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75091

Sigma-Aldrich

Trimethyloctylammonium bromide

≥98.0% (AT)

Sinónimos:

Octyltrimethylammonium bromide

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About This Item

Fórmula lineal:
CH3(CH2)7N(CH3)3(Br)
Número de CAS:
2083-68-3
Peso molecular:
252.23
Beilstein/REAXYS Number:
3628448
MDL number:
MFCD00051873
UNSPSC Code:
12352116
PubChem Substance ID:
57652549
NACRES:
NA.22

assay

≥98.0% (AT)

form

powder

SMILES string

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

InChI

1S/C11H26N.BrH/c1-5-6-7-8-9-10-11-12(2,3)4;/h5-11H2,1-4H3;1H/q+1;/p-1

InChI key

XCOHAFVJQZPUKF-UHFFFAOYSA-M

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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N B Cech et al.
Analytical chemistry, 73(19), 4632-4639 (2001-10-19)
The effect of uneven fissioning of mass and charge from electrospray droplets on the amount of analyte charged during the electrospray process was explored. A surface selectivity factor (S) was developed to describe the affinity of an analyte for the
[Analysis of supramolecules and noncovalent interactions by mass spectrometry].
D Nohara et al.
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 46(12), 1855-1861 (2001-09-13)
Tonic and phasic block of mammalian sodium currents by charged and neutral n-octyl derivatives.
A A Elliott et al.
Annals of the New York Academy of Sciences, 625, 311-314 (1991-01-01)
Sudhir Husale et al.
Nucleic acids research, 36(5), 1443-1449 (2008-01-22)
The interaction of cationic surfactants with single dsDNA molecules has been studied using force-measuring optical tweezers. For hydrophobic chains of length 12 and greater, pulling experiments show characteristic features (e.g. hysteresis between the pulling and relaxation curves, force-plateau along the
J G Foulks et al.
Canadian journal of physiology and pharmacology, 62(4), 350-355 (1984-04-01)
The local anaesthetic effect of cationic, anionic, and neutral alkyl amphipathic agents was similarly enhanced in an apparently nonspecific way by circumstances which modulate electrostatic interactions (acidity, modification of charged groups at the sarcolemmal surface by group-specific reagents, or changes
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