7539-61-9

Basic information

• Product Name: 3-(dipropan-2-ylamino)propan-1-ol
• CAS NO: 7539-61-9
• Molecular Formula: C₉H₂₁NO
• Molecular Weight: 159.2691
• Mol File: 7539-61-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 226.6°C at 760 mmHg
• Flash Point: 73.9°C
• Density: 0.872g/cm³
• Vapor Pressure: 0.016mmHg at 25°C
• Refractive Index: 1.448
• CAS DataBase Reference: 3-(dipropan-2-ylamino)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(dipropan-2-ylamino)propan-1-ol(7539-61-9)
• EPA Substance Registry System: 3-(dipropan-2-ylamino)propan-1-ol(7539-61-9)

Safety Data

• Hazardous Substances Data: 7539-61-9(Hazardous Substances Data)

Usage

General Description

3-(dipropan-2-ylamino)propan-1-ol is a chemical compound with the molecular formula C9H21NO. It is a tertiary amine with a hydroxyl group attached to the carbon chain. 3-(dipropan-2-ylamino)propan-1-ol is commonly used as a pharmaceutical intermediate and building block for the synthesis of various drugs. Its primary application is in the production of pharmaceuticals such as propranolol, an important beta-blocker used to treat high blood pressure, angina, and other cardiovascular conditions. Additionally, it can also be used as a reactant in organic synthesis for the preparation of other complex compounds. This chemical is typically handled and stored according to standard laboratory procedures and should be used with caution due to its potential for health hazards if handled improperly.

Upstream product

• 503-30-0 trimethylene oxide 
• 693-03-8 n-butyl magnesium bromide 
• 60-29-7 diethyl ether 
• 108-18-9 diisopropylamine 
• 627-30-5 1-chloro-3-hydroxypropane 
• 627-18-9 1-bromo-3-propanol 

Downstream Products

• 866723-81-1 2-[(3-diisopropylamino-propyl)-phenyl-phosphinoylmethyl]-isoindole-1,3-dione 
• 866723-72-0 [3-(aminomethyl-phenyl-phosphinoyl)-propyl]-diisopropyl-amine 
• 866723-78-6 (3-diisopropylamino-propyl)-phenyl-phosphinic acid ethyl ester 
• 866723-79-7 diisopropyl-(3-phenylphosphinoyl-propyl)-amine 

Relevant articles and documents

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LiBF4 in acetonitrile efficiently catalyzes the aminolysis of trimethylene oxide and 2-octyl oxetane under mild conditions (r.t. or 80 deg C) to give the corresponding γ-amino alcohols in very good yields.

Omega-quaternary ammonium alkyl esters and thioesters of acidic nonsteroidal antiinflammatory drugs

Quaternary ammonium alkyl esters and thioesters of acidic nonsteroidal anti-inflammatory drugs (NSAIDs) are disclosed. These esters and thioesters display the anti--inflammatory profile of the parent NSAIDs with greatly reduced gastrointestinal irritancy, providing a more favorable separation of therapeutic activity and toxicological side effects than the parent NSAIDs.