Pentylamine
Names | |
---|---|
Preferred IUPAC name
Pentanamine | |
Systematic IUPAC name
Pentan-1-amine[1] | |
Other names
| |
Identifiers | |
110-58-7 | |
505953 | |
ChEBI | CHEBI:74848 |
ChemSpider | 7769 |
DrugBank | DB02045 |
EC Number | 203-780-2 |
Jmol interactive 3D | Image |
MeSH | n-amylamine |
PubChem | 8060 |
RTECS number | SC0300000 |
UN number | 1106 |
| |
| |
Properties | |
C5H13N | |
Molar mass | 87.17 g·mol−1 |
Appearance | Colourless liquid |
Density | 0.752 g mL−1 |
Melting point | −55 °C; −67 °F; 218 K |
Boiling point | 94 to 110 °C; 201 to 230 °F; 367 to 383 K |
Miscible | |
Henry's law constant (kH) |
410 μmol Pa−1 kg−1 |
Refractive index (nD) |
1.411 |
Thermochemistry | |
218 J K−1 mol−1 (at −75 °C) | |
Hazards | |
GHS pictograms | |
GHS signal word | DANGER |
H225, H302, H312, H314, H331 | |
P210, P261, P280, P305+351+338, P310 | |
EU classification (DSD) |
F C |
R-phrases | R11, R20/21/22, R34 |
S-phrases | S16, S26, S33, S36/37/39, S45 |
Flash point | 1 °C (34 °F; 274 K) |
Explosive limits | 2.2–22% |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose) |
|
Related compounds | |
Related alkanamines |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
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,[2] and as a flavoring agent.[3]
References
- ↑ "n-amylamine - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 26 May 2012.
- ↑ Flick, Ernest W. (1998). Industrial Solvents Handbook (5th ed.). Park Ridge, NJ: William Andrew. p. 695. ISBN 0-8155-1413-1.
- ↑ "JECFA Evaluations-PENTYLAMINE. Summary of Evaluations Performed by the Joint FAO/WHO Expert Committee on Food Additives" (January 31, 2006). Retrieved on 2008-07-25
This article is issued from Wikipedia - version of the Thursday, August 06, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.