Merck
CN

52365

Sigma-Aldrich

溴化十六烷基三甲铵

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

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别名:
CTAB, 溴化十六烷基三甲铵, 溴棕三甲铵, 鲸蜡烷三甲基溴化铵
线性分子式:
CH3(CH2)15N(Br)(CH3)3
CAS号:
分子量:
364.45
Beilstein:
3598189
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.25

等级

for molecular biology

质量水平

描述

cationic

产品线

BioUltra

检测方案

≥99.0% (AT)

形式

powder or crystals

分子量

micellar avg mol wt 62,000

聚集数

170

杂质

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

灼烧残渣

≤0.2%

缺失

≤0.5% loss on drying

pH值(酸碱度)

5.0-7.0 (25 °C, 0.1 M in H2O)

CMC

0.92
1 mM (20-25°C)

mp

248-251 °C (lit.)

溶解性

H2O: 0.1 M at 40 °C, clear, colorless

痕量阴离子

sulfate (SO42-): ≤50 mg/kg

痕量阳离子

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

紫外吸收

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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应用

十六烷基三甲基溴化铵已被用于分离植物高分子量 DNA 以及用于 PCR 分析的植物 DNA。也用于沉淀核酸。

警示用语:

Danger

危险分类

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

靶器官

Gastrointestinal tract, Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

471.2 °F - closed cup

闪点(°C)

244 °C - closed cup

个人防护装备

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


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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
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
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
A T Nasr et al.
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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

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