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W424201

Sigma-Aldrich

Amylamine

≥99%, FG

Synonym(s):

Pentylamine, 1-Aminopentane, n-Amylamine

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About This Item

Linear Formula:
CH3(CH2)4NH2
CAS Number:
110-58-7
Molecular Weight:
87.16
FEMA Number:
4242
Beilstein/REAXYS Number:
505953
EC Number:
203-780-2
MDL number:
MFCD00008236
UNSPSC Code:
12164502
PubChem Substance ID:
24901991
Flavis number:
11.021
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG

reg. compliance

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR part 172.515

vapor density

3.01 (vs air)

assay

≥99%

expl. lim.

22 %

refractive index

n20/D 1.411 (lit.)

bp

104 °C (lit.)

mp

−50 °C (lit.)

density

0.752 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

fishy

SMILES string

CCCCCN

InChI

1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3

InChI key

DPBLXKKOBLCELK-UHFFFAOYSA-N

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Related Categories

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

44.6 °F

flash_point_c

7 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ4046
STBH0557
STBG7380
S87725V
S89325V

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V V Novokhatny et al.
Thrombosis research, 53(3), 243-252 (1989-02-01)
The interaction of the isolated kringles 4 and 5 from human plasminogen with 6-aminohexanoic acid, pentylamine, pentanoic acid and arginine has been quantitatively characterized by scanning calorimetry and fluorescent spectroscopy. It has been found that the ligands with the positively
C Guffroy et al.
The Journal of pharmacy and pharmacology, 35(7), 416-420 (1983-07-01)
n-Pentylamine is deaminated by homogenates of rat heart. Clorgyline inhibition curves at 10 and 100 microM n-pentylamine indicated that this substrate was deaminated by MAO-A, -B and a clorgyline-resistant amine oxidase sensitive to inhibition by semicarbazide. These results have been
Zan Xie et al.
Journal of chromatography. A, 1104(1-2), 173-178 (2005-12-27)
Volatile organic amine was used as the mobile phase addictive during the separation of four bisphosphonates (alendronate, pamidronate, zoledronic acid and etidronate). An isocratic liquid chromatography method with evaporative light-scattering detection (ELSD) was developed for these bisphosphonates which are not
Y V Matsuka et al.
European journal of biochemistry, 190(1), 93-97 (1990-05-31)
The ligand binding of kringle 1 + 2 + 3 and kringle 1 from human plasminogen has been investigated by fluorescence spectroscopy. Analysis of fluorescence titration of kringle 1 + 2 + 3 with 6-aminohexanoic acid shows that this fragment
J G Liehr et al.
Carcinogenesis, 6(6), 829-836 (1985-06-01)
In a search for the carcinogenic metabolite of diethylstilbestrol, the interactions of 4',4"-diethylstilbestrol quinone with peptides and nucleic acids were investigated. Nonextractable binding of 4',4"-diethylstilbestrol quinone to calf thymus DNA or poly G were observed. However, adduct nucleosides could not
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Protocols

GC Analysis of Primary Amines on Carbowax® Amine

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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