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Key Documents

74989

Supelco

Octylamine

analytical standard

Sinônimo(s):

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Fórmula linear:
CH3(CH2)7NH2
Número CAS:
Peso molecular:
129.24
Beilstein:
1679227
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:

grau

analytical standard

Nível de qualidade

pressão de vapor

1 mmHg ( 20 °C)

Ensaio

≥99.5% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

Impurezas

≤0.2% water

índice de refração

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

pb

175-177 °C (lit.)

pf

−5-−1 °C (lit.)

densidade

0.782 g/mL at 25 °C (lit.)

aplicação(ões)

environmental

formato

neat

cadeia de caracteres SMILES

CCCCCCCCN

InChI

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

chave InChI

IOQPZZOEVPZRBK-UHFFFAOYSA-N

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Aplicação

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.

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

140.0 °F - closed cup

Ponto de fulgor (°C)

60 °C - closed cup

Equipamento de proteção individual

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


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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

Protocolos

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

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