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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:
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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Related Categories

Signal Word

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 Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

44.6 °F

Flash Point(C)

7 °C

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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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
Shawn P Vorce et al.
Journal of analytical toxicology, 35(3), 183-187 (2011-03-29)
The Department of Defense (DoD) operates six forensic urine drug-testing laboratories that screen close to 5 million urine samples for amphetamines yearly. Recently, the DoD laboratories have observed a significant decrease in the confirmation rates for amphetamines because of specimens
E Widy-Tyszkiewicz et al.
Pharmacology, biochemistry, and behavior, 13(3), 385-390 (1980-09-01)
Motor and autonomic effects of n-pentylamine in mice have been evaluated in relation to aminergic mechanisms by combining administration of the amine with drugs having well known effects on such mechanisms. Some evidence has been found to indicate the importance
Ju Hong Jeon et al.
FEBS letters, 534(1-3), 180-184 (2003-01-16)
Polyamine incorporation or cross-linking of proteins, post-translational modifications mediated by transglutaminase 2 (TGase 2), have been implicated in a variety of physiological functions including cell adhesion, extracellular matrix formation and apoptosis. To better understand the intracellular regulation mechanism of TGase
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
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