Welcome to LookChem.com Sign In|Join Free
  • or
3-(dipropan-2-ylamino)propan-1-ol, a chemical compound with the molecular formula C9H21NO, is a tertiary amine featuring a hydroxyl group attached to the carbon chain. It is primarily recognized for its role as a pharmaceutical intermediate and a building block in the synthesis of various drugs.

7539-61-9

Post Buying Request

7539-61-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7539-61-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(dipropan-2-ylamino)propan-1-ol is used as a pharmaceutical intermediate for the production of drugs such as propranolol, a crucial beta-blocker utilized in the treatment of high blood pressure, angina, and other cardiovascular conditions.
Used in Organic Synthesis:
In the realm of organic synthesis, 3-(dipropan-2-ylamino)propan-1-ol serves as a reactant for the preparation of other complex compounds, contributing to the development of novel chemical entities and materials.
Safety and Handling:
This chemical should be handled and stored according to standard laboratory procedures, and caution is advised due to its potential health hazards if mismanaged.

Check Digit Verification of cas no

The CAS Registry Mumber 7539-61-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7539-61:
(6*7)+(5*5)+(4*3)+(3*9)+(2*6)+(1*1)=119
119 % 10 = 9
So 7539-61-9 is a valid CAS Registry Number.

7539-61-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[di(propan-2-yl)amino]propan-1-ol

1.2 Other means of identification

Product number -
Other names 3-Diisopropylamino-propylalkohol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7539-61-9 SDS

7539-61-9Relevant academic research and scientific papers

A versatile and recyclable molecularly imprinted polymer as an oxidative catalyst of sulfur derivatives: A new possible method for mustard gas and v nerve agent decontamination

Mohamed, Sophie,Balieu, Sébastien,Petit, Emilie,Galas, Ludovic,Schapman, Damien,Hardouin, Julie,Baati, Rachid,Estour, Fran?ois

supporting information, p. 13243 - 13246 (2019/11/16)

A molecularly imprinted polymer containing a porphyrin unit was developed as a biomimetic heterogenous catalyst for the oxidation of sulfur derivatives. Its catalytic efficiency under mild conditions and its easy recovery represent a great asset for the design of new decontamination tools for yperite and VX.

Diesters of carbonic acid endowed with antiviral and anti-inflammatory activity

-

, (2008/06/13)

Diesters of carbonic acid disubstituted with primary, secondary or tertiary amine groups, pharmaceutically acceptable salts thereof, and their use as antiviral and inti-inflammatory agents.

Mild LIBF4-Promoted Aminolysis of Oxetanes

Chini, Marco,Crotti, Paolo,Favero, Lucilla,Macchia, Franco

, p. 761 - 764 (2007/10/02)

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.

Compounds for the treatment of urinary incontinence

-

, (2008/06/13)

The invention concerns compounds having the formula I STR1 wherein Ar is a phenyl or benzyl group which is optionally substituted with hydroxy or alkoxy;R 1 is hydrogen, lower alkyl, lower alkoxy, hydroxy;R 2 is hydrogen, lower alkyl;R 3 is NR 4 R 5, whereinR 4 and R 5 which can be the same or different, are lower alkyl, or wherein R 4 and R 5, when taken together, form a ring with the nitrogen atom, whereby said ring optionally is substituted with lower alkyl;n is 0 or 1;m is 2 or 3 andtheir salts with physiologically acceptable acids and when the compounds can be in form of optical isomers, the racemic mixture and the individual isomers, for the treatment of disorders of the urinary bladder.

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

-

, (2008/06/13)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7539-61-9