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74989

Supelco

Octylamine

analytical standard

Synonym(s):

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Linear Formula:
CH3(CH2)7NH2
CAS Number:
Molecular Weight:
129.24
Beilstein:
1679227
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

Quality Level

vapor pressure

1 mmHg ( 20 °C)

Assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.2% water

refractive index

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

bp

175-177 °C (lit.)

mp

−5-−1 °C (lit.)

density

0.782 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

CCCCCCCCN

InChI

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

InChI key

IOQPZZOEVPZRBK-UHFFFAOYSA-N

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Application

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.

Signal Word

Danger

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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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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