Isopropylamine manufacturers and suppliers in india

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

PH: 13 (700g/l, H2O, 20℃)

Odor: Strong ammoniacal; pungent, irritating, typical amine.

Odor Threshold: 0.025ppm

explosive limit: 2-10.4%(V)

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

Safety Information

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

F: 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

Use

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).