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74989

Supelco

Octylamine

analytical standard

Sinonimo/i:

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Formula condensata:
CH3(CH2)7NH2
Numero CAS:
111-86-4
Peso molecolare:
129.24
Beilstein:
1679227
Numero CE:
203-916-0
Numero MDL:
MFCD00008247
Codice UNSPSC:
41116107
ID PubChem:
329766025

Grado

analytical standard

Livello qualitativo

100

Tensione di vapore

1 mmHg ( 20 °C)

Saggio

≥99.5% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Impurezze

≤0.2% water

Indice di rifrazione

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

P. ebollizione

175-177 °C (lit.)

Punto di fusione

−5-−1 °C (lit.)

Densità

0.782 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

CCCCCCCCN

InChI

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

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Applicazioni

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.

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

140.0 °F - closed cup

Punto d’infiammabilità (°C)

60 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCBQ9628V

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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
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Protocolli

GC Analysis of Primary Amines on Carbowax® Amine

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

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