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Perfiuoroisobutylene

CAS No.
382-21-8
Chemical Name:
Perfiuoroisobutylene
Synonyms
PFIB;Perfluoroisobutylene;PERFLUOROISOBUTENE;1,1,3,3,3-PENTAFLUORO-2-TRIFLUOROMETHYL-1-PROPENE;PERFLUORISOBUTYLENE;Perfiuoroisobutylene;Octafluoroisobutylene;Octafiuoroisobutylene;Perfluor-2-methylprop-1-ene;DAFIBNSJXIGBQB-UHFFFAOYSA-N
CBNumber:
CB5851872
Molecular Formula:
C4F8
Molecular Weight:
200.03
MDL Number:
MFCD00278866
MOL File:
382-21-8.mol
Last updated:2023-05-04 15:15:09

Perfiuoroisobutylene Properties

Melting point -130°C
Boiling point -3°C (estimate)
Density 1.5231 (rough estimate)
refractive index 1.2600 (estimate)
form A gas at room temp
FDA UNII 1J9BGS6NTY
EPA Substance Registry System 1-Propene, 1,1,3,3,3-pentafluoro-2-(trifluoromethyl)- (382-21-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS06
Signal word  Danger
Hazard statements  H330
Precautionary statements  P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501
RIDADR  3162
HazardClass  2.3
Toxicity LC50 ihl-rat: 500 ppb/6H 34ZIAG -,310,69

Perfiuoroisobutylene Chemical Properties,Uses,Production

Description

Perfluoroisobutylene (PFIB) is a schedule 2A substance under the Chemical Weapons Convention, which means that while it has significant ability to be used as a chemical weapon, it also serves various other industrial uses.

Uses

Perfluoroisobutylene or perfluoroisobutene is a monomer used in synthesis of Teflon and other polymeric materials. It is also used in etching for semiconductor fabrication, and is potentially used as a chemical warfare agent. The US Food and Drug Administration’s CFR 21 Section 173.360 allows for use of octafluorocyclobutane as a propellant and also allows for PFIB at a level of <.01% as an impurity in formulation.

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 2698, 1953 DOI: 10.1021/ja01107a044

Safety Profile

A deadly poison by inhalation. Askin, eye, and mucous membrane irritant. Human acuteexposure causes marked irritation of conjunctivae, throat,and lungs. When heated to decompos

Environmental Fate

PFIB exists as a gas in the atmosphere, and is degraded by reaction with hydroxyl radicals, with a reaction half-life of ~5.7 days. PFIB is not susceptible to significant photolysis. The Henry’s law constant of PFIB suggests volatization as an important fate process. The half lives for volatization calculated from a model lake and river were 5.6 days and 4.1 h, respectively, though a small portion will adsorb to suspended solids and sediment. PFIB can also volatize substantially from moist soils, and to a small degree from dry soils.

Toxicity evaluation

PFIB is a strong electrophile that reacts with nucleophiles. The toxicity of PFIB may be correlated with its susceptibility to nucleophilic attack and the generation of reactive intermediates.

75-46-7
115-25-3
116-14-3
116-15-4
382-21-8
Synthesis of Perfiuoroisobutylene from Trifluoromethane and Octafluorocyclobutane

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382-21-8(Perfiuoroisobutylene)Related Search:

Octafiuoroisobutylene Perfiuoroisobutylene Octafluoroisobutylene PERFLUORISOBUTYLENE Perfluor-2-methylprop-1-ene 2-(Trifluoromethyl)-1,1,3,3,3-pentafluoro-1-propene 2-Trifluoromethyl-1,1,3,3,3-pentafluoro-1-propene Octafluoroisobutene, in Nitrogen DAFIBNSJXIGBQB-UHFFFAOYSA-N 1-Propene, 1,1,3,3,3-pentafluoro-2-(trifluoromethyl)- Perfluoroisobutylene 1,1,3,3,3-PENTAFLUORO-2-TRIFLUOROMETHYL-1-PROPENE PERFLUOROISOBUTENE PFIB 382-21-8