Isopropylamine

Isopropylamine (monoisopropyl amine, MIPA, 2-Propylamine) is an organic compound, an amine. It is a hygroscopic colorless liquid with ammonia-like odor. It is miscible with water and flammable. It is a valuable intermediate in chemical industry.[3]

Isopropylamine
Skeletal formula of isopropylamine
Ball-and-stick model of the isopropylamine molecule
Names
Preferred IUPAC name
Propan-2-amine
Other names
  • (Propan-2-yl)amine
  • Isopropylamine
  • 2-aminopropane
  • 2-propanamine
  • monoisopropylamine
  • MIPA
Identifiers
3D model (JSmol)
3DMet
605259
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.783
EC Number
  • 200-860-9
KEGG
MeSH 2-propylamine
RTECS number
  • NT8400000
UNII
UN number 1221
Properties
C3H9N
Molar mass 59.112 g·mol−1
Appearance Colourless liquid
Odor "Fishy"; ammoniacal
Density 688 mg mL−1
Melting point −95.20 °C; −139.36 °F; 177.95 K
Boiling point 31 to 35 °C; 88 to 95 °F; 304 to 308 K
Miscible
log P 0.391
Vapor pressure 63.41 kPa (at 20 °C)
1.3742
Thermochemistry
163.85 J K−1 mol−1
218.32 J K−1 mol−1
Std enthalpy of
formation (ΔfH⦵298)
 −113.0–−111.6 kJ mol−1
Std enthalpy of
combustion (ΔcH⦵298)
 −2.3540–−2.3550 MJ mol−1
Hazards
GHS pictograms
GHS Signal word Danger
GHS hazard statements
 H224, H315, H319, H335
P210, P261, P305+351+338
Flash point −18 °C (0 °F; 255 K)
402 °C (756 °F; 675 K)
Explosive limits 2–10.4%
Lethal dose or concentration (LD, LC):
  • 380 mg kg−1 (dermal, rabbit)
  • 550 mg kg−1 (oral, rat)
4,000 ppm (rat, 4 hr)[1]
7000 ppm (mouse, 40 min)[1]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 5 ppm (12 mg/m3)[2]
REL (Recommended)
 None established[2]
IDLH (Immediate danger)
 750 ppm[2]
Related compounds
Related alkanamines
Related compounds
 2-Methyl-2-nitrosopropane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Reactions

Isopropylamine exhibits reactions typical of other simple alkyl amines, i.e. protonation, alkylation, acylation, condensation with carbonyls. Like other simple aliphatic amines, isopropylamine is a weak base: the pKa of [(CH3)2)CHNH3]+ is 10.63.[4]

Preparation and use

Isopropylamine can be obtained by aminating isopropyl alcohol with ammonia in presence of a catalyst:[3]

(CH3)2CHOH + NH3 → (CH3)2CHNH2 + H2O

Isopropylamine is a building block for the preparation of many herbicides and pesticides including atrazine, bentazon, glyphosate, imazapyr, ametryne, desmetryn, prometryn, pramitol, dipropetryn, propazine, fenamiphos, and iprodione.[3] It is a regulating agent for plastics, intermediate in organic synthesis of coating materials, plastics, pesticides, rubber chemicals, pharmaceuticals and others, and as an additive in the petroleum industry.

References
  1. "Isopropylamine". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health. 4 December 2014. Retrieved 14 April 2015.
  2. NIOSH Pocket Guide to Chemical Hazards. "#0360". National Institute for Occupational Safety and Health (NIOSH).
  3. Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a02_001
  4. H. K. Hall, Jr. (1957). "Correlation of the Base Strengths of Amines". J. Am. Chem. Soc. 79: 5441–5444. doi:10.1021/ja01577a030.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.