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5-(Isopropylamino)pentanol, with the molecular formula C8H19NO, is a versatile tertiary amine that features both an isopropyl group and a hydroxyl group. Its unique structure allows for a wide range of applications in the chemical and pharmaceutical industries.

40447-21-0

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40447-21-0 Usage

Uses

Used in Pharmaceutical Synthesis:
5-(Isopropylamino)pentanol is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 5-(Isopropylamino)pentanol serves as a key component in the synthesis of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used as a Solvent in Chemical Reactions:
5-(Isopropylamino)pentanol is utilized as a solvent in numerous chemical reactions, facilitating processes and improving the efficiency of various industrial applications.
Used in Surfactant Production:
As a chemical intermediate, 5-(Isopropylamino)pentanol plays a crucial role in the production of surfactants, which are essential for the manufacturing of detergents, cleaners, and other consumer products.
Used in Other Organic Compounds Synthesis:
5-(Isopropylamino)pentanol is also employed as a building block in the synthesis of other organic compounds, further expanding its utility across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 40447-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40447-21:
(7*4)+(6*0)+(5*4)+(4*4)+(3*7)+(2*2)+(1*1)=90
90 % 10 = 0
So 40447-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H19NO/c1-8(2)9-6-4-3-5-7-10/h8-10H,3-7H2,1-2H3

40447-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(propan-2-ylamino)pentan-1-ol

1.2 Other means of identification

Product number -
Other names N-isopropyl-5-aminopentanol

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:40447-21-0 SDS

40447-21-0Downstream Products

40447-21-0Relevant academic research and scientific papers

Triazolo[4,5-f]quinolines. Part VI. Synthesis and evaluation of 9-aminoalkyl(aryl)-2-methyl-2H-[4,5-f]quinolines as anticancer agents. Preliminary results of in vitro screening

Sanna,Sequi,Pagletti

, p. 47 - 54 (2007/10/02)

9-Aminoalkyl(aryl)-2-methyl-2H-triazolo[4,5-f]quinolines were prepared in order to evaluate their in vitro antitumor activity. Some members of this series exbibited both cell selectivity and tumor growth inhibition activity at concentrations between 10su

Quaternary alkynoxymethyl amines

-

, (2008/06/13)

This invention relates to quaternaries of alkynoxymethyl amines and uses thereof. These may be summarized by the following formulae: STR1 where R and R' are substituted groups such as alkyl, aryl, etc.; R'" is an acetylenic group; and X is an anion; and STR2 where R and R'" having the same meaning as in (1) and Z is a bridging group, preferably hydrocarbon such as alkylene, alkinylene, alkenylene, arylene, etc.

Microbiocidal quaternaries of halogen derivatives of alkynoxymethyl amines

-

, (2008/06/13)

This invention relates to quaternaries of halogen derivatives of alkynoxymethyl amines and uses thereof. These may be summarized by the following formulae: STR1 where R and R' are substituted groups such as alkyl, aryl, etc.; R" is an alkylidene group; and X is halogen and A is an anion; and STR2 where R, R' and R" having the same meaning as in (1) and Z is a bridging group, preferably hydrocarbon such as alkylene, alkinylene, alkenylene, arylene, etc.

Halogen derivatives of alkynoxymethyl amines

-

, (2008/06/13)

This invention relates to halogen derivatives of alkynoxymethylamines and to uses thereof. The present invention may be ideally illustrated by the following equation: where R is a substituted group, preferably hydrocarbon, such as alkyl, cycloalkyl, aryl, etc., R' is hydrocarbon, preferably alkylene, and where X is halogen.

Alkynoxymethyl amines

-

, (2008/06/13)

This invention relates to alkynoxymethyl amines, to methods of preparing them, and uses thereof, particularly as corrosion inhibitors. These compounds are prepared by reacting an amine, such as RNH2, with an aldehyde, such as formaldehyde, and an alkynol, such as propargyl alcohol, to yield compounds of the formula where R is a substituted group, preferably alkyl, cycloalkyl, aryl, etc., and R' is an acetylenic alcohol moiety.

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