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Didecyl dimethyl ammonium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7173-51-5

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7173-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7173-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7173-51:
(6*7)+(5*1)+(4*7)+(3*3)+(2*5)+(1*1)=95
95 % 10 = 5
So 7173-51-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H48N.ClH/c1-5-7-9-11-13-15-17-19-21-23(3,4)22-20-18-16-14-12-10-8-6-2;/h5-22H2,1-4H3;1H/q+1;/p-1

7173-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Didecyl Dimethyl Ammonium Chloride

1.2 Other means of identification

Product number -
Other names didecyl(dimethyl)azanium,chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Surface active agents
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:7173-51-5 SDS

7173-51-5Synthetic route

1-bromo dodecane
112-29-8

1-bromo dodecane

N,N-dimethyldecylamine
1120-24-7

N,N-dimethyldecylamine

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
Stage #1: 1-bromo dodecane; N,N-dimethyldecylamine
Stage #2: With hydrogenchloride In water
95%
methylene chloride
74-87-3

methylene chloride

N-methyldidecylamine
7396-58-9

N-methyldidecylamine

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
With ethyl acetate at 80℃;
With sodium carbonate In isopropyl alcohol at 80 - 90℃; under 2250.23 - 3750.38 Torr; for 4h; Autoclave;340 g
decyl chloride
1002-69-3

decyl chloride

N,N-dimethyldecylamine
1120-24-7

N,N-dimethyldecylamine

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
In ethanol
In methanol at 65 - 142℃; Conversion of starting material;
1-bromo dodecane
112-29-8

1-bromo dodecane

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile / 12 h / 90 °C
2: hydroxide ion-exchange resin
3: hydrogenchloride / water / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1.1: acetonitrile / 12 h / 90 °C
2.1: water / Alkaline conditions
2.2: Inert atmosphere
View Scheme
N,N-dimethyldecylamine
1120-24-7

N,N-dimethyldecylamine

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile / 12 h / 90 °C
2: hydroxide ion-exchange resin
3: hydrogenchloride / water / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1.1: acetonitrile / 12 h / 90 °C
2.1: water / Alkaline conditions
2.2: Inert atmosphere
View Scheme
(bisdecyl)(dimethyl)ammonium hydroxide

(bisdecyl)(dimethyl)ammonium hydroxide

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
With hydrogenchloride In water Inert atmosphere;
N,N-didecyl-N,N-dimethylammonium bromide
2390-68-3

N,N-didecyl-N,N-dimethylammonium bromide

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Conditions
ConditionsYield
Stage #1: N,N-didecyl-N,N-dimethylammonium bromide In water Alkaline conditions;
Stage #2: With hydrogenchloride In water Inert atmosphere;
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

diclofenac sodium
15307-79-6

diclofenac sodium

diclofenac didecyldimethylammonium salt
934544-42-0

diclofenac didecyldimethylammonium salt

Conditions
ConditionsYield
In water at 20℃; for 0.5h; Product distribution / selectivity;100%
triclosan
3380-34-5

triclosan

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium-triclosan complex

didecyldimethylammonium-triclosan complex

Conditions
ConditionsYield
Stage #1: triclosan With sodium hydroxide In water at 60℃;
Stage #2: didecyldimethylammonium chloride In water at 80℃; for 2h;
100%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

saccharin sodium salt
128-44-9

saccharin sodium salt

didecyldimethylammonium saccharinate
934544-24-8

didecyldimethylammonium saccharinate

Conditions
ConditionsYield
In water at 60℃; for 1h;98%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium mandelate
934544-48-6

didecyldimethylammonium mandelate

Conditions
ConditionsYield
With sodium hydroxide In water at 50℃; for 2h;96%
With potassium hydroxide In water at 60℃; for 5h;92%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium 1,2,4-triazolate
1256751-71-9

didecyldimethylammonium 1,2,4-triazolate

Conditions
ConditionsYield
In methanol at 20℃; Alkaline conditions;96%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

toluene-4-sulfonic acid
104-15-4

toluene-4-sulfonic acid

Didecyldimethylammonium p-toluenesulfonate
132781-87-4

Didecyldimethylammonium p-toluenesulfonate

Conditions
ConditionsYield
With sodium hydroxide In water at 40℃; for 2h; Heating / reflux;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Naprelan
26159-34-2

