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Merck
CN

442540

Supelco

Decylamine

analytical standard

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:
12352200
PubChem Substance ID:
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grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

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.)

application(s)

environmental

format

neat

storage temp.

2-30°C

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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General description

Decylamine is a hydrophobic long alkylated cationic ammonium that is used to modify the polarity of reversed phases on octadecylsilyl (ODS) gels.

Application

Decylamine is used as a pairing agent to enhance the retention of ascorbic acid isomers on a C18 column during the analysis of the isomers in fortified food products by high performance liquid chromatography (HPLC).
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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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Certificates of Analysis (COA)

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Determination of theophylline and its metabolites in plasma and urine by reversed-phase liquid chromatography using an amine modifier
Naline E, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 419, 177-189 (1987)
HPLC-UV determination of total vitamin C in a wide range of fortified food products
Fontannaz P, et al.
Food Chemistry, 94(4), 626-631 (2006)
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
Monika Naumowicz et al.
Cell biochemistry and biophysics, 61(1), 145-155 (2011-02-23)
Bilayer lipid membranes composed of phosphatidylcholine and decanoic acid or phosphatidylcholine and decylamine were investigated using electrochemical impedance spectroscopy. Interaction between membrane components causes significant deviations from the additivity rule. Area, capacitance, and stability constant values for the complexes were

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