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Isopropylamine Suppliers list
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: 0371-55170693
Products Intro: Product Name:75-31-0
Purity:0.99 Package:25KG,5KG;1KG;500G
Tel: +86 18953170293
Products Intro: Product Name:isopropylamine
Purity:0.99 Package:5KG;1KG
Company Name: Hubei Jusheng Technology Co.,Ltd.
Tel: 86-18871470254
Products Intro: Product Name:isopropylamine
Purity:99% Package:5KG;1KG
Company Name: Hebei Guanlang Biotechnology Co., Ltd.
Tel: +8619930503282
Products Intro: Product Name:Isopropylamine
Purity:99% Package:1KG;1USD
Company Name: Xiamen AmoyChem Co., Ltd
Tel: +86 592-605 1114
Products Intro: Product Name:Isopropylamine

Isopropylamine manufacturers

  • Isopropylamine
  • $20.00 / Kg/Drum
  • 2022-01-21
  • CAS:75-31-0
  • Min. Order: 25Kg/Drum
  • Purity: 99.99%
  • Supply Ability: 1 ton per week
  • Isopropylamine
  • $5.00 / KG
  • 2021-11-08
  • CAS:75-31-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20 Tons
  • 2-nitroimidazole
  • $12.00 / KG
  • 2020-08-27
  • CAS:75-31-0
  • Min. Order: 1KG
  • Purity: 99%min
  • Supply Ability: 5000 Kilogram/Kilograms per Month
Isopropylamine Basic information
Product Name:Isopropylamine
Synonyms:iso-C3H7NH2;Isopropilamina;Isopropylamin;iso-Propylamine gas;isopropylamine(2-aminopropane);isopropylamine(non-specificname);isopropylaminemethylnaphthalenesulfonate;nsc62775
Product Categories:HPLC and LCMS Mobile Phase Additive
Mol File:75-31-0.mol
Isopropylamine Structure
Isopropylamine Chemical Properties
Melting point -101 °C
Boiling point 32-35 °C 33-34 °C (lit.)
density 0.688 g/mL at 20 °C (lit.)
vapor density 2.04 (vs air)
vapor pressure 9.2 psi ( 20 °C)
refractive index n20/D 1.374(lit.)
Fp −26 °F
storage temp. 2-8°C
solubility 1000g/l
form Crystalline Powder, Needles or Crystals
pka10.63(at 25℃)
color APHA: ≤50
PH13 (700g/l, H2O, 20℃)
OdorStrong ammoniacal; pungent, irritating, typical amine.
Odor Threshold0.025ppm
explosive limit2-10.4%(V)
Water Solubility soluble
Sensitive Air Sensitive
JECFA Number1581
Merck 14,5209
BRN 605259
Exposure limitsTLV-TWA 5 ppm (~12 mg/m3) (ACGIH, MSHA, and OSHA); TLV-STEL 10 ppm(~24 mg/m3) (ACGIH); IDLH 4000 ppm (NIOSH).
Stability:Stable. Extremely flammable - note low boiling point and low flash point. Readily forms explosive mixtures with air. Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides, perchloryl fluoride.
CAS DataBase Reference75-31-0(CAS DataBase Reference)
NIST Chemistry Reference2-Propanamine(75-31-0)
EPA Substance Registry SystemIsopropylamine (75-31-0)
Safety Information
Hazard Codes F+,Xi,T
Risk Statements 12-36/37/38-37-35-25-20/21
Safety Statements 16-26-29-45-36/37/39
RIDADR UN 1221 3/PG 1
WGK Germany 1
RTECS NT8400000
Autoignition Temperature755 °F
HS Code 2921 19 99
HazardClass 3
PackingGroup I
Hazardous Substances Data75-31-0(Hazardous Substances Data)
ToxicityLD50 orally in rats: 820 mg/kg (Smyth)
MSDS Information
ACROS English
SigmaAldrich English
ALFA English
Isopropylamine Usage And Synthesis
DescriptionIsopropylamine (propan-2-amine, IUPAC) is a colorless, volatile liquid. It is highly flammable, with a flammable range of 2%–10.4% in air. Boiling point is 93°F (33°C), flash point is ?15°F (?26°C), and ignition temperature is 756°F (402°C).
It is miscible with water, with a specific gravity of 0.69, which is lighter than water. Vapor density is 2.04, which is heavier than air. In addition to flammability, isopropylamine is a strong irritant to tissue and has a TLV of 5 ppm in air. The four-digit UN identification number is 1221. The NFPA 704 designation for isopropylamine is health 3, flammability 4, and reactivity 0. Primary uses for isopropylamine are pharmaceuticals, dyes, insecticides, and as a dehairing agent.
