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Acifluorfen-Sodium

2-nitrobenzoate, Sodium-5[2 chloro-4-(trifluoromethyl) phenoxy] 2 nitrobenzoate [Pg.131]

Uses Selective contact herbicide, absorbed by the foliage and roots with negligible translocation. Sunlight enhances [Pg.131]

This herbicide can be manufactured from m-cresol though one or two manufacturers use alternate route without use of m-cresol. BASF, Rohm and Hass and Rhone-Poulenc (now Mobile Chemical Co.) are manufacturing acifluorfen. Global demand is estimated to the tune of 750 tpa. [Pg.132]


R=Na, Acifluorfen-sodium R=CH3,Acifluorfen-methyl R=C2H5, Acifluorfen-ethyl... [Pg.452]

Diphenyl ether herbicides. The diphenyl ether class of herbicides belongs to a broader area of herbicides known as protoporphyrinogen oxidase (Protox) herbicides [20,21], Diphenyl ether herbicides were initially introduced over four decades ago in the 1960s with the discovery of nitrofen by Rohm and Haas (now Dow AgroSciences) [22] and bifenox by Mobil [23], These early diphenyl ether herbicides did not attain a significant role in the control of weeds in commercial crops until the 1970s, with the introduction of the trifluoromethyl compounds oxyfluorfen [24] and acifluorfen-sodium [25], Replacement of the chlorine with a trifluoromethyl group resulted in a dramatic increase in the herbicidal properties of these compounds, in terms of both potency and the spectrum of weeds controlled. [Pg.126]

Acetochlor amide Acifluorfen-sodium phenyl ether Aclonifen phenyl ether Acrinathrin pyrethroid Alachlor amide Alanycarb oxime amide Aldicarb oxime amide Aldoxycarb oxime amide Aldrin halogenated hydrocarbon Allethrin pyrethroid Allidochlor amide Alloxydim oxime... [Pg.1005]

Tachigaren hymexazol Tackle acifluorfen-sodium Tairel benalaxyl Takeoff imazosulfuron Taktic amitraz Talcord permethrin Talon brodifacoum Talstar bifenthrin Tamaron methamidophos Tamex butralin Tandem tridiphane Tandex karbutilate Taredan cadusafos Targa quizalofop-ethyl Task dichlorvos Techlead ipconazole Tecto thiabendazole Tedion tetradifon... [Pg.1022]

Acifluorfen sodium Acifluorfen sodium salt Blazer Blazer 2L Blazer 2S Carbofluotfen Caswell No. 755D EINECS 263-560-7 EPA Pesticide Chemical Code 114402 HSDB 6551 LS 80.1213 MC 10978 RH 6201 RH 6205 Scifluorfen Sodium Acifluorfen Sodium salt of acifluorfen Tackle Tackle 2AS. Used for postemergence control of broad-leaved weeds and suppression of some annual grasses in soybeans. Registered by EPA as a herbicide. Solid, soluble in H2O (25 g/100 ml at 25 ) LCso (rainbow trout 96 hr.) = 31 mg/l, (bluegill sunfish 96 hr.) = 54 mg/l non-toxic to bees. Aventis Crop Science BASF Corp. Bayer AG Monsanto Co. [Pg.555]

Synonyms Acifluorfen-sodium Sodium 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-... [Pg.81]

Acifluorfen-sodium. SeeAcifluorfen Acilol 16 Cetyl Alcohol. See Cetyl alcohol Acimetion. See DL-Methionine Acintol 208. See Isooctyl tallate Acintol 736, Acintol 746, Acintol 2122