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Tetradecyltrimethylammonium bromide

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Tetradecyltrimethylammonium bromide Basic information

Product Name:
Tetradecyltrimethylammonium bromide
Synonyms:
  • alkyl*trimethylammoniumbromide*(c14,5%c16)
  • alkyltrimethylammoniumbromide
  • alkyltrimethylammoniumbromide(c14,5%c16)
  • Tetradecanaminium,N,N,N-trimethyl-,bromide
  • tetradecyltrimethyl-ammoniubromide
  • MYRTRIMONIUM BROMIDE
  • (1-Tetradecyl)trimethylammonium bromide
  • TETRADECYLTRIMETHYLAMMONIUM BROMIDE, FOR IPC
CAS:
1119-97-7
MF:
C17H38N.Br
MW:
336.39
EINECS:
214-291-9
Product Categories:
  • Pharmaceutical raw materials
  • Ammonium Bromides (Quaternary)
  • Quaternary Ammonium Compounds
  • 1119-97-7
Mol File:
1119-97-7.mol
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Tetradecyltrimethylammonium bromide Chemical Properties

Melting point:
245-250 °C(lit.)
Density 
1.1328 (rough estimate)
vapor pressure 
0Pa at 25℃
refractive index 
1.5260 (estimate)
storage temp. 
Store below +30°C.
solubility 
H2O: 10 % (w/v)
form 
Fine Crystalline Powder
color 
White
PH
pH (50g/l, 25℃ : 4.0~6.0
Water Solubility 
20 g/100 mL
Sensitive 
Hygroscopic
λmax
λ: 240 nm Amax: ≤0.08
λ: 250 nm Amax: ≤0.05
λ: 260 nm Amax: ≤0.04
λ: 500 nm Amax: ≤0.02
Merck 
14,6336
BRN 
3633227
Stability:
Stable. Hygroscopic. Incompatible with strong oxidizing agents.
InChIKey
CXRFDZFCGOPDTD-UHFFFAOYSA-M
LogP
2.2 at 20℃
CAS DataBase Reference
1119-97-7(CAS DataBase Reference)
EPA Substance Registry System
Tetradecyl trimethyl ammonium bromide (1119-97-7)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45-27
RIDADR 
UN 3263 8/PG 2
WGK Germany 
3
RTECS 
BS5776000
3
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29239000
Toxicity
LD50 in mice, rats (mg/kg): 12.0, 15.0 i.v. (Issomaa, Bjondahl)

MSDS

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Tetradecyltrimethylammonium bromide Usage And Synthesis

Physical properties

Cetrimide is a white fine powder crystal with a melting point of 245°C to 250°C. A rough estimate of its density is 1.1328. It is soluble in water with a solubility of 20 g/100 mL.

Description

MiTMAB (1119-97-7) is a dynamin I/II inhibitor targeting the dynamin-phospholipid interaction and inhibiting dynamin GTPase activity with a Ki=940nM.1 Rapidly and reversibly inhibits multiple forms of endocytosis with no acute cellular damage1. A useful pharmacological tool for studying dynamin-mediated trafficking events.2 Induces cytokinesis failure and apoptosis in human cancer cells.3 Induces cytoprotective autophagy in human Jurkat T cells.4

Uses

Myristyltrimethylammonium has been used in a study to assess a surfactant-controlled synthetic method to obtain a nanophase of mesoporous ceria-zirconia solid solution containing cationic defects in the crystalline structure.??It has also been used in a study to determine the low molecular weight of organic acids in soils and plants by capillary zone electrophoresis.

Uses

Disinfectant; deodorant; laboratory reagent.

Definition

Myristyltrimethylammonium bro-mide.

General Description

Myristyltrimethylammonium bromide is a cationic/zwitterionic type of surfactant.

Purification Methods

Crystallise the bromide from acetone or a mixture of Me2CO and >5% MeOH or Me2CO/EtOH. Wash it with diethyl ether and dry it in a vacuum oven at 60o. It is a cationic detergent. Its solubility is 1g/5g H2O. [Dearden & Wooley J Phys Chem 91 2404 1987, Shelton et al. J Am Chem Soc 68 754 1946, Beilstein 4 III 419, 4 IV 813.]

References

1) Quan et al. (2007), Myristal trimethyl ammonium bromide and octadecyl trimethyl ammonium bromide are surface-active small molecules dynamin inhibitors that block endocytosis mediated by dynamin I or dynamin II; Mol. Pharmacol., 72 1425 2) Joshi et al. (2011), Development and validation of a stability indicating method for the enantioselective estimation of omeprazole enantiomers in the enteric-coated formulations by high performance liquid chromatography; Mol. Cancer, 104 78 3) De Beco et al. (2009), Endocytosis is required for E-cadherin redistribution at mature adherens junctions; Proc. Natl. Acad. Sci. USA, 106 7010 4) Kim et al. (2016), Inhibition of autophagy enhances dynamin inhibitor-induced apoptosis via promoting Bak activation and mitochondrial damage in human Jurkat T cells; Biochem. Biophys. Res. Commun., 478 1609

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