Dodecyl trimethyl ammonium chloride

Product Information

Molecular Formula
C15H34N?Cl
Molecular Weight
263.89
Description
Dodecyl trimethyl ammonium chloride is an extensively utilized biomedical product that showcases notable attributes as an antimicrobial agent. Its remarkable bactericidal and fungicidal capabilities confer efficacy against a myriad of drug-resistant pathogens, thereby rendering it a formidable tool for combatting infections instigated by both bacteria and fungi.
Synonyms
LTAC; LAURYLTRIMETHYLAMMONIUM CHLORIDE; IPC-DTMA-CL; DODECYLTRIMETHYLAMMONIUM CHLORIDE; DTAC; N-DODECYLTRIMETHYLAMMONIUM CHLORIDE
IUPAC Name
dodecyl(trimethyl)azaniumchloride
Canonical SMILES
CCCCCCCCCCCC[N+](C)(C)C.[Cl-]
InChI
InChI=1S/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
InChI Key
DDXLVDQZPFLQMZ-UHFFFAOYSA-M
Boiling Point
412.12°C
Melting Point
237°C
Flash Point
19 °C
Purity
>98.0%(T)
Solubility
water, 1795 mg/L @ 25 °C (est)
Appearance
white solid
Application
Quaternary ammonium salts useful as paint strippers, foaming stabilizers, and bactericidal lotions.
Storage
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture.
Refractive Index
n20/D 1.426
Stability
Stable. Incompatible with strong oxidizing agents. Protect from moisture.
Vapor Pressure
0.00000001 [mmHg]

Safety Information

Hazards
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H410:
Very toxic to aquatic life with long-lasting effects.
Precautionary Statement
P264:
Wash thoroughly after handling.
P273:
Avoid release to the environment.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P391:
Collect spillage.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
11
Exact Mass
263.2379778 g/mol
Monoisotopic Mass
263.2379778 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
135
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114058360-A Multifunctional suspension concentrated fracturing fluid and preparation method thereof 2022-01-17
CN-114149865-A Method for extracting peony essential oil from surfactant aqueous solution 2022-01-14
CN-114032551-A Preparation method of ternary composite quaternary ammonium salt corrosion inhibitor 2022-01-12
CN-114106233-A Preparation method of novel compression-resistant antibacterial super absorbent resin 2021-12-31
CN-114045107-A Environment-friendly high-solid-content aqueous polyurethane acrylate composite emulsion and preparation method and application thereof 2021-12-30
CN-113980580-A Alkali etching polishing method for monocrystalline silicon wafer 2021-12-24
CN-114106436-A Degradable butyronitrile gloves and preparation method thereof 2021-12-24
CN-114149381-A Preparation method of 2, 3-dihydro-5-methyl-2-oxo-1, 3, 4-oxadiazole-3-acetone 2021-12-22
CN-114105527-A Permeable asphalt and preparation method thereof 2021-12-21
CN-114133576-A Polyphosphate flame retardant containing benzene ring structure and synthesis method thereof 2021-12-17

Literatures

PMID Publication Date Title Journal
22197735 2012-11-01 Salt effect on microscopic structure and stability of colloidal complex obtained from neutral/polyelectrolyte block copolymer and oppositely charged surfactant Colloids and surfaces. B, Biointerfaces
22842797 2012-10-07 Microfluidic sensing devices employing in situ-formed liquid crystal thin film for detection of biochemical interactions Lab on a chip
22877504 2012-09-26 One-pot synthesis of dendritic gold nanostructures in aqueous solutions of quaternary ammonium cationic surfactants: effects of the head group and hydrocarbon chain length ACS applied materials & interfaces
22760506 2012-09-01 Study on the effect of chain-length compatibility of mixed anionic-cationic surfactants on the cloud-point extraction of selected organophosphorus pesticides Analytical and bioanalytical chemistry
22608143 2012-08-01 Spontaneous vesicles, disks, threadlike and spherical micelles found in the solubilization of DMPC liposomes by the detergent DTAC Journal of colloid and interface science
22691921 2012-07-21 Aqueous phase behavior of polyelectrolytes with amphiphilic counterions modulated by cyclodextrin: the role of polyion flexibility Physical chemistry chemical physics : PCCP
22498365 2012-07-01 Electroless deposition of Ni-P-nano-ZrO2 composite coatings in the presence of various types of surfactants Journal of colloid and interface science
22592986 2012-06-30 Analysis of plasma nucleotides in rat by micellar electrokinetic capillary chromatography/electrospray ionization mass spectrometry Rapid communications in mass spectrometry : RCM
22444485 2012-06-15 Solubilization of two organic dyes by cationic ester-containing gemini surfactants Journal of colloid and interface science
22265914 2012-05-30 Nanocomposite formation between alpha-glucosyl stevia and surfactant improves the dissolution profile of poorly water-soluble drug International journal of pharmaceutics
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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