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
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.
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.
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 |
