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30692

Sigma-Aldrich

Decylamine

≥99.0% (GC)

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Synonym(s):
1-Aminodecane, NDA
Linear Formula:
CH3(CH2)9NH2
CAS Number:
Molecular Weight:
157.30
Beilstein:
1735220
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

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.)

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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1 of 4

This Item
D22220882100219703
Decylamine ≥99.0% (GC)

Sigma-Aldrich

30692

Decylamine

Dodecylamine 98%

Sigma-Aldrich

D222208

Dodecylamine

Propylamine purum, ≥99.0% (GC)

Sigma-Aldrich

82100

Propylamine

Hexylamine 99%

Sigma-Aldrich

219703

Hexylamine

form

liquid

form

crystals

form

liquid

form

liquid

refractive index

n20/D 1.436 (lit.)

refractive index

-

refractive index

n20/D 1.388 (lit.)

refractive index

n20/D 1.418 (lit.)

bp

216-218 °C (lit.)

bp

247-249 °C (lit.)

bp

48 °C (lit.)

bp

131-132 °C (lit.)

mp

12-14 °C (lit.)

mp

27-29 °C (lit.)

mp

−83 °C (lit.)

mp

−23 °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.)

density

0.766 g/mL at 25 °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. It was also used as a coordinating solvent to thermolyse the lead piperidine and lead tetrahydroquinoline dithiocarbamate (DTC) complexes.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

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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
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
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.
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

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