Naprelan

didecyldimethylammonium (S)-6-methoxy-α-methyl-2-naphthaleneacetate
934544-44-2

didecyldimethylammonium (S)-6-methoxy-α-methyl-2-naphthaleneacetate

Conditions
ConditionsYield
In water at 20℃; for 1h;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

sodium salicylate
54-21-7

sodium salicylate

didecyldimethylammonium salicylate
934544-38-4

didecyldimethylammonium salicylate

Conditions
ConditionsYield
In water at 40℃; for 1h;95%
MCPA
94-74-6

MCPA

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium (4-chloro-2-methylphenoxy)-acetate
1082249-04-4

didecyldimethylammonium (4-chloro-2-methylphenoxy)-acetate

Conditions
ConditionsYield
Stage #1: MCPA With sodium hydroxide In water at 50℃;
Stage #2: didecyldimethylammonium chloride In water at 20℃; for 0.5h;
95%
With sodium hydroxide In water at 69.84℃; for 24h;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

L-proline
147-85-3

L-proline

didecyldimethylammonium L-prolinate
1287759-29-8

didecyldimethylammonium L-prolinate

Conditions
ConditionsYield
With potassium hydroxide In water at 60℃; for 5h;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

2-methyl-4-nitro-1H-imidazole
696-23-1

2-methyl-4-nitro-1H-imidazole

didecyldimethylammonium 2-methyl-4-nitroimidazolate
1256751-77-5

didecyldimethylammonium 2-methyl-4-nitroimidazolate

Conditions
ConditionsYield
In methanol at 20℃; Alkaline conditions;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

sodium cyclamate
139-05-9

sodium cyclamate

didecyldimethylammonium cyclamate
1403558-45-1

didecyldimethylammonium cyclamate

Conditions
ConditionsYield
In water at 20℃; for 24h;95%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

potassium acesulfamate

potassium acesulfamate

didecyldimethylammonium acesulfamate
934544-25-9

didecyldimethylammonium acesulfamate

Conditions
ConditionsYield
In water at 60℃; for 1h;94%
D-Lactic acid
10326-41-7

D-Lactic acid

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium L-lactate
1308889-80-6

didecyldimethylammonium L-lactate

Conditions
ConditionsYield
Stage #1: D-Lactic acid With potassium hydroxide In water Reflux;
Stage #2: didecyldimethylammonium chloride In water at 20℃; for 5h;
94%
(R)-Mecoprop
16484-77-8

(R)-Mecoprop

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium (+)-(R)-2-(4-chloro-2-methylphenoxy)propionate
1354725-98-6

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

Conditions
ConditionsYield
Stage #1: (R)-Mecoprop With potassium hydroxide In water at 69.84℃;
Stage #2: didecyldimethylammonium chloride In water for 24h;
94%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

2-chloro-N-((4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl)benzenesulfonamide potassium

2-chloro-N-((4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl)benzenesulfonamide potassium

didecyldimethylammonium chlorsulfuron

didecyldimethylammonium chlorsulfuron

Conditions
ConditionsYield
In methanol at 40℃; for 1h;94%
2,6-dinitro-3,4-dimethylphenol
4097-61-4

2,6-dinitro-3,4-dimethylphenol

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

dimethyl sulfate
77-78-1

dimethyl sulfate

3,4-dimethyl-2,6-dinitroanisole
160754-06-3

3,4-dimethyl-2,6-dinitroanisole

Conditions
ConditionsYield
With sodium carbonate In water; 1,2-dichloro-ethane93.9%
With sodium carbonate In water; 1,2-dichloro-ethane93.9%
1,2,3-Benzotriazole
95-14-7

