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77059

Sigma-Aldrich

Pentylamine

puriss., ≥99.5% (GC)

Synonym(s):

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
Beilstein:
505953
EC Number:
203-780-2
MDL number:
MFCD00008236
UNSPSC Code:
12352100
PubChem Substance ID:
24887117

vapor density

3.01 (vs air)

grade

puriss.

Assay

≥99.5% (GC)

expl. lim.

22 %

impurities

≤0.2% water

refractive index

n20/D 1.411 (lit.)
n20/D 1.412

bp

104 °C (lit.)

mp

−50 °C (lit.)

density

0.752 g/mL at 25 °C (lit.)

SMILES string

CCCCCN

InChI

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

InChI key

DPBLXKKOBLCELK-UHFFFAOYSA-N

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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

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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.
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
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
Paul Gee et al.
The New Zealand medical journal, 123(1327), 124-127 (2010-01-01)
"Party pills" continue to be legally sold though the main ingredient is no longer 1-benzylpiperazine. Dimethylamylamine (DMAA) is a synthetic stimulant and is one of the main ingredients of new "BZP-free party pills". Though patented in the 1950s as a
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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