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538-71-6

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538-71-6 Usage

Description

Domiphen bromide, also known as Domiphen, is a quaternary ammonium compound and cationic surfactant with potent antimicrobial properties. It is effective against a range of bacteria, including A. viscosus, A. naeslundii, S. mutans, E. coli, and L. monocytogenes, as well as inhibiting the growth and spore germination of C. neoformans yeast. Additionally, it has the ability to inhibit the human-ether-a-go-go-related gene (hERG) channel, making it a versatile compound with various applications across different industries.

Uses

Used in Synthetic Chemistry:
Domiphen bromide is used as a phase transfer catalyst, facilitating reactions in synthetic chemistry by promoting the transfer of reactants between different phases, thus enhancing the efficiency and yield of chemical processes.
Used in Industrial Applications:
As a cationic surfactant with antimicrobial properties, Domiphen bromide is utilized in various industrial applications, such as in the formulation of antiseptics, disinfectants, and biocides. Its broad-spectrum activity against bacteria and yeast makes it a valuable component in maintaining cleanliness and preventing the spread of microorganisms in industrial settings.
Used in Agricultural Applications:
In agriculture, Domiphen bromide is employed as a biocide to control the growth of harmful microorganisms that can negatively impact crop yields and quality. Its antimicrobial activity helps protect plants from diseases and pests, contributing to a more sustainable and efficient agricultural system.
Used in Veterinary Applications:
Domiphen bromide is also used in the veterinary industry as an antiseptic and disinfectant, helping to maintain hygiene and prevent the spread of infections in animals. Its effectiveness against a wide range of bacteria and yeast makes it a valuable tool in ensuring the health and well-being of animals in veterinary care.
Used in Clinical Applications:
In the clinical setting, Domiphen bromide is used as an active pharmaceutical ingredient, leveraging its antimicrobial properties to treat various infections. Its ability to inhibit the hERG channel also makes it a potential candidate for further research and development in the pharmaceutical industry, with the potential to contribute to the treatment of various medical conditions.

Originator

Bradosol,Ciba,US,1958

Manufacturing Process

7 parts of β-phenoxyethyl-dimethylamine are heated for 2 hours on the boiling water-bath with 11 parts of dodecyl bromide. A good yield of β-phenoxy-ethyldimethyl-dodecyl-ammonium bromide is obtained which, after recrystallization from acetone, melts at 112°C. It is a white crystalline powder which dissolves easily in water to give a neutral reaction.

Safety Profile

Poison by intraperitoneal and intravenous routes. hfutauon data reported. When heated to decomposiuon it emits very toxic fumes of NOx, NH3, and Br-. See also BROMIDES.

Check Digit Verification of cas no

The CAS Registry Mumber 538-71-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 538-71:
(5*5)+(4*3)+(3*8)+(2*7)+(1*1)=76
76 % 10 = 6
So 538-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H40NO.BrH/c1-4-5-6-7-8-9-10-11-12-16-19-23(2,3)20-21-24-22-17-14-13-15-18-22;/h13-15,17-18H,4-12,16,19-21H2,1-3H3;1H/q+1;/p-1

538-71-6 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L12930)  Domiphen bromide, 97%   

  • 538-71-6

  • 25g

  • 314.0CNY

  • Detail
  • Alfa Aesar

  • (L12930)  Domiphen bromide, 97%   

  • 538-71-6

  • 100g

  • 896.0CNY

  • Detail
  • Aldrich

  • (247480)  Domiphenbromide  97%

  • 538-71-6

  • 247480-25G

  • 468.00CNY

  • Detail

538-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Domiphen bromide

1.2 Other means of identification

Product number -
Other names Dodecyldimethyl-2-Phenoxyethylammonium Bromide

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:538-71-6 SDS

538-71-6Synthetic route

dimethyl(2-phenoxyethyl)amine
13468-02-5

dimethyl(2-phenoxyethyl)amine

1-dodecylbromide
143-15-7

1-dodecylbromide

domiphen brominde
538-71-6

domiphen brominde

n-Dodecylamine
124-22-1

n-Dodecylamine

phenoxyethyl bromide
589-10-6

phenoxyethyl bromide

domiphen brominde
538-71-6

domiphen brominde

Conditions
ConditionsYield
With methyl bromide; formaldehyd; formic acid
N,N-dimethylaminododecane
112-18-5

N,N-dimethylaminododecane

phenoxyethyl bromide
589-10-6

phenoxyethyl bromide

domiphen brominde
538-71-6

domiphen brominde

Conditions
ConditionsYield
With ethyl acetate
With acetone
With water
domiphen brominde
538-71-6

domiphen brominde

3,6-dichloro-2-methoxybenzoate sodium salt
1918-00-9

3,6-dichloro-2-methoxybenzoate sodium salt

dodecyldimethylphenoxyethylammonium 3,6-dichloro-2-methoxybenzoate

dodecyldimethylphenoxyethylammonium 3,6-dichloro-2-methoxybenzoate

Conditions
ConditionsYield
In water99.5%
(R)-Mecoprop
16484-77-8

(R)-Mecoprop

domiphen brominde
538-71-6

domiphen brominde

domiphen (+)-(R)-2-(4-chloro-2-methylphenoxy)propionate
1354725-99-7

domiphen (+)-(R)-2-(4-chloro-2-methylphenoxy)propionate

Conditions
ConditionsYield
Stage #1: (R)-Mecoprop With potassium hydroxide In water at 39.84℃;
Stage #2: domiphen brominde In water for 24h;
99%
MCPA
94-74-6

MCPA

domiphen brominde
538-71-6

domiphen brominde

domiphen (4-chloro-2-methylphenoxy)acetate
1082249-07-7

domiphen (4-chloro-2-methylphenoxy)acetate

Conditions
ConditionsYield
With sodium hydroxide In water for 2h;98%
domiphen brominde
538-71-6

domiphen brominde

L-proline
147-85-3

L-proline

C22H40NO(1+)*C5H8NO2(1-)

C22H40NO(1+)*C5H8NO2(1-)

Conditions
ConditionsYield
With potassium hydroxide In water at 59.84℃; for 12h;92%
N-(phosphonemethyl)glycine
1071-83-6

N-(phosphonemethyl)glycine

domiphen brominde
538-71-6

domiphen brominde

bis(N,N-dimethyl-N-dodecyl-N-phenoxyethylammonium) glyphosate

bis(N,N-dimethyl-N-dodecyl-N-phenoxyethylammonium) glyphosate

Conditions
ConditionsYield
Stage #1: domiphen brominde With potassium hydroxide In 1,4-dioxane at 25℃; for 6h;
Stage #2: N-(phosphonemethyl)glycine In 1,4-dioxane at 25℃; for 6h;
92%

538-71-6Relevant articles and documents

Dentifrice containing a poly(hydroxypropyl ether) non-ionic surfactant and a specified cationic polymer

-

, (2008/06/13)

Dentifrice containing, in combination, (A) a poly(hydroxypropyl ether) nonionic surfactant, and (B) a cationic polymer selected from the group consisting of (i) a vinylpyrrolidone/dialkylaminoalkyl or -hydroxyalkyl acrylate or methacrylate, quaternized or nonquaternized and (ii) a cationic polysaccharide. This dentifrice is characterized by good foamability, pleasant taste and it does not attack the buccal mucosae and the gums.

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