Product Name

  • Name

    Dodecyltrimethylammonium chloride

  • EINECS 203-927-0
  • CAS No. 112-00-5
  • Article Data7
  • CAS DataBase
  • Density 0.9265 (rough estimate)
  • Solubility soluble in water
  • Melting Point 237 ºC
  • Formula C15H34N.Cl
  • Boiling Point 412.12°C (rough estimate)
  • Molecular Weight 263.895
  • Flash Point 19°C
  • Transport Information UN 3077 9/PG 3
  • Appearance Light yellow liquid
  • Safety 26-61-60-37/39-36
  • Risk Codes 36/37/38-50-50/53-22-67-11
  • Molecular Structure Molecular Structure of 112-00-5 (Dodecyltrimethylammonium chloride)
  • Hazard Symbols HarmfulXn,DangerousN
  • Synonyms 1-Dodecanaminium,N,N,N-trimethyl-, chloride (9CI);Ammonium, dodecyltrimethyl-, chloride (8CI);Dodecyltrimethylammonium chloride (6CI);Adogen 412;Aliquat 4;CA 2150;Catinal LTC 35A;Catiogen L;Catiogen TML;Cation BB;Cation FB;DTAC;Dehyquart LT;I 0453;Laurtrimonium chloride;Lauryltrimethylammonium chloride;Lauryltrimonium chloride;Monolauryltrimethylammonium chloride;N,N,N-Trimethyl-1-dodecanaminiumchloride;N-Dodecyl-N,N,N-trimethylammonium chloride;Nissan Cation BB;NissanCation BB 300;Nissan Cation FB;Pionin B 111;Quartamin 24;Trimethyldodecylammonium chloride;Trimethyllaurylammoniumchloride;
  • PSA 0.00000
  • LogP 1.61750

Synthetic route

1-chlorododecane
112-52-7

1-chlorododecane

trimethylamine
75-50-3

trimethylamine

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Conditions
ConditionsYield
In methanol; ethanol for 24h; Heating;49%
With ethanol at 80 - 90℃;
With water at 80℃;
methylene chloride
74-87-3

methylene chloride

N,N-dimethylaminododecane
112-18-5

N,N-dimethylaminododecane

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Conditions
ConditionsYield
With pentane at 60℃;
ethanol
64-17-5

ethanol

1-chlorododecane
112-52-7

1-chlorododecane

trimethylamine
75-50-3

trimethylamine

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Conditions
ConditionsYield
analoge Reaktionen mit hoeheren Alkylhalogeniden;
C29H38N6O4*C15H34N(1+)*Cl(1-)

C29H38N6O4*C15H34N(1+)*Cl(1-)

A

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

B

Trp-Aib-Gly-Leu-NHPh
232279-44-6

Trp-Aib-Gly-Leu-NHPh

Conditions
ConditionsYield
In chloroform-d1 at 24.84℃; Equilibrium constant; complex formation;
C31H42N6O4*C15H34N(1+)*Cl(1-)

C31H42N6O4*C15H34N(1+)*Cl(1-)

A

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

B

Trp-Aib-Gly-Leu-NH-C6H3(3,5-Me2)
271770-12-8

Trp-Aib-Gly-Leu-NH-C6H3(3,5-Me2)

Conditions
ConditionsYield
In chloroform-d1 at 24.84℃; Equilibrium constant; complex formation;
dodecylammonium chloride
929-73-7

dodecylammonium chloride

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Conditions
ConditionsYield
With 1-ethyl-3-methylimidazolium bromide at 169.84℃; for 8h;
n-Dodecylamine
124-22-1

n-Dodecylamine

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: aqueous ethanol / 60 - 80 °C
2: skellysolve-A / 60 °C
View Scheme
α,α-dichloro-m-xylene
2719-42-8

α,α-dichloro-m-xylene

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

3-Methylbenzotrichloride
3335-34-0

3-Methylbenzotrichloride

Conditions
ConditionsYield
With sodium hydroxide In tetrachloromethane; water93.4%
sodium tetraphenyl borate
143-66-8

sodium tetraphenyl borate

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

dodecyltrimethylammonium tetraphenylborate

dodecyltrimethylammonium tetraphenylborate

Conditions
ConditionsYield
In water at 85℃; for 1.16667h;92%
potassium tetrachloroaurate(III) dihydrate

potassium tetrachloroaurate(III) dihydrate

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

1-dodecylthiol
112-55-0

1-dodecylthiol

[lauryltrimethylammonium][Au(dodecanethiolate)2]
349490-82-0

[lauryltrimethylammonium][Au(dodecanethiolate)2]

