Ethyl Corp

Atochem, France (EA) Ethyl Corp., United States (EC) Great Lakes, United States (GL) ISC Chemicals, Ltd. United Kingdom (ISC) Manac Inc., Japan (MI) Mambishi, Japan (M) Mitsui Toatsu Fiae Chemicals, Inc., Japan (MT) Nippon Chemicals Corp., Ltd., Japan (NC) Teijia, Japan (T) Tosoh, Japan (TS) Warwick International, United Kingdom (WI) CECA, SA, France (CECA). 

Material safety data sheets from Ethyl Corp. (EC) and Great Lakes (GL). Product data sheet from Dead Sea Bromine. 

The Brominated Flame Retardants Industry Panel (BFRIP) was formed ia 1985 within the Flame Retardant Chemicals Association (FRCA) to address such concerns about the use of decabromodiphenyl oxide. Siace 1990 the BFRIP has operated as a Chemical Self-Funded Technical Advocacy and Research (CHEMSTAR) panel within the Chemical Manufacturers Association (CMA) (64). As of 1993, members of BFRIP are Ak2o, Amerihaas (Dead Sea Bromine Group), Ethyl Corp., and Great Lakes Chemical. Siace its formation, BFRIP has presented updates to iadustry on a regular basis (65,66), and has pubhshed a summary of the available toxicity information on four of the largest volume brominated flame retardants (67,68) tetrabromo bisphenol A, pentabromodiphenyl oxide, octabromodiphenyl oxide, and decabromodiphenyl oxide. This information supplements that summarized ia Table 11. 

SAYTEX 102E Flame Retardant Product Bulletin, Ethyl Corp., Baton Rouge, La., 1992. 

In 1957, Ethyl Corp. announced anew antiknock compound, methylcyclopentadienyknanganese tricarbonyl [12108-13-3] (MMT). MMT is almost as effective as lead on a per gram of metal basis, but because manganese was more expensive than lead, MMT was not widely used until limits were placed on the lead content of gasoline. MMT was used in unleaded fuel between 1975 and 1978. After a large fleet test suggested that MMT could increase exhaust emissions because it interfered with catalysts and oxygen sensors, EPA banned its use in unleaded fuel in 1978. MMT is used in Canada in unleaded fuel. 

Applications. Among the P—O- and P—N-substituted polymers, the fluoroalkoxy- and aryloxy-substituted polymers have so far shown the greatest commercial promise (14—16). Both poly[bis(2,2,2-trifluoroethoxy)phosphazene] [27290-40-0] and poly(diphenoxyphosphazene) [28212-48-8] are microcrystalline, thermoplastic polymers. However, when the substituent symmetry is dismpted with a randomly placed second substituent of different length, the polymers become amorphous and serve as good elastomers. Following initial development of the fluorophosphazene elastomers by the Firestone Tire and Rubber Co., both the fluoroalkoxy (EYPEL-F) and aryloxy (EYPEL-A) elastomers were manufactured by the Ethyl Corp. in the United States from the mid-1980s until 1993 (see ELASTOLffiRS,SYNTHETic-PHOSPHAZENEs). 

Monophenols 2,6-di- / l -butylphenol [128-39-2] C14H22O F, GAS, PO Ethyl Corp. Schnectady Chemicals, Inc. 

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