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Merck
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74989

Supelco

Octylamine

analytical standard

Sinónimos:

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Fórmula lineal:
CH3(CH2)7NH2
Número de CAS:
111-86-4
Peso molecular:
129.24
Beilstein:
1679227
Número CE:
203-916-0
Número MDL:
MFCD00008247
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329766025

grado

analytical standard

Nivel de calidad

100

presión de vapor

1 mmHg ( 20 °C)

Análisis

≥99.5% (GC)

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

impurezas

≤0.2% water

índice de refracción

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

bp

175-177 °C (lit.)

mp

−5-−1 °C (lit.)

densidad

0.782 g/mL at 25 °C (lit.)

aplicaciones

environmental

formato

neat

cadena SMILES

CCCCCCCCN

InChI

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

Clave InChI

IOQPZZOEVPZRBK-UHFFFAOYSA-N

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Aplicación

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.

Palabra de señalización

Danger

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

140.0 °F - closed cup

Punto de inflamabilidad (°C)

60 °C - closed cup

Equipo de protección personal

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

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Certificados de análisis (COA)

Lot/Batch Number
BCBQ9628V
BCBL7655V
BCBC9202V
BCBC9202
BCBB4488

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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)
Rosario Zamora et al.
Journal of agricultural and food chemistry, 54(6), 2398-2404 (2006-03-16)
The reactions of 4,5-epoxy-2-decenal with octylamine, benzylamine, and 2-phenylglycine methyl ester were studied to investigate if amines may suffer a Strecker type degradation by epoxyalkenals analogously to amino acids. In addition to other reactions, the studied amines were converted into
Hong Zheng et al.
Journal of biomedical nanotechnology, 7(5), 648-658 (2011-12-27)
Quantum dots (QDs) have emerged as alternative or complementary tools to organic fluorescent dyes currently used in bioimaging. QDs hold several advantages over conventional fluorescent dyes including greater photostability and a wider range of excitation/emission wavelengths. However, recent work suggests
Shibin He et al.
Biomaterials, 32(23), 5471-5477 (2011-05-07)
Quantum dots (QDs) have been received most attention due to their unique properties. Constructing QDs conjugated with certain number of biomolecules is considered as one of the most important research goals in nanobiotechnology. In this study, we report polymerase chain
Brad A Kairdolf et al.
Analytical chemistry, 80(8), 3029-3034 (2008-03-08)
Quantum-dot (QD) nanocrystals are promising fluorescent probes for multiplexed staining assays in biological applications. However, nonspecific QD binding to cellular membranes and proteins remains a limiting factor in detection sensitivity and specificity. Here we report a new class of hydroxyl
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