Weight | 87.166 g/mol |
---|---|
Formula | C5H13N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Amylamine (110-58-7)
amylamine hydrochloride · n-amylamine · n-amylamine hydrochloride
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- Amylamine stabilized platinum(0) nanoparticles: active and reusable nanocatalyst in the room temperature dehydrogenation of dimethylamine-borane (RSC Advances, 2014)
- Simple analysis of four bisphosphonates simultaneously by reverse phase liquid chromatography using n-amylamine as volatile ion-pairing agent (Journal of Chromatography A, 2006)
- Mechanism of carbon-nitrogen bond cleavage during amylamine hydrodenitrogenation over a sulphided NiMo/Al2O3 catalyst (Catalysis Letters, 1991)
- Kinetic Studies of Fast Reactions in Aqueous Solutions of Amylamine by Means of Ultrasonic Absorption (Bulletin of the Chemical Society of Japan, 1973)
- Formation of Hydroxy Derivatives, Aldehydes, and Nitrite from N-Nitrosomethyl-n-amylamine by Rat Liver Microsomes and by Purified Cytochrome P-450 IIB1 (Cancer Research, 1989)
- Pure compound and cross second virial coefficients for n-amylaminealcohol systems at 363.15 K. Measurements with a low pressure Burnett-type apparatus (Fluid Phase Equilibria, 1989)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - amylamine hydrochloride
- n-amylamine
- n-amylamine hydrochloride
- n-amylamine sulfate (2:1)
- n-pentylamine
-
SMILESCCCCCN
-
InChIKeyDPBLXKKOBLCELK-UHFFFAOYSA-N
- Pubchem - Amylamine
- Wikipedia - pentylamine
Pentylamine is a chemical compound with the formula CH3(CH2)4NH2. It is used as a solvent, as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers, and pharmaceutical products, and as a flavoring agent. Pentylamine exhibits reactions typical of other simple alkyl amines, i.e.
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