ChemicalBook > Product Catalog >Organic Chemistry >Amides >Acyclic polyamines and their derivatives >Isopropylamine

Isopropylamine

Isopropylamine Structure
CAS No.
75-31-0
Chemical Name:
Isopropylamine
Synonyms
MIPA;MONOISOPROPYLAMINE;2-Propanamine;2-Propylamine;Isopropylamine Anhydrous;sopropylamine;MIPA-70;nsc62775;iso-C3H7NH2;i-Propylamin
CBNumber:
CB8854223
Molecular Formula:
C3H9N
Molecular Weight:
59.11
MOL File:
75-31-0.mol
MSDS File:
SDS
Modify Date:
2024/5/23 18:06:45

Isopropylamine 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)
FEMA 4238 | ISOPROPYLAMINE
refractive index n20/D 1.374(lit.)
Flash point −26 °F
storage temp. 2-8°C
solubility 1000g/l
form Crystalline Powder, Needles or Crystals
pka 10.63(at 25℃)
color APHA: ≤50
Odor Strong ammoniacal; pungent, irritating, typical amine.
PH 13 (700g/l, H2O, 20℃)
explosive limit 2-10.4%(V)
Odor Threshold 0.025ppm
Odor Type fishy
Water Solubility soluble
Sensitive Air Sensitive
JECFA Number 1581
Merck 14,5209
BRN 605259
Exposure limits TLV-TWA 5 ppm (~12 mg/m3) (ACGIH, MSHA, and OSHA); TLV-STEL 10 ppm(~24 mg/m3) (ACGIH); IDLH 4000 ppm (NIOSH).
Dielectric constant 5.5(20℃)
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.
LogP 0.21
CAS DataBase Reference 75-31-0(CAS DataBase Reference)
NIST Chemistry Reference 2-Propanamine(75-31-0)
EPA Substance Registry System Isopropylamine (75-31-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS05,GHS06
Signal word  Danger
Hazard statements  H224-H301+H311+H331-H314-H335
Precautionary statements  P210-P233-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P403+P233
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
34
Autoignition Temperature 755 °F
TSCA  Yes
HS Code  2921 19 99
HazardClass  3
PackingGroup  I
Toxicity LD50 orally in rats: 820 mg/kg (Smyth)
IDLA 750 ppm
NFPA 704
4
3 0

Isopropylamine price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 8.07476 Isopropylamine for synthesis 75-31-0 100ML ₹4480 2022-06-14 Buy
Sigma-Aldrich(India) 8.07476 Isopropylamine for synthesis 75-31-0 1L ₹9019.99 2022-06-14 Buy
Sigma-Aldrich(India) 8.07476 Isopropylamine for synthesis 75-31-0 2.5L ₹10230.01 2022-06-14 Buy
Sigma-Aldrich(India) 471291 Isopropylamine ≥99.5% 75-31-0 25ML ₹2987.7 2022-06-14 Buy
Sigma-Aldrich(India) 59330 Isopropylamine ≥97.0% (GC) 75-31-0 1L ₹3431.53 2022-06-14 Buy
Product number Packaging Price Buy
8.07476 100ML ₹4480 Buy
8.07476 1L ₹9019.99 Buy
8.07476 2.5L ₹10230.01 Buy
471291 25ML ₹2987.7 Buy
59330 1L ₹3431.53 Buy

Isopropylamine Chemical Properties,Uses,Production

Description

Isopropylamine (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 Properties

Isopropylamine 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 properties

Colorless 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).

Occurrence

Not reported found in natu

Uses

Isopropylamine is used as a dehairing agentand as an intermediate in the preparation ofmany organics.

Uses

Isopropylamine 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. such as bentazon (BASF), Roundup (Monsanto), imazapyr (ACC) and the triazines ametryne (Novartis), atrazine (Novartis), desmetryn (Novartis), prometryn (Novartis), pramitol (Novartis), dipropetryn (Novartis), and propazine. Other applications encompass the nematicide fenamiphos (Bayer), the fungicide iprodione (Rho?ne-Poulenc), insecticides, pharmaceuticals, and surfactants.

Production Methods

Isopropylamine 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).

Definition

ChEBI: A member of the class of alkylamines that is propane carrying an amino group at position 2.

General Description

A 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 Reactions

Highly flammable. Water soluble.

Reactivity Profile

Isopropylamine 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].

Hazard

Highly flammable, dangerous fire risk. Strong irritant to tissue.

Health Hazard

Isopropylamine 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 Reactivity

Reactivity 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 uses

Isopropylamine 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 Fate

Photolytic. 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.

Metabolism

One 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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