6225-10-1

Basic information

• Product Name: N-METHYLVALERAMIDE
• Synonyms: N-METHYLVALERAMIDE;N-Methylpentanamide;N-Methylvaleramide,98%
• CAS NO: 6225-10-1
• Molecular Formula: C₆H₁₃NO
• Molecular Weight: 115.17
• Mol File: 6225-10-1.mol
• Article Data: 1

Chemical Properties

• Melting Point: -26°C
• Boiling Point: 116-118°C 8mm
• Flash Point: >100°C
• Appearance: /
• Density: 0,9 g/cm3
• Vapor Pressure: 0.136mmHg at 25°C
• Refractive Index: 1.4410
• BRN: 1741878
• CAS DataBase Reference: N-METHYLVALERAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-METHYLVALERAMIDE(6225-10-1)
• EPA Substance Registry System: N-METHYLVALERAMIDE(6225-10-1)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 6225-10-1(Hazardous Substances Data)

Usage

Uses

N-Methylvaleramide is used to study thermodynamics of carboxylic acids, amines and N-substituted amides in aqueous solution.

InChI:InChI=1/C6H13NO/c1-3-4-5-6(8)7-2/h3-5H2,1-2H3,(H,7,8)

Upstream product

• 591-78-6 n-hexan-2-one 

Downstream Products

• 3301-90-4 6-ethyl-tetrahydro-2H-pyran-2-one 
• 105-21-5 4-propylbutanolide 
• 111-14-8 oenanthic acid 
• 25419-06-1 N-methylpentylamine 
• 108-29-2 5-methyl-dihydro-furan-2-one 
• 107-92-6 butyric acid 
• 854659-33-9 1-(2,4-dimethoxyphenyl)pentan-1-one 
• 126118-89-6 2-(n-butyl)-5-phenyl-1,3,4-thiadiazole 
• 16451-26-6 N-methyl-N-nitrosovaleramide 

Relevant articles and documents

Silica sulfuric acid as a reusable catalyst for the conversion of ketones into amides by a Schmidt reaction under solvent-free conditions

Silica sulfuric acid is a highly efficient reagent for the conversion of a variety of ketones into the corresponding amides by a Schmidt reaction under solvent-free conditions. Cyclic, aliphatic and aromatic ketones with electron-donating or withdrawing substituents may be converted easily in excellent yield. The major advantages of this method are: operational simplicity, the ready availability of the reagent, selectivity, general applicability, mild reaction conditions, short reaction times and high yields. The recovered catalyst could be used in new attempts without any purification.