1,2,3-Benzotriazole

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium benzotriazolate
1256751-67-3

didecyldimethylammonium benzotriazolate

Conditions
ConditionsYield
In methanol at 20℃; Alkaline conditions;92%
methyl 4-iodo-2-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl]amino]sulfonyl]benzoate sodium salt
144550-36-7

methyl 4-iodo-2-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl]amino]sulfonyl]benzoate sodium salt

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium ((5-iodo-2-(methoxycarbonyl)phenyl)sulfonyl)((4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl)amidate

didecyldimethylammonium ((5-iodo-2-(methoxycarbonyl)phenyl)sulfonyl)((4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl)amidate

Conditions
ConditionsYield
In water at 40℃;92%
1H-4(5)-nitroimidazole
3034-38-6

1H-4(5)-nitroimidazole

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium 4-nitroimidazolate
1256751-74-2

didecyldimethylammonium 4-nitroimidazolate

Conditions
ConditionsYield
In methanol at 20℃; Alkaline conditions;91%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

aspirin
50-78-2

aspirin

didecyldimethylammonium 2-acetoxybenzoate
934544-49-7

didecyldimethylammonium 2-acetoxybenzoate

Conditions
ConditionsYield
With sodium hydroxide In water at 60℃; for 2h;90%
sodium salt of 4-amino-4-deoxypteroic acid
100929-45-1

sodium salt of 4-amino-4-deoxypteroic acid

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium N-[4-[[(2-amino-1,4-dihydro-4-oxo-6-pteridinyl)methyl]amino]benzoy]-L-glutamate
934544-43-1

didecyldimethylammonium N-[4-[[(2-amino-1,4-dihydro-4-oxo-6-pteridinyl)methyl]amino]benzoy]-L-glutamate

Conditions
ConditionsYield
In water at 20℃; for 0.5h;90%
LACTIC ACID
849585-22-4

LACTIC ACID

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium D,L-lactate
190782-63-9

didecyldimethylammonium D,L-lactate

Conditions
ConditionsYield
Stage #1: LACTIC ACID With potassium hydroxide In water Reflux;
Stage #2: didecyldimethylammonium chloride In water at 20℃; for 5h;
90%
(S)-Mandelic acid
17199-29-0

(S)-Mandelic acid

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium (S)-(+)-mandelate
1287759-28-7

didecyldimethylammonium (S)-(+)-mandelate

Conditions
ConditionsYield
With potassium hydroxide In water at 60℃; for 5h;90%
didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

sodium dimethyldithiocarbamate
128-04-1

sodium dimethyldithiocarbamate

didecyldimethylammonium dimethyldithiocarbamate complex
126813-76-1

didecyldimethylammonium dimethyldithiocarbamate complex

Conditions
ConditionsYield
In water90%
3,6-dichloro-O-anisic acid
1918-00-9

3,6-dichloro-O-anisic acid

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium 3,6-dichloro-2-methoxybenzoate
1354726-11-6

didecyldimethylammonium 3,6-dichloro-2-methoxybenzoate

Conditions
ConditionsYield
Stage #1: 3,6-dichloro-O-anisic acid With sodium hydroxide In water at 50℃;
Stage #2: didecyldimethylammonium chloride In water; isopropyl alcohol for 24h;
90%
(R)-Mandelic Acid
611-71-2

(R)-Mandelic Acid

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

didecyldimethylammonium (R)-(-)-mandelate
1287759-27-6

didecyldimethylammonium (R)-(-)-mandelate

Conditions
ConditionsYield
With potassium hydroxide In water at 60℃; for 5h;86%
sodium benzoate
532-32-1

sodium benzoate

didecyldimethylammonium chloride
7173-51-5

didecyldimethylammonium chloride

Didecyldimethylammonium Benzoate
934544-46-4

Didecyldimethylammonium Benzoate

Conditions
ConditionsYield
In water at 80℃; for 7h;85%

7173-51-5Relevant academic research and scientific papers

Supramolecular effects on the antifungal activity of cyclodextrin/di-n- decyldimethylammonium chloride mixtures

