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30692

Sigma-Aldrich

Decylamine

≥99.0% (GC)

Synonym(s):

1-Aminodecane, NDA

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5 ML
$41.00
25 ML
$223.00

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5 ML
$41.00
25 ML
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About This Item

Linear Formula:
CH3(CH2)9NH2
CAS Number:
2016-57-1
Molecular Weight:
157.30
Beilstein/REAXYS Number:
1735220
EC Number:
217-957-7
MDL number:
MFCD00008149
UNSPSC Code:
12352100
PubChem Substance ID:
57648462
NACRES:
NA.22

$41.00

Available to ship onApril 15, 2025Details

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assay

≥99.0% (GC)

form

liquid

impurities

≤0.5% water

refractive index

n20/D 1.436 (lit.)

bp

216-218 °C (lit.)

mp

12-14 °C (lit.)

density

0.787 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCCCCCCN

InChI

1S/C10H23N/c1-2-3-4-5-6-7-8-9-10-11/h2-11H2,1H3

InChI key

MHZGKXUYDGKKIU-UHFFFAOYSA-N

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Application

Decylamine was used in the synthesis of dynole 2-24 series by undergoing reductive amination with 1-(3-(dimethylamino)propyl)-1H-indole-3-carbaldehyde[1]. It was also used as a coordinating solvent to thermolyse the lead piperidine and lead tetrahydroquinoline dithiocarbamate (DTC) complexes[2].

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

192.2 °F - closed cup

flash_point_c

89 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5783
BCCL4674
BCCK6913
BCCH2066
BCCJ7174

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Linda D Nyamen et al.
Dalton transactions (Cambridge, England : 2003), 41(27), 8297-8302 (2012-05-30)
We report the synthesis of lead piperidine and lead tetrahydroquinoline dithiocarbamate (DTC) complexes and their use as single source precursors for the preparation of anisotropic PbS nanoparticles. The complexes were thermolysed in coordinating solvents such hexadecylamime (HDA), tri-n-octylphosphine oxide (TOPO)
Mark J Robertson et al.
Nature protocols, 9(4), 851-870 (2014-03-22)
Dynamin is a large GTPase with roles in membrane fission during clathrin-mediated endocytosis, in actin dynamics and in cytokinesis. Defects in dynamin have been linked to human diseases. The synthesis of a dynamin modulator toolkit comprising two different inhibitor classes
Rebecca A Bader et al.
Biomacromolecules, 12(2), 314-320 (2011-01-12)
Despite improvements relative to unmodified counterparts, poly(ethylene glycol) (PEG) conjugation may not be the ideal solution for improving circulatory stability of current nanoparticle carriers or free drugs. Polysialic acid (PSA), a natural polymer for which the body possesses no receptors
M Tenne et al.
Journal of neurochemistry, 44(5), 1373-1377 (1985-05-01)
Deamination of n-octylamine and n-decylamine has been studied in various tissues using a new bioluminescence technique. Selectivity of n-octylamine and n-decylamine as substrates for monoamine oxidase (MAO) A or B has been determined using both clorgyline and (-)-deprenyl inhibition curves
E R Christensen et al.
Environmental toxicology and chemistry, 20(10), 2361-2369 (2001-10-13)
The joint toxicity of nonylamine and decylamine and of atrazine and decylamine was evaluated in assays with the green alga Selenastrum capricornutum based on an isobologram method. In this method, curves of constant response, isoboles, are plotted versus concentrations of
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