Conditions
ConditionsYield
With sodium methylate In methanol ammonium halide mixed with Au compd. (1:1), suspn. of ammonium chloroaurate treated with thiol (4 equiv.) and NaOMe (4 equiv.); pptd., filtered off, washed (water, MeOH), dried (vac.), elem. anal.;91%
chloroamine-T
127-65-1

chloroamine-T

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

C15H34N(1+)*C7H7ClNO2S(1-)

C15H34N(1+)*C7H7ClNO2S(1-)

Conditions
ConditionsYield
In water at 5℃; for 5h;86%
hexachloroethane
67-72-1

hexachloroethane

3-Methylbenzotrichloride
3335-34-0

3-Methylbenzotrichloride

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

α,α,α,α'-tetrachloro-m-xylene

α,α,α,α'-tetrachloro-m-xylene

Conditions
ConditionsYield
With potassium hydroxide In 1,1,2,2-tetrachloroethylene; water85.2%
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

epichlorohydrin
106-89-8

epichlorohydrin

(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol
100-79-8

(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol

2,2-dimethyl-4-(2',3'-epoxy) propoxymethyl-1,3-dioxolane

2,2-dimethyl-4-(2',3'-epoxy) propoxymethyl-1,3-dioxolane

Conditions
ConditionsYield
With potassium hydroxide In hexane78%
acetone glycerol ketal

acetone glycerol ketal

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

epichlorohydrin
106-89-8

epichlorohydrin

2,2-dimethyl-4-(2',3'-epoxy) propoxymethyl-1,3-dioxolane

2,2-dimethyl-4-(2',3'-epoxy) propoxymethyl-1,3-dioxolane

Conditions
ConditionsYield
With sodium hydroxide In hexane78%
copper (11) chloride dihydrate

copper (11) chloride dihydrate

tris (triphenylphosphine) ruthenium (11) chloride

tris (triphenylphosphine) ruthenium (11) chloride

1-Decene
872-05-9

1-Decene

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Decan-2-one
693-54-9

Decan-2-one

Conditions
ConditionsYield
In water; ethyl acetate; benzene64%
CH(COC4H3NC6H2(O(CH2)15CH3)3)2BF2

CH(COC4H3NC6H2(O(CH2)15CH3)3)2BF2

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

C15H34N(1+)*C119H209BClF2N2O8(1-)

C15H34N(1+)*C119H209BClF2N2O8(1-)

Conditions
ConditionsYield
In 1,4-dioxane Heating;63%
pentacyanocyclopentadienyl anion sodium salt

pentacyanocyclopentadienyl anion sodium salt

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

C10N5(1-)*C15H34N(1+)

C10N5(1-)*C15H34N(1+)

Conditions
ConditionsYield
In water for 0.166667h;39%
copper(II) chloride dihydrate

copper(II) chloride dihydrate

1-Decene
872-05-9

1-Decene

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

palladium dichloride

palladium dichloride

Decan-2-one
693-54-9

Decan-2-one

Conditions
ConditionsYield
In water; ethyl acetate; benzene2%
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Trp-Aib-Gly-Leu-NHPh
232279-44-6

Trp-Aib-Gly-Leu-NHPh

C29H38N6O4*C15H34N(1+)*Cl(1-)

C29H38N6O4*C15H34N(1+)*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 24.84℃; Equilibrium constant; complex formation;
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

Trp-Aib-Gly-Leu-NH-C6H3(3,5-Me2)
271770-12-8

Trp-Aib-Gly-Leu-NH-C6H3(3,5-Me2)

C31H42N6O4*C15H34N(1+)*Cl(1-)

C31H42N6O4*C15H34N(1+)*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 24.84℃; Equilibrium constant; complex formation;
C18H12N2O5S
953077-73-1

C18H12N2O5S

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

C15H34N(1+)*C18H11N2O5S(1-)

C15H34N(1+)*C18H11N2O5S(1-)

Conditions
ConditionsYield
In water; isopropyl alcohol at 80℃; for 2h;
C42H82O17

C42H82O17

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

C15H34N(1+)*C42H81O17(1-)

C15H34N(1+)*C42H81O17(1-)

Conditions
ConditionsYield
With potassium hydroxide In water pH=7;
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

3-Methyl-2-nitrobenzal chloride
99318-68-0

3-Methyl-2-nitrobenzal chloride

2-nitro-3-methyl benzyl chloride
70018-11-0

2-nitro-3-methyl benzyl chloride

3-Methyl-2-nitrobenzotrichloride
99318-66-8

3-Methyl-2-nitrobenzotrichloride

Conditions
ConditionsYield
With sodium hydroxide In tetrachloromethane; dichloromethane; tert-butyl alcohol
3-bromomethylthiophene-2-sulfonamide
111283-83-1

