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30692

Sigma-Aldrich

Decylamine

≥99.0% (GC)

Sinónimos:

1-Aminodecane, NDA

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About This Item

Fórmula lineal:
CH3(CH2)9NH2
Número de CAS:
2016-57-1
Peso molecular:
157.30
Beilstein/REAXYS Number:
1735220
EC Number:
217-957-7
MDL number:
MFCD00008149
UNSPSC Code:
12352100
PubChem Substance ID:
57648462
NACRES:
NA.22

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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Categorías relacionadas

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.

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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Certificados de análisis (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
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.
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