n-Dodecylamine hydrochloride

Product Information

Molecular Formula:
C12H28ClN
Molecular Weight:
221.81
Description
n-Dodecylamine hydrochloride is a pharmaceutical-grade compound widely used in the biomedical industry. It exhibits potent antimicrobial properties, making it essential in the development of drugs targeting bacterial infections. Additionally, this hydrochloride is employed in the drug development of skin disorders, respiratory diseases, and urinary tract infections.
Synonyms
1-Dodecanamine,hydrochloride; dodecanaminehydrochloride; dodecylammoniumchloride; laurylammoniumhydrochloride; n-dodecylammoniumchloride; N-DODECYLAMINE HCL; N-DODECYLAMINE HYDROCHLORIDE; TIMTEC-BB SBB003344
IUPAC Name
dodecan-1-aminehydrochloride
Canonical SMILES
CCCCCCCCCCCCN.Cl
InChI
InChI=1S/C12H27N.ClH/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-13H2,1H31H
InChI Key
TWFQJFPTTMIETC-UHFFFAOYSA-N
Boiling Point
258.6°C at 760mmHg
Melting Point
186-188°C
Purity
95%
Appearance
white powder
Vapor Pressure
0.00000008 [mmHg]

Safety Information

Hazards
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P270:
Do not eat, drink or smoke when using this product.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312+P330:
IF SWALLOWED:
Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
10
Exact Mass
221.1910276 g/mol
Monoisotopic Mass
221.1910276 g/mol
Topological Polar Surface Area
26Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
81.2
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
US-2003235916-A1 Novel methods for the delivery of polynucleotides to cells 2002-06-14
US-5376686-A Biguanide derivatives, manufacturing method thereof, and disinfectants containing the derivatives 1991-04-05
US-4530714-A N-aliphatic and N,N-aliphatic phosphoric triamide urease inhibitors and urease inhibited urea based fertilizer compositions 1983-03-16

Literatures

PMID Publication Date Title Journal
22983592 2012-10-12 Targeting etoposide to acute myelogenous leukaemia cells using nanostructured lipid carriers coated with transferrin Nanotechnology
22776375 2012-10-01 Effects of wet heat treatment on the germination of individual spores of Clostridium perfringens Journal of applied microbiology
22840533 2012-10-01 Effective collection of hydrophobic organic pollutants in water with aluminum hydroxide and hydrophobically modified polyacrylic acid Chemosphere
22683185 2012-07-20 Highly stable high performance liquid chromatography stationary phase based on direct chemical modification of organic bridges in hybrid silica Journal of chromatography. A
22440729 2012-06-01 Close-packed monolayers of charged Janus-type nanoparticles at the air-water interface Journal of colloid and interface science
22023906 2011-12-30 Recovery of synthetic dye from simulated wastewater using emulsion liquid membrane process containing tri-dodecyl amine as a mobile carrier Journal of hazardous materials
22098933 2011-12-30 Phase transfer membrane supported liquid-liquid-liquid microextraction combined with large volume sample injection capillary electrophoresis-ultraviolet detection for the speciation of inorganic and organic mercury Journal of chromatography. A
21982993 2011-11-11 Preparative separation of 1,3,6-pyrenetrisulfonic acid trisodium salt from the color additive D&C Green No. 8 (pyranine) by pH-zone-refining counter-current chromatography Journal of chromatography. A
21384897 2011-03-30 Electron transfer between colloidal ZnO nanocrystals Journal of the American Chemical Society
21324466 2011-03-25 Selective extraction of emerging contaminants from water samples by dispersive liquid-liquid microextraction using functionalized ionic liquids Journal of chromatography. A
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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