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W424201

Sigma-Aldrich

Amylamin

≥99%, FG

Synonym(e):

Pentylamin, 1-Amino-pentan, n-Amylamin

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About This Item

Lineare Formel:
CH3(CH2)4NH2
CAS-Nummer:
110-58-7
Molekulargewicht:
87.16
FEMA-Nummer:
4242
Beilstein:
505953
EG-Nummer:
203-780-2
MDL-Nummer:
MFCD00008236
UNSPSC-Code:
12164502
PubChem Substanz-ID:
24901991
Flavis-Nummer:
11.021
NACRES:
NA.21

Biologische Quelle

synthetic

Qualität

FG

Einhaltung gesetzlicher Vorschriften

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

Dampfdichte

3.01 (vs air)

Assay

≥99%

Expl.-Gr.

22 %

Brechungsindex

n20/D 1.411 (lit.)

bp

104 °C (lit.)

mp (Schmelzpunkt)

−50 °C (lit.)

Dichte

0.752 g/mL at 25 °C (lit.)

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Organoleptisch

fishy

SMILES String

CCCCCN

InChI

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

InChIKey

DPBLXKKOBLCELK-UHFFFAOYSA-N

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Verwandte Kategorien

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

44.6 °F

Flammpunkt (°C)

7 °C

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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.
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
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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