25347-94-8

Basic information

• Product Name: 1-tert-butyl-3-methylurea
• CAS NO: 25347-94-8
• Molecular Formula: C₆H₁₄N₂O
• Molecular Weight: 130.1882
• Mol File: 25347-94-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 249.3°C at 760 mmHg
• Flash Point: 111.5°C
• Density: 0.914g/cm³
• Vapor Pressure: 0.0231mmHg at 25°C
• Refractive Index: 1.433
• CAS DataBase Reference: 1-tert-butyl-3-methylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tert-butyl-3-methylurea(25347-94-8)
• EPA Substance Registry System: 1-tert-butyl-3-methylurea(25347-94-8)

Safety Data

• Hazardous Substances Data: 25347-94-8(Hazardous Substances Data)

Usage

Type of compound

Urea derivative (specifically, a substituted urea)

Substituent groups

A tert-butyl group and a methyl group attached to the nitrogen atom

Common uses

Reagent in organic synthesis, pharmaceutical research

Potential applications

Corrosion inhibitor, stabilizer for explosives

Biological properties

Antifungal and antiviral properties

Importance

Versatile and valuable in scientific and industrial applications

Upstream product

• 75-64-9 tert-butylamine 
• 624-83-9 methyl isocyanate 
• 95598-14-4 3-t-butyl-1-methyl-1-nitrosothiourea 
• 10016-20-3 alpha cyclodextrin 
• 19411-70-2 N-tert-butyl-N'-methylcarbodiimide 
• 3964-50-9 N-methyl-N'-tert-butylthiourea 

Downstream Products

• 36801-14-6 1-Benzoyl-3-methyl-5-tert-butylbiuret 
• 72479-14-2 N-Methyl-N'-tert-butyl-N-nitrosourea 
• 80820-72-0 1-tert-Butyl-3-methyl-5-(4-tolyl)biuret 
• 80820-86-6 1-tert-Butyl-3-methyl-5-(2-tolyl)biuret 
• 36791-65-8 N-tert-butyl-3-methyl-N'-(4-nitro-phenyl)-[1,3]thiazetidine-2,4-diylidenediamine 
• 590-42-1 tert-butyl isothiocyanate 
• 23730-18-9 4-methyl-N-(tert-butylcarbamoyl)benzenesulfonamide 
• 36801-13-5 N-(3-tert-Butyl-1,2-dimethyl-isoureidocarbonyl)-benzamide 
• 36791-67-0 N-(4-tert-butylimino-3-methyl-[1,3]thiazetidin-2-ylidene)-toluene-4-sulfonamide 

Relevant articles and documents

An empirical estimation of the interactions Hδ+...Cl-. The crystal and molecular structure of the 1-methyl-2-tert-butylamino-4-isopropyl-5(4H)-imidazolone hydrochloride

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SUPPRESSION OF THE CONVERSION OF 3-t-BUTYL-1-METHYL-1-NITROSOTHIOUREA TO 3-t-BUTYL-1-METHYLUREA BY β-CYCLODEXTRIN UNDER ACIDIC CONDITIONS

The denitrosation of 3-t-butyl-1-methyl-1-nitrosothiourea (1) was retarded by β-, and γ-cyclodextrins (CDs) at pH 4.70.Decomposition of 1 in the presence of β-CD produced selectively 3-t-butyl-1-methylthiourea (1a), which was remarkably different from the product ratio in the absence of β-CD.These results may be caused by both the protective and the microsolvent effect of β-CD.

THE SYNTHESIS OF ANTINEOPLASTIC AGENTS. XXXII. N-NITROSOUREAS. I.

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