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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