Chemical PropertiesIsopropylamine is a colorless, flammable liquid. Isopropylamine is miscible with water, alcohol, and ether.The odor threshold reportedly ranges from 0.21 to 0.70 ppm; the pungent, ammoniacal odor becomes irritating at 24mg/m3 (110).
Physical propertiesColorless liquid with a penetrating, ammonia-like odor. Experimentally determined detection and recognition odor threshold concentrations were 500 μg/m3 (210 ppbv) and 1.7 mg/m3 (700 ppbv), respectively (Hellman and Small, 1974). An odor threshold concentration of 25 ppbv was reported by Nagata and Takeuchi (1990).
OccurrenceNot reported found in natu
UsesIsopropylamine is used as a dehairing agentand as an intermediate in the preparation ofmany organics.
UsesIsopropylamine is an organic compound is a widely used for the synthesis of pharmaceutical and agricultural goods such as glyphosphate herbicides and as an additive for petroleum industry.
UsesSolvent, intermediate in synthesis of rubber accelerators, pharmaceuticals, dyes, insecticides, bactericides, textile specialties, and surface-active agents, dehairing agent, solubilizer for 2,4-D acid.
Production MethodsIsopropylamine can be produced from the corresponding alcohol by reacting with ammonia in the presence of a dehydrating catalyst, or from the chloride by reacting with ammonia under pressure. It is also reported that this amine can be produced from acetone and ammonia or from the acetone oxime (HSDB 1989).
DefinitionChEBI: A member of the class of alkylamines that is propane carrying an amino group at position 2.
Aroma threshold valuesHigh strength odor; fishy type; recommend smelling in a 0.10% solution or less.
General DescriptionA clear colorless liquid with an ammonia-like odor. Flash point -35°F. Boiling point 90°F. Less dense than water Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Used as a solvent and to make other chemicals.
Air & Water ReactionsHighly flammable. Water soluble.
Reactivity ProfileIsopropylamine is a colorless, alkaline liquid, very volatile, moderately toxic, highly flammable. Dangerous fire hazard when exposed to heat, flame, sparks, or strong oxidizers. When heated to decomposition Isopropylamine emits toxic fumes of oxides of nitrogen [M. K.]. A mixture of Isopropylamine and perchloryl fluoride resulted in an uncontrolled oxidation and/or explosion, [J. Org. Chem., 1980, 45, 4036]. The reaction of 1-chloro-2,3-epoxypropane and the amine and most probably other nitrogen bases, yields a violent exotherm, [Chem. & Ind., 1971, 994].
HazardHighly flammable, dangerous fire risk. Strong irritant to tissue.
Health HazardIsopropylamine is a strong irritant to theeyes, skin, and respiratory system. A shortexposure to 10–20 ppm can cause irritationof the nose and throat in humans (Procturand Hughes 1978). Prolonged exposure tohigh concentrations may lead to pulmonaryedema. Skin contact can cause dermatitisand skin burns. Exposure to 8000 ppm for4 hours was lethal to rats.
LD50 value, oral (mice): 2200 mg/kg.
Chemical ReactivityReactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Industrial usesIsopropylamine can be used as a dehairing agent and as a solvent. It also finds use as an intermediate in the production of insecticides, herbicides and bactericides and in the production of pharmaceuticals, dyes and rubber accelerators (HSDB 1989).
Environmental fatePhotolytic. Low et al. (1991) reported that the photooxidation of aqueous primary amine solutions by UV light in the presence of titanium dioxide resulted in the formation of ammonium and nitrate ions.
Chemical/Physical. Releases toxic nitrogen oxides when heated to decomposition (Sax and Lewis, 1987). Forms water-soluble salts with acids.
MetabolismOne would expect isopropylamine to be readily absorbed from the gut and respiratory tract. Shorter chain aliphatic amines such as isopropylamine also are efficiently absorbed through the skin (Beard and Noe 1981). When administered intravenously, isopropylamine distributed rapidly into tissue compartments with tissue/plasma ratios ranging from 1.8 in the atrium to 16.7 in the renal medulla (Privitera et al 1982). During the elimination phase, a half-life of 146 min was observed in plasma. There do not appear to be any definitive metabolic studies with this compound, however through a comparison with other substrates, one might expect oxidation to acetone and ammonia through the action of monoamine oxidase (Tipton 1980).
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