99931-16-5

Basic information

• Product Name: 2-Propanol, 1-[bis(phenylmethyl)amino]-3-chloro-
• CAS NO: 99931-16-5
• Molecular Formula: C17H20ClNO
• Molecular Weight: 289.805
• Mol File: 99931-16-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-Propanol, 1-[bis(phenylmethyl)amino]-3-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanol, 1-[bis(phenylmethyl)amino]-3-chloro-(99931-16-5)
• EPA Substance Registry System: 2-Propanol, 1-[bis(phenylmethyl)amino]-3-chloro-(99931-16-5)

Safety Data

• Hazardous Substances Data: 99931-16-5(Hazardous Substances Data)

Upstream product

• 106-89-8 epichlorohydrin 
• 103-49-1 dibenzylamine 
• 88285-82-9 N,N-bis(phenylmethyl)-2-oxiranemethanamine 

Downstream Products

• 88285-82-9 N,N-bis(phenylmethyl)-2-oxiranemethanamine 

Relevant articles and documents

Experimental and theoretical research on a new corrosion inhibitor for effective oil and gas acidification

A new dibenzylamine-quinoline derivative (DEEQ) was synthesized and investigated as a corrosion inhibitor for mild steel in 15% HCl solution in various ways, including via weight loss measurements, contact angle measurements, electrochemical measurements

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Amino functional poly(ethylene glycol) copolymers via protected amino glycidol

The synthesis of poly (ethylene glycol) (PEG) copolymers with multiple amino functionalities within the chain is described, relying on an epoxide comonomer bearing a protected amino group. N,Ndibenzyl amino glycidol (DBAG) and ethylene oxide (EO) were copolymerized via anionic polymerization, leading to well-defined polymers with varied comonomer content and low polydispersities (Mw/Mn in the range of 1.1 to 1.2). Subsequent hydrogenolysis with Pearlman's catalyst afforded polyethylene glycol-coamino glycerols (PEG-coPAG) with a precisely adjusted number of randomly incorporated amino groups in the range of 2-15%. For the first time, the kinetics of an. EO copolymerizations have has been directly monitored by 1H NMR spectroscopy in real time. Monomer consumption and compositional drift in monomer feed have been studied for various reaction temperatures, revealing a slightly tapered yet random DBAG distribution in the copolymers. The random structure of the copolymers was confirmed by detailed 13C NMR characterization of EO- and DBAG-centered triad sequence distribution and DSC measurements.