3-bromomethylthiophene-2-sulfonamide

2,2,2-trifluoroethanol
75-89-8

2,2,2-trifluoroethanol

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

3-(2,2,2-trifluoroethoxymethyl)-2-thiophenesulfonamide

3-(2,2,2-trifluoroethoxymethyl)-2-thiophenesulfonamide

Conditions
ConditionsYield
With sodium hydroxide In water
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

dodecyltrimethylammonium tetracarbonylcobaltate

dodecyltrimethylammonium tetracarbonylcobaltate

Conditions
ConditionsYield
In sodium hydroxide; toluene the Co-compd. and the chloride are dissolved in a degassed mixt. of 5 MNaOH and toluene under CO, stirring of the soln. for 40 min; removal of the org. phase (syringe) and drying (MgSO4) under CO;
lithium cobalt(III) oxide

lithium cobalt(III) oxide

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

[C12H25N(CH3)3]0.4Li0.4CoO2

[C12H25N(CH3)3]0.4Li0.4CoO2

[(DPPE)((C6H5)2P(CH2)2P(C6H5)(C6H4))Ru](PF6)
199533-73-8

[(DPPE)((C6H5)2P(CH2)2P(C6H5)(C6H4))Ru](PF6)

trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

(DPPE)((C6H5)2PCH2CH2P(C6H5)(C6H4))RuCl

(DPPE)((C6H5)2PCH2CH2P(C6H5)(C6H4))RuCl

Conditions
ConditionsYield
In dichloromethane-d2 room temp.;
trimethyldodecylammonium chloride
112-00-5

trimethyldodecylammonium chloride

dermatan sulfate

dermatan sulfate

dermatan sulfate dodecyltrimethylammonium salt

dermatan sulfate dodecyltrimethylammonium salt

Conditions
ConditionsYield
In water

Dodecyl trimethyl ammonium chloride Specification

The IUPAC name of Lauryltrimethylammonium chloride is dodecyl(trimethyl)azanium chloride. With the CAS registry number 112-00-5, it is also named as N,N,N-Trimethyl-1-dodecanaminium chloride. The product's categories are Alkylamine Salts & Quarternary Ammonium Salts (Surfactants); Ammonium Chlorides (Quaternary); Cationic Surfactants; Functional Materials; Quaternary Ammonium Compounds; Surfactants; Analytical Chemistry; HPLC Ion-Pair Reagents for Acidic Samples; Ion-Pair Reagents for HPLC; Water Ttreatment Chemicals; Ammonium Salts; Phase Transfer Catalysts. It is light yellow liquid which is hygroscopic and resistant to heat, light, strong acid and alkali. Additionally, this chemical should be sealed in the container and stored in the cool and dry place.

The other characteristics of this product can be summarized as: (1)ACD/LogP: 0.67; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.67; (4)ACD/LogD (pH 7.4): 0.67; (5)ACD/BCF (pH 5.5): 1.91; (6)ACD/BCF (pH 7.4): 1.91; (7)ACD/KOC (pH 5.5): 55.39; (8)ACD/KOC (pH 7.4): 55.39; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 11; (12)Rotatable Bond Count: 11; (13)Exact Mass: 263.237978; (14)MonoIsotopic Mass: 263.237978; (15)Heavy Atom Count: 17; (16)Complexity: 135.

Preparation of Lauryltrimethylammonium chloride: Adding 430kg N,N-dimethyldodecylamine into the reactor, and then adding a certain amount of isopropyl alcohol and water into the reactor. Using alkali as catalyst. After the replacement of the air of pressure vessel, it gradually warming and leading to 111kg monochlorosilane at 0.2 ~ 0.3MPa to react 4h. After cooling to atmospheric pressure, we can get the products.

Uses of Lauryltrimethylammonium chloride: It can be used as catalysts, emulsifiers, fungicides, disinfectants, antistatic agents, cationicsurfactant and so on. And it can react with N-chloro-toluene-4-sulfonamide; sodium salt to get C15H34N1+*C7H7ClNO2S1-. This reaction needs solvent water at temperature of 5 °C. The reaction time is 5 hours. The yield is 86%.

When you are using this chemical, please be cautious about it as the following:
It is highly flammable, harmful if swallowed and irritating to eyes, respiratory system and skin. Moreover, this chemical is very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. This material and its container must be disposed of as hazardous waste. 

People can use the following data to convert to the molecule structure.
1. SMILES:[Cl-].C(CCCC[N+](C)(C)C)CCCCCCC
2. InChI:InChI=1/C15H34N.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16(2,3)4;/h5-15H2,1-4H3;1H/q+1;/p-1

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LDLo oral 300mg/kg (300mg/kg)   National Technical Information Service. Vol. OTS0543823,

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