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Merck
CN

74990

Octylamine

puriss., ≥99.0% (GC)

Synonym(s):

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Linear Formula:
CH3(CH2)7NH2
CAS Number:
111-86-4
Molecular Weight:
129.24
EC Number:
203-916-0
UNSPSC Code:
12352100
PubChem Substance ID:
329766027
Beilstein/REAXYS Number:
1679227
MDL number:
MFCD00008247

Key Documents

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vapor pressure

1 mmHg ( 20 °C)

grade

puriss.

assay

≥99.0% (GC)

refractive index

n20/D 1.429 (lit.), n20/D 1.430

bp

175-177 °C (lit.)

mp

−5-−1 °C (lit.)

density

0.782 g/mL at 25 °C (lit.)

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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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

3 - Flammable liquids

wgk

WGK 3

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

ppe

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

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Anna-Karin Hellström et al.
Journal of colloid and interface science, 511, 84-91 (2017-10-11)
Carbon dioxide is commonly used as pH regulator in switchable surfactant systems and in the formation of alkyl ammonium-alkyl carbamate ion-pair. Its use to form a meta-stable anionic surfactant has been less explored and can impart a cleavable character to
Takanari Togashi et al.
Dalton transactions (Cambridge, England : 2003), 46(37), 12487-12493 (2017-09-13)
Metal oxalates (C
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
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
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
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