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Fórmula lineal:
CH3(CH2)7N(CH3)2
Número CAS:
Peso molecular:
157.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-939-3
Beilstein/REAXYS Number:
1698081
MDL number:
Assay:
95%
Form:
liquid
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlevapor density
5.4 (vs air)
Quality Level
vapor pressure
0.8 mmHg ( 25 °C)
assay
95%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
195 °C (lit.)
mp
−57 °C (lit.)
density
0.765 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCCCCCCCN(C)C
InChI
1S/C10H23N/c1-4-5-6-7-8-9-10-11(2)3/h4-10H2,1-3H3
InChI key
UQKAOOAFEFCDGT-UHFFFAOYSA-N
Application
N,N-Dimethyloctylamine has been employed:
- as ion-pairing agent in quantitative estimation of thiazinamium methylsulphate in a pharmaceutical preparation by HPLC
- as counterion in mobile phase for separation of tetracycline, tetracycline analogs and their potential impurities by reversed-phase ion-pair chromatography
- as mobile phase in direct resolution and quantitation of (R)- and (S)-disopyramide in human plasma
- in study of chiral separations by complexation with proteins in capillary zone electrophoresis
signalword
Danger
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Skin Sens. 1
Clase de almacenamiento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Journal of Chromatography A, 635, 119-119 (1993)
T T Nikiforov et al.
Analytical biochemistry, 227(1), 201-209 (1995-05-01)
A reliable, simple, and cost-effective method for the immobilization of relatively short (12-30 mer) oligonucleotide probes to 96-well polystyrene plates was required in our laboratory for use in DNA hybridization-based assays. We compared three different approaches to achieve this immobilization.
J Hermansson et al.
Journal of pharmaceutical sciences, 71(2), 222-229 (1982-02-01)
Methods are presented for the separation of tetracycline, tetracycline analogs, and their potential impurities by reversed-phase ion-pair chromatography. The mobile phase consisted of a phosphate buffer with tripropylamine or N,N-dimethyloctylamine as counterions and acetonitrile as the organic modifier. The chromatographic