Leclercq, Lo?c,Lubart, Quentin,Dewilde, Anny,Aubry, Jean-Marie,Nardello-Rataj, Véronique

, p. 336 - 345 (2012)

Candidiasis infections are growing problem worldwide especially for the immunocompromised individuals. Di-n-decyldimethylammonium chloride is one of the most common antifungal agents used to clean medical devices. The current study examines the antifungal mechanism of di-n-decyldimethylammonium cation and its cyclodextrin inclusion complexes. Depending on the type of cyclodextrin (α-, β- or γ-CD), inclusion complexes can be as active as ammonium alone in terms of microorganism death (fungicidal activity). Moreover, with β-CD inclusion complexes, synergism is observed against fungus growth (fungistatic activity). Based on molecular dynamics, we propose a mechanism supported by cell number, selective electrode and ζ-potential measurements as a function of time. The mechanism involves four steps: (i) the positively-charged complex diffuses through the solution, (ii) it adsorbs onto the fungus membrane surface by electrostatic interaction, (iii) then it dissociates and the ammonium inserts in the microorganism membrane, and (iv) the change of the cell surface charge induces cell lysis.

Synthesis process of dialkyl dimethyl ammonium chloride

-

Paragraph 0022, (2021/03/11)

The invention discloses a synthesis process of dialkyl dimethyl ammonium halide, which comprises the following steps: mixing primary alkyl halide R1X and long-chain alkyl dimethylamine R2(CH3)2N, heating to 130-150 DEG C in a closed container, keeping the temperature to react for 4-6 hours, cooling, and diluting with an ethanol water solution to obtain dialkyl dimethyl ammonium halide, wherein thereaction temperature is determined by the number of carbon atoms of R1 and R2, and the formula is 130 DEG C+2.5(CR1+CR216)DEG C. Primary alkyl halide and long-chain alkyl dimethylamine directly reactto generate dialkyl dimethyl ammonium halide, so that the use of flammable and combustible gaseous raw materials is avoided, and the production safety is improved, the production process flow and equipment are simple, the production cost is low, industrial popularization is facilitated, no acid or salt byproduct is generated, and the product is high in purity, free of three wastes and environmentally friendly.

Supramolecular assistance between cyclodextrins and didecyldimethylammonium chloride against enveloped viruses: Toward eco-biocidal formulations

Leclercq, Lo?c,Dewilde, Anny,Aubry, Jean-Marie,Nardello-Rataj, Véronique

, p. 273 - 281 (2016/09/07)

Nosocomial infections have emerged as important causes of morbidity and mortality in immunocompromised individuals. In this respect, biocides are widely used in hospitals leading to resistant microorganisms. We show here that cyclodextrins can remarkably boost the virucidal activity of di-n-decyldimethylammonium chloride. These oligosaccharides synergistically work with the biocide affording a noticeable reduction of the active virucide concentration between 40 and 85%. Partial replacement of a significant amount of the biocide by eco- and bio-compatible cyclodextrins whilst maintaining the same activity is of great interest as it allows the reduction of the toxicological drawbacks of classical biocide mixtures.

STABLE COMPOSITIONS OF THIABENDAZOLE AND IODINE-CONTAINING FUNGICIDES

-

, (2015/02/25)

The present invention relates to stable compositions for the fungicidal equipment of thermoplastic polymers, in particular PVC, comprising thiabendazole, at least one iodine-containing fungicide and at least one epoxide and optionally further fungicidally active compounds, and also to methods for preparing these formulations and to uses thereof for the protection of thermoplastic polymers against attack and destruction by microorganisms. Moreover, the invention relates to mold-resistant PVC materials equipped with the compositions according to the invention.

