.

supporting information; experimental part, p. 4557 - 4566 (2010/08/20)

A novel fluorous-tagged ammonia equivalent has been developed. It is based on a nitrogen-oxygen bond, which can be cleaved in a traceless manner by a molybdenum complex or samarium diiodide. The application in the synthesis of ureas, amides, sulfonamides, and carbamates is described. The scope of the fluo-rous N-O linker is exemplified by the synthesis of itopride, a drug used for the treatment of functional dyspepsia. Itopride was synthesized with the aid of fluorous purification methods and the product was isolated in good overall yield, with high purity.

Trapping! of isocyanates with benzotriazole in situ - Preparation of carbamoyl benzotriazoles as an isocyanate alternative via curtius rearrangement

Zhong, Zhiyun,Wang, Xiaoxia,Kong, Lichun,Zhu, Xiangming

experimental part, p. 2461 - 2464 (2010/01/07)

N-Aryl and N-alkenyl carbamoyl benzotriazoles were prepared in good to excellent yields from acyl azides and benzotriazole via Curtius rearrangement, while N-alkylcarbamoyl benzotriazoles were formed from N-alkanoyl benzotriazoles and sodium azide in one

Process for the N-alkylation or ureas

-

, (2008/06/13)

Process for the N-alkylation of ureas by reacting a urea with an alkylating agent in the presence of a solid base and a phase transfer catalyst in a diluent.

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