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Merck

74989

Supelco

Octylamin

analytical standard

Synonym(e):

1-Amino-octan, n-Octylamin, Caprylamin

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About This Item

Lineare Formel:
CH3(CH2)7NH2
CAS-Nummer:
Molekulargewicht:
129.24
Beilstein:
1679227
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:

Qualität

analytical standard

Qualitätsniveau

Dampfdruck

1 mmHg ( 20 °C)

Assay

≥99.5% (GC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Verunreinigungen

≤0.2% water

Brechungsindex

n20/D 1.429 (lit.)
n20/D 1.429

bp

175-177 °C (lit.)

mp (Schmelzpunkt)

−5-−1 °C (lit.)

Dichte

0.782 g/mL at 25 °C (lit.)

Anwendung(en)

environmental

Format

neat

SMILES String

CCCCCCCCN

InChI

1S/C8H19N/c1-2-3-4-5-6-7-8-9/h2-9H2,1H3

InChIKey

IOQPZZOEVPZRBK-UHFFFAOYSA-N

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Anwendung

Octylamine may be used as an ion pairing reagent for the separation and determination of biogenic amines and precursor aminoacids in various food samples using ion-pair high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

140.0 °F - closed cup

Flammpunkt (°C)

60 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

Ion-pair HPLC determination of biogenic amines and precursor aminoacids. Application of a method based on simultaneous use of heptanesulphonate and octylamine to some foods
Arlorio.M, et al.
Chromatographia, 48(11-12), 763-769 (1998)
Vasilios Kimiskidis et al.
Journal of pharmaceutical and biomedical analysis, 43(2), 763-768 (2006-09-09)
An isocratic reversed-phase HPLC-UV procedure for the determination of oxcarbazepine and its main metabolites 10-hydroxy-10,11-dihydrocarbamazepine and 10,11-dihydroxy-trans-10,11-dihydrocarbamazepine in human plasma and cerebrospinal fluid has been developed and validated. After addition of bromazepam as internal standard, the analytes were isolated from
Daniel Barkan et al.
Chemistry & biology, 16(5), 499-509 (2009-05-30)
Mycobacterium tuberculosis infection remains a major global health problem complicated by escalating rates of antibiotic resistance. Despite the established role of mycolic acid cyclopropane modification in pathogenesis, the feasibility of targeting this enzyme family for antibiotic development is unknown. We
Yong-Qin Lv et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 871(1), 1-6 (2008-07-22)
n-Octylamine-modified poly(methacrylate-co-ethylene dimethacrylate) monoliths were prepared for rapid screening, determination and one-step purification of puerarin from Radix puerariae (a crude extract of the root of Pueraria lobata). The modified monolith showed a specific surface area of 17.8 m(2) g(-1), an
Vera Bocharova et al.
Small (Weinheim an der Bergstrasse, Germany), 2(7), 910-916 (2006-12-29)
Spin-coating of isolated positively charged macromolecules onto mica in the presence of octylamine was found to be a simple and general method of stretching and aligning the macromolecular chains. The contour length and molar mass for the stretched macromolecules can

Protokolle

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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