Modeling of multiple equilibria in the self-aggregation of di- n -decyldimethylammonium chloride/octaethylene glycol monododecyl ether/cyclodextrin ternary systems

Leclercq, Loic,Lubart, Quentin,Aubry, Jean-Marie,Nardello-Rataj, Veronique

, p. 6242 - 6252 (2013/07/27)

The surface tension equations of binary surfactant mixtures (di-n-decyldimethylammonium chloride and octaethylene glycol monododecyl ether) are established by combining the Szyszkowski equation of surfactant solutions, the ideal or nonideal mixing theory, and the phase separation model. For surfactant mixtures, the surface tension at the air-water interface is calculated using nonideal theory due to synergism between the two adsorbed surfactant types. The incorporation of cyclodextrin complexation model to the surface tension equations gives a robust model for the description of the surface tension isotherms of binary, ternary, and more complex systems involving numerous inclusion complexes. The surface tension data obtained experimentally shows excellent agreement with the theoretical model below and above the formation of micelles. The strong synergistic effect observed between the two surfactants is disrupted by the presence of CDs, leading to ideal behavior of ternary systems. Indeed, depending on the nature of the cyclodextrin (i.e., α, β, or γ), which allows a tuning of the cavity size, the binding constants with the surfactants are modified as well as the surface properties due to strong modification of equilibria involved in the ternary mixture.

METHOD FOR THE SYNTHESIS OF QUATERNARY AMMONIUM COMPOUNDS AND COMPOSITIONS THEREOF

-

Page/Page column 49-50; 58-59, (2008/06/13)

A novel manufacturing process is described for producing quaternary ammonium compounds having a selected anion, which may be useful in wood preservative formulations. The process involves reacting a trialkylamine with an alkyl bromide to form a quaternary tetraalkylammonium bromide salt, converting the quaternary tetraalkylammonium bromide salt to a quaternary tetraalkylammonium hydroxide salt by using an ion exchange resin, and converting the quaternary tetraalkylammonium hydroxide salt to the quaternary tetraalkylammonium salt of the selected anion.

Synergetic biocidal composition comprising 2-methylisothiazoline-3-on

-

, (2008/06/13)

The invention relates to a biocidal composition which can be added to materials which can be attacked by harmful micro-organisms. The composition comprises 2-methylisothiazoline-3-on as biocidal active ingredient and at least one other biocidal active ingredient. The biocidal composition is characterised in that the composition contains formaldehyde or a formaldehyde-depot material, 2-brom-2-nitro-1,3 propandiol, polyhexamethylene biguanide, o-phenylphenol, pyrithione, n-butyl-1,2-benzisothiazoline-3-on, n-hydroxymenthyl-1,2-benzisothiazoline-3-on or benzalkonium chloride as said other biocidal active ingredient.

3-NITROISOXAZOLES AND THEIR USE IN THE PROTECTION OF MATERIALS

-

, (2012/09/11)

The 3-nitroisoxazoles of the formula (I) in which R1 and R2 are each as defined in the description, some of which are known, are highly suitable for use as biocides for protecting industrial materials.

O-aryl dithiazole dioxides

-

, (2012/09/11)

The invention relates to new O-aryldithiazole dioxides, to two processes for their preparation, and to their use as pesticides in crop protection and in the protection of materials.

Synergistic biocide composition

-

, (2008/06/13)

A biocide composition is provided as an addition to substances that can be infected by harmful microorganisms, in which the biocide composition has at least two active biocidal substances, one of which is 2-methylisothiazolin-3-one. The composition is characterized in that it contains 1,2-benzisothiazolin-3-one, compositions containing 5-chloro-2-methylisothiazolin-3-one being excluded. In comparison with its individual components, the composition of the invention has a synergistic biocidal activity.

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