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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:
Molecular Weight:
157.30
Beilstein:
1735220
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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 Naline et al.
Journal of chromatography, 419, 177-189 (1987-08-07)
A high-performance liquid chromatographic method for the determination of the concentrations of theophylline and its metabolites in plasma and urine samples is presented. The method uses the decylammonium ion, an N-alkylammonium modifier, and makes it possible to separate theophylline and

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