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Merck

52365

Sigma-Aldrich

Bromuro de hexadeciltrimetilamonio

BioUltra, for molecular biology, ≥99.0% (AT)

Sinónimos:

Bromuro de cetiltrimetilamonio, Bromuro de cetrimonio, Bromuro de palmitiltrimetilamonio, CTAB

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About This Item

Fórmula lineal:
CH3(CH2)15N(Br)(CH3)3
Número de CAS:
Peso molecular:
364.45
Beilstein/REAXYS Number:
3598189
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25

grade

for molecular biology

Quality Level

description

cationic

product line

BioUltra

assay

≥99.0% (AT)

form

powder or crystals

mol wt

micellar avg mol wt 62,000

aggregation number

170

impurities

DNases, none detected
RNases, none detected
insoluble matter, passes filter test
phosphatases, none detected
proteases, none detected

ign. residue

≤0.2%

loss

≤0.5% loss on drying

pH

5.0-7.0 (25 °C, 0.1 M in H2O)

CMC

0.92
1 mM (20-25°C)

mp

248-251 °C (lit.)

solubility

H2O: 0.1 M at 40 °C, clear, colorless

anion traces

sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤5 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

[Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C

λ

0.1 M in H2O

UV absorption

λ: 260 nm Amax: 0.06
λ: 280 nm Amax: 0.05

HLB

10

InChI

1S/C19H42N.BrH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2,3)4;/h5-19H2,1-4H3;1H/q+1;/p-1

InChI key

LZZYPRNAOMGNLH-UHFFFAOYSA-M

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Application

Hexadecyltrimethylammonium bromide has been used for the isolation of plant high molecular weight DNA as well as plant DNA for use in PCR analysis. It has also been used to preciptate nucleic acids.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2 Oral - STOT SE 3

target_organs

Gastrointestinal tract, Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

471.2 °F - closed cup

flash_point_c

244 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificados de análisis (COA)

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Lourdes Pérez et al.
European journal of medicinal chemistry, 44(5), 1884-1892 (2008-12-17)
Biocompatible cationic surfactants from the amino acid lysine (hydrochloride salts of N(epsilon)-lauroyl lysine methyl ester, N(epsilon)-myristoyl lysine methyl ester and N(epsilon)-palmitoyl lysine methyl ester) have been prepared in high yields by lysine acylation in epsilon position with three natural saturated
A T Nasr et al.
Physics in medicine and biology, 60(12), 4685-4704 (2015-05-29)
In this study, recipe optimization of Leuco Crystal Violet (LCV) micelle gels made with the surfactant Cetyl Trimethyl Ammonium Bromide (CTAB) and the chemical sensitizer 2,2,2-trichloroethanol (TCE) was aided by a two-level three-factor designed experiment. The optimized recipe contains 0.75
Sebastien Fraud et al.
Antimicrobial agents and chemotherapy, 52(12), 4478-4482 (2008-10-08)
The biocide chlorhexidine (CHX) as well as additional membrane-active agents were shown to induce expression of the mexCD-oprJ multidrug efflux operon, dependent upon the AlgU stress response sigma factor. Hyperexpression of this efflux system in nfxB mutants was also substantially
Fay-Wei Li et al.
Nature communications, 6, 7852-7852 (2015-07-29)
Phytochromes are red/far-red photoreceptors that play essential roles in diverse plant morphogenetic and physiological responses to light. Despite their functional significance, phytochrome diversity and evolution across photosynthetic eukaryotes remain poorly understood. Using newly available transcriptomic and genomic data we show
Armando Maestro et al.
Langmuir : the ACS journal of surfaces and colloids, 31(23), 6289-6297 (2015-05-15)
We address the rheology of assemblies of surfactant-decorated silica nanoparticles irreversibly adsorbed at the gas/liquid interface. Positively charged surfactant molecules (such as CTAB) bind to silica nanoparticle surfaces, and the resulting particle-surfactant complexes adsorb at gas/liquid interfaces. The surfactant molecules

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