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Merck
CN

W424201

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
NACRES:
NA.21
PubChem Substance ID:
24901991
UNSPSC Code:
12164502
FEMA Number:
4242
Flavis number:
11.021
EC Number:
203-780-2
MDL number:
MFCD00008236
Beilstein/REAXYS Number:
505953
Organoleptic:
fishy
Grade:
FG
Biological source:
synthetic
Food allergen:
no known allergens

Key Documents

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Product Name

Amylamine, ≥99%, FG

InChI

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

InChI key

DPBLXKKOBLCELK-UHFFFAOYSA-N

SMILES string

CCCCCN

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

Quality Level

300

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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

WGK 1

flash_point_f

44.6 °F

flash_point_c

7 °C

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SHBT1777
SHBP6763
STBJ4046
STBH0557
STBG7380

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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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