126810 is for lab research only, not for any medication.
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126810
Isopentylamin
99%
Synonym(e):
Isoamylamin, Isopentylamin
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10 G
CHF 37.60
100 G
CHF 184.00
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10 G
CHF 37.60
100 G
CHF 184.00
About This Item
Lineare Formel:
(CH3)2CHCH2CH2NH2
CAS-Nummer:
Molekulargewicht:
87.16
Beilstein:
1209230
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Assay
99%
Form
liquid
Brechungsindex
n20/D 1.408 (lit.)
bp
95-97 °C (lit.)
Dichte
0.751 g/mL at 25 °C (lit.)
Funktionelle Gruppe
amine
SMILES String
CC(C)CCN
InChI
1S/C5H13N/c1-5(2)3-4-6/h5H,3-4,6H2,1-2H3
InChIKey
BMFVGAAISNGQNM-UHFFFAOYSA-N
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Verwandte Kategorien
Signalwort
Danger
Gefahreneinstufungen
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 1
Flammpunkt (°F)
30.2 °F - closed cup
Flammpunkt (°C)
-1 °C - closed cup
Persönliche Schutzausrüstung
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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S E Atawodi et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 33(8), 625-630 (1995-08-01)
Three varieties of kola nut, Cola acuminata, C. nitida and Garcinia cola, of Nigerian origin, were analysed for their content of primary and secondary amines, and assessed for their relative methylating potential due to nitrosamide formation. Primary and secondary amines
L Larsson et al.
Acta pathologica et microbiologica Scandinavica. Section B, Microbiology, 86(4), 207-213 (1978-08-01)
A gas chromatographic (GC) head-space technique is presented, which is suitable for the analysis of volatile products in bacterial broth cultures. This is exemplified by studies on Clostridium septicum, Klebsiella pneumoniae and Proteus mirabilis. The media were acidified or made
The deamination of isoamylamine by monamine oxidase in mitochondrial preparations from rat liver and heart: a comparison with phenylethylamine.
E M Peers et al.
Biochemical pharmacology, 29(8), 1097-1102 (1980-04-15)
[Studies on the synthesis of two new nitrosamines (NMAMBA and NMAMPA) from isoamylamine and sodium nitrite by fungi].
S J Lu et al.
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae, 8(4), 255-260 (1986-08-01)
C Ji et al.
Carcinogenesis, 7(2), 301-303 (1986-02-01)
Nitrosomethylisoamylamine (NMIA), a carcinogenic N-nitroso compound was synthesized from isoamylamine (IAA) in a glucose-ammonium nitrate medium after several days' incubation with fungi and subsequent nitrosation with sodium nitrate. The nitrosamine was not produced by control reactions which lacked either IAA
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