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82394-21-6

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82394-21-6 Usage

Chemical Category

Piperazine derivatives

Composition

Piperazine ring with two dodecyl groups attached at the 1 and 4 positions

Primary Use

Corrosion inhibitor in metalworking fluids

Specific Application

Protection of aluminum alloys

Additional Use

Additive in lubricants

Lubricant Function

Acts as an antioxidant and anti-wear agent

Potential Applications

Pharmaceutical field

Potential Applications

Surfactant in cleaning products

Nature

Amphiphilic

Role

Vital in various industrial processes

Development

Potential for further development in diverse fields

Check Digit Verification of cas no

The CAS Registry Mumber 82394-21-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,9 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82394-21:
(7*8)+(6*2)+(5*3)+(4*9)+(3*4)+(2*2)+(1*1)=136
136 % 10 = 6
So 82394-21-6 is a valid CAS Registry Number.

82394-21-6SDS

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 1,4-didodecylpiperazine

1.2 Other means of identification

Product number -
Other names 1,4-didodecyl-piperazine

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:82394-21-6 SDS

82394-21-6Downstream Products

82394-21-6Relevant articles and documents

Rhodium-Catalyzed Bis-Hydroaminomethylation of Linear Aliphatic Alkenes with Piperazine

Seidensticker, Thomas,Vosberg, Jonas M.,Ostrowski, Karoline A.,Vorholt, Andreas J.

supporting information, p. 610 - 621 (2016/02/27)

An efficient protocol was developed to prepare a series of dialkylpiperazines via Rh-catalyzed bis-hydroaminomethylation of linear aliphatic alkenes with piperazine. The well-known Rh/Biphephos catalytic system was applied, yielding the desired dialkylpiperazines within six tandem catalytic steps, already at low catalyst loadings of 0.1 mol%. For the model alkene 1-octene, good yields and linearities of 80% and 77:23, respectively, were achieved under optimized conditions. Influences on the catalytic system regarding n/iso ratio, possible side reactions and the reaction path are discussed on the basis of yield vs. time plots and parameter optimization. With the developed general protocol, other linear, functionalized and branched substrates were effectively transformed to the corresponding linear N,N-disubstituted piperazines.

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