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W424201

Sigma-Aldrich

Amylamine

≥99%, FG

Sinónimos:

Pentylamine, 1-Aminopentane, n-Amylamine

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About This Item

Fórmula lineal:
CH3(CH2)4NH2
Número de CAS:
110-58-7
Peso molecular:
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

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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Categorías relacionadas

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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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
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
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
E Widy-Tyszkiewicz et al.
Polish journal of pharmacology and pharmacy, 35(6), 467-472 (1983-11-01)
The effect of butylamine, pentylamine and hexylamine on spontaneous locomotor activity of mice was evaluated in the presence or absence of drugs affecting monoaminergic neurons. Pentylamine and hexylamine produced similar effects (stimulation after low, inhibition after high doses), while butylamine
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