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6272-74-8

6272-74-8

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6272-74-8 Usage

Uses

Pharmaceutic aid (surfactant).

Check Digit Verification of cas no

The CAS Registry Mumber 6272-74-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6272-74:
(6*6)+(5*2)+(4*7)+(3*2)+(2*7)+(1*4)=98
98 % 10 = 8
So 6272-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H34N2O3.ClH/c1-2-3-4-5-6-7-8-9-11-14-21(25)26-18-15-22-20(24)19-23-16-12-10-13-17-23;/h10,12-13,16-17H,2-9,11,14-15,18-19H2,1H3;1H

6272-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl dodecanoate,chloride

1.2 Other means of identification

Product number -
Other names Emcol E-607

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:6272-74-8 SDS

6272-74-8Synthetic route

2-(2-chloroacetylamino)ethyl dodecanoate
873009-81-5

2-(2-chloroacetylamino)ethyl dodecanoate

pyridine
110-86-1

pyridine

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride
6272-74-8

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride

Conditions
ConditionsYield
at 20℃;87%
n-dodecanoyl chloride
112-16-3

n-dodecanoyl chloride

2-chloro-N-2-hydroxyethylacetamide
6320-16-7

2-chloro-N-2-hydroxyethylacetamide

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride
6272-74-8

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride

Conditions
ConditionsYield
unter vermindertem Druck und Erwaermen des Reaktionsprodukts mit Pyridin;
lauric acid
143-07-7

lauric acid

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride
6272-74-8

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 95 percent / Lipozyme RM 1 M / acetone / 24 h / 20 °C / Enzymatic reaction
2: 87 percent / 20 °C
View Scheme
ethyl laurate
106-33-2

ethyl laurate

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride
6272-74-8

1-[(2-dodecanoyloxyethylcarbamoyl)methyl]pyridinium chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 75 percent / Lipozyme RM 1 M / acetone / 24 h / 20 °C / Enzymatic reaction
2: 87 percent / 20 °C
View Scheme

6272-74-8Downstream Products

6272-74-8Relevant articles and documents

An efficient chemoenzymatic synthesis of the bactericide lapyrium chloride

Rustoy, Eduardo M.,Baldessari, Alicia

, p. 4628 - 4632 (2007/10/03)

An efficient route for large-scale preparation of lapyrium chloride, a broad-spectrum antimicrobial surfactant, was developed from chloroacetic acid in four steps, three of them enzymatic. Due to the chemoselective behavior of the biocatalysts, lapyrium chloride was obtained in a high degree of purity and yield, from mild reaction conditions and following a low environmental impact methodology. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.

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