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382-21-8

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382-21-8 Usage

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.

Check Digit Verification of cas no

The CAS Registry Mumber 382-21-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 382-21:
(5*3)+(4*8)+(3*2)+(2*2)+(1*1)=58
58 % 10 = 8
So 382-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C4F8/c5-2(6)1(3(7,8)9)4(10,11)12

382-21-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3,3-pentafluoro-2-(trifluoromethyl)prop-1-ene

1.2 Other means of identification

Product number -
Other names Octafluoroisobutylene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:382-21-8 SDS

382-21-8Relevant articles and documents

Gregory et al.

, p. 991 (1969)

Generation of Perfluoroisobutylene Reference Sample and Determination by Gas Chromatography with Electron Capture and Flame Ionization Detection

Marhevka, John S.,Johnson, Glenn D.,Hagen, Donald F.,Danielson, Richard D.

, p. 2607 - 2610 (1982)

-

IR Matrix Isolation Product Characterization from Low-Pressure Pyrolysis of CnF2n+1I (n = 1-4) and C6F5I

Butler, R.,Snelson, A.

, p. 345 - 350 (1980)

-

Synthesis of 3,3,3-trifluoroethyl isocyanate, carbamate and ureas. Anticancer activity evaluation of N-(3,3,3-trifluoroethyl)-N′-substituted ureas

Luzina, Elena L.,Popov, Anatoliy V.

, p. 82 - 88 (2015/06/25)

A new method is described for producing 3,3,3-trifluoroethyl isocyanate from perfluoroisobutene (PFIB). Isocyanate was used for synthesis of carbamates and ureas. A series of trifluoroethyl-substituted ureas has been tested in the National Cancer Institute (NCI, Bethesda, USA) by the NCI-60 DTP Human Tumor Cell Line Screening Program at a single high dose (10-5 M). The moderate anticancer activity was shown against some types of cancer on the individual human cell lines for leukemia, non-small cell lung cancer and renal cancer.

PYROLYSIS PROCESS

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Page/Page column 4, (2008/06/13)

The present invention relates to the pyrolysis of hydrochlorofluorocarbons to form fluoromonomers such as tetrafluoroethylene, the pyrolysis being carried out in a reaction zone lined with nickel and mechanically supported by a jacket of other corrosion resistant metal, the nickel lining providing an improved yield of valuable reaction products.

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