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Piperidine, 1-(3-methylbutyl)-, also known as 1-(3-methylbutyl)piperidine or 1-isopentylpiperidine, is an organic compound with the chemical formula C10H21N. It is a derivative of piperidine, a heterocyclic amine with a six-membered ring containing one nitrogen atom. The 3-methylbutyl group is attached to the nitrogen atom, making it a substituted piperidine. Piperidine, 1-(3-methylbutyl)- is a colorless liquid with a pungent odor and is soluble in organic solvents. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications and reactivity, it is important to handle 1-(3-methylbutyl)piperidine with care, as it may have toxicological properties and should be stored away from heat and open flames.

4462-09-3

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4462-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4462-09-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4462-09:
(6*4)+(5*4)+(4*6)+(3*2)+(2*0)+(1*9)=83
83 % 10 = 3
So 4462-09-3 is a valid CAS Registry Number.

4462-09-3SDS

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 N-(3-methylbutyl)piperidine

1.2 Other means of identification

Product number -
Other names Piperidine, 1-(3-methylbutyl)-

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:4462-09-3 SDS

4462-09-3Relevant academic research and scientific papers

Synthesis and properties of pentane amino derivatives

Talybov,Mamedbeili,Abbasov,Kochetkov

experimental part, p. 2455 - 2459 (2011/04/16)

Synthesis of pentane amino derivatives by the reaction of the corresponding amines with 1-bromopentanes of n-and iso-structure by environmentally safe methods in water medium was carried out. The structure of the compounds obtained was confirmed by elemental analysis, IR, 1H and 13C NMR spectroscopy. The products synthesized were tested as reagents for the suppression of growth of the sulfate-reducing bacteria and as the anticorrosive substances. It was found that they are effective bactericides for the sulfate-reducing bacteria and exhibit high anticorrosive properties. Pleiades Publishing, Ltd., 2010.

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