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MilliporeSigma

30692

Sigma-Aldrich

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
Beilstein/REAXYS Number:
1735220
EC Number:
217-957-7
MDL number:
MFCD00008149
UNSPSC Code:
12352100
PubChem Substance ID:
57648462
NACRES:
NA.22

Key Documents

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Quality Level

100

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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Show Differences

1 of 4

This Item
D2404D22220882100
Decylamine ≥99.0% (GC)

Sigma-Aldrich

30692

Decylamine

Decylamine 95%

Sigma-Aldrich

D2404

Decylamine

Dodecylamine 98%

Sigma-Aldrich

D222208

Dodecylamine

Propylamine purum, ≥99.0% (GC)

Sigma-Aldrich

82100

Propylamine

assay

≥99.0% (GC)

assay

95%

assay

98%

assay

≥99.0% (GC)

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

density

0.787 g/mL at 25 °C (lit.)

density

0.787 g/mL at 25 °C (lit.)

density

0.806 g/mL at 25 °C (lit.)

density

0.719 g/mL at 25 °C (lit.)

refractive index

n20/D 1.436 (lit.)

refractive index

n20/D 1.436 (lit.)

refractive index

-

refractive index

n20/D 1.388 (lit.)

form

liquid

form

liquid

form

crystals

form

liquid

bp

216-218 °C (lit.)

bp

216-218 °C (lit.)

bp

247-249 °C (lit.)

bp

48 °C (lit.)

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].

signalword

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
BCCN3780
BCCN1533
BCCM5783
BCCL4674
BCCK6913

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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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