24417-04-7

Basic information

• Product Name: 2-(ethylamino)propan-1-ol
• Synonyms: 2-(ethylamino)propan-1-ol;2-(ethylamino)-1-propanol(SALTDATA: FREE);2-(ethylamino)-1-propanol
• CAS NO: 24417-04-7
• Molecular Formula: C5H13NO
• Molecular Weight: 103.16282
• Mol File: 24417-04-7.mol

Chemical Properties

• Boiling Point: 170.418°C at 760 mmHg
• Flash Point: 70.331°C
• Appearance: /
• Density: 0.876g/cm³
• Vapor Pressure: 0.472mmHg at 25°C
• Refractive Index: 1.428
• Storage Temp.: 2-8°C(protect from light)
• PKA: 15.08±0.10(Predicted)
• CAS DataBase Reference: 2-(ethylamino)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(ethylamino)propan-1-ol(24417-04-7)
• EPA Substance Registry System: 2-(ethylamino)propan-1-ol(24417-04-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 24417-04-7(Hazardous Substances Data)

Usage

Uses

Used in Personal Care Products:
2-(ethylamino)propan-1-ol is used as a surfactant for its ability to reduce surface tension, allowing for easier mixing with other ingredients and improving the texture and performance of personal care products.
Used in Cleaning Agents:
In the cleaning industry, 2-(ethylamino)propan-1-ol is used as a surfactant to enhance the cleaning power of agents by reducing the surface tension of water, enabling it to mix more effectively with dirt and grime for easier removal.
Used in Metalworking Fluids:
2-(ethylamino)propan-1-ol serves as a surfactant in metalworking fluids, improving the fluid's ability to lubricate and cool during manufacturing processes, as well as facilitating the dispersion of the fluid for more even application.
Used as a Corrosion Inhibitor:
2-(ethylamino)propan-1-ol is used to protect metal surfaces from corrosion, as its chemical properties can form a protective layer that prevents oxidation and other corrosive processes.
Used as a Solvent in Chemical Reactions:
In chemical processes, 2-(ethylamino)propan-1-ol acts as a solvent, providing a medium for reactions to occur, and potentially influencing the rate and yield of the reactions due to its ability to dissolve a variety of substances.

InChI:InChI=1/C5H13NO/c1-3-6-5(2)4-7/h5-7H,3-4H2,1-2H3

Upstream product

• 6159-23-5 (R,S)-2,4-dimethyl-2-oxazoline 
• 6168-72-5 2-Amino-1-propanol 
• 108-24-7 acetic anhydride 

Downstream Products

• 52260-14-7 N-Ethyl-N-2-propenyl-benzolsulfonamid 
• 52260-13-6 N-Ethyl-N-2-propenyl-p-toluolsulfonamid 
• 53119-82-7 N-Ethyl-N-(3-p-toluolsulfonyloxy-2-propyl)-p-toluolsulfonamid 

Relevant articles and documents

Further Studies on a Site-specific Hydrogen Transfer Observed in Electron Capture Negative Ion Chemical Ionization Mass Spectrometry of Hydroxyamine Pentafluoropropionate Derivatives

Further studies have demonstrated that the site-specific hydrogen transfer process involved in the formation of the m/z 145 anion of β-hydroxyamine pentafluoropropionate (PFP) derivatives observed under electron capture negative ion chemical ionization conditions occurs when the two functional groups are separated by up to five carbon atoms.Deuterium labelling has established that the site specificity, transfer of a hydrogen atom from the carbon adjacent to nitrogen to the OPFP group, is maintained in 4-amino-butan-1-ol-N,O-(PFP)2.The corresponding PFP derivatives of the N-methylaminoalkanol- (PFP)2 derivatives lack the m/z 145 species with m/z 163, -, being the base anion.Substitution of alkyl groups on the carbon adjacent to oxygen results in a diminution of the ion intensity at m/z 145 with a marked increase in the intensity of m/z 144.The formation of the m/z 145 and 144 anions is proposed to proceed through the intervention of a fluoride ion-molecule complex as outlined in Scheme 1 with the product ion distribution dependent on which of the two pathways is preferred.