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Merck
CN

30692

Decylamine

≥99.0% (GC)

Synonym(s):

1-Aminodecane, NDA

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About This Item

Linear Formula:
CH3(CH2)9NH2
CAS Number:
2016-57-1
Molecular Weight:
157.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57648462
EC Number:
217-957-7
Beilstein/REAXYS Number:
1735220
MDL number:
MFCD00008149
Assay:
≥99.0% (GC)
Form:
liquid

Key Documents

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InChI key

MHZGKXUYDGKKIU-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCN

assay

≥99.0% (GC)

form

liquid

impurities

≤0.5% water

Quality Level

100

bp

216-218 °C (lit.)

mp

12-14 °C (lit.)

density

0.787 g/mL at 25 °C (lit.)

functional group

amine

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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. It was also used as a coordinating solvent to thermolyse the lead piperidine and lead tetrahydroquinoline dithiocarbamate (DTC) complexes.

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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

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
BCCP3922
BCCP3908
BCCP3180
BCCP0287
BCCN3780

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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)
Aneta D Petelska et al.
Colloids and surfaces. B, Biointerfaces, 82(2), 340-344 (2010-10-05)
Monolayers of phosphatidylcholine, fatty acid and amine and binary mixtures phosphatidylcholine-fatty acid or phosphatidylcholine-amine were investigated at the air/water interface. Phosphatidylcholine (lecithin, PC), stearic acid (SA), palmitic acid (PA), decanoic acid (DA) and decylamine (DE) were used to the experiment.
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
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
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
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