673-55-2

Basic information

• Product Name: 2-(hydroxyimino)-N,N-dimethylpropan-1-amine
• CAS NO: 673-55-2
• Molecular Formula: C₅H₁₂N₂O
• Molecular Weight: 116.1616
• Mol File: 673-55-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 180.6°C at 760 mmHg
• Flash Point: 63°C
• Density: 0.94g/cm³
• Vapor Pressure: 0.413mmHg at 25°C
• Refractive Index: 1.448
• CAS DataBase Reference: 2-(hydroxyimino)-N,N-dimethylpropan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(hydroxyimino)-N,N-dimethylpropan-1-amine(673-55-2)
• EPA Substance Registry System: 2-(hydroxyimino)-N,N-dimethylpropan-1-amine(673-55-2)

Safety Data

• Hazardous Substances Data: 673-55-2(Hazardous Substances Data)

Usage

Type of compound

Synthetic chemical compound

Structural relation

Related to amphetamine

Popularity

Gained popularity as an ingredient in various dietary supplements and pre-workout products

Stimulant properties

Believed to have stimulant properties

Effects on the body

Reported to increase energy levels, focus, and mental alertness

Safety and health effects

Still under debate and banned or restricted in some countries

Potential risks

Increased heart rate, blood pressure, and the potential for addiction or dependence

Precaution

Individuals should use caution and consult with a healthcare professional before using products containing this compound.

Upstream product

• 15364-56-4 dimethylaminoacetone 
• 124-40-3 dimethyl amine 
• 92767-25-4 3-chloro-2-methyl-2-nitroso-propionaldehyde N,N'-dimer 
• 7223-38-3 N,N-Dimethylpropargylamin 
• 671-59-0 chloroacetone oxime 

Downstream Products

• 94467-30-8 Dimethyl-phenyl-ammonium-acetoxim-bromid 
• 95390-06-0 Dimethyl-phenyl-ammonium-acetoxim-iodid 

Relevant articles and documents

Supernucleophilic systems based on functionalized surfactants in the decomposition of 4-nitrophenyl esters derived from phosphorus and sulfur acids. III. Reactivity of mixed micellar systems based on tetraalkylammonium and imidazolium surfactants

Reactivity of mixed micellar systems based on the functionalized imidazolium and tetraalkylammonium surfactanats in the reaction of cleavage of 4-nitrophenyl ethyl ethylphosphonate was studied. Replacing of an imidazolium fragment in the detergent structure with a tetraalkylammonium one reveals decreasing the substrate solubilization efficiency. In the case of dimeric surfactants, the nucleophilicity of the oximate fragment is considerably (ca. 2 times) decreased thus additionally decreasing the rate of cleavage of the organophosphorus substarte. Therefore the nature of the cationic center in the head group may affect the extent of the observed micellar effects of functionalized surfactants.

Intermolecular retro-cope type hydroxylamination of alkynes with NH 2OH: (E-1-(1-hydroxycyclohexyl)ethanone oxime)

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