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About This Item
Linear Formula:
CH3(CH2)4NH2
CAS Number:
Molecular Weight:
87.16
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
4242
Flavis number:
11.021
EC Number:
203-780-2
MDL number:
Beilstein/REAXYS Number:
505953
Organoleptic:
fishy
Grade:
FG
Biological source:
synthetic
Food allergen:
no known allergens
biological source
synthetic
Quality Level
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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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
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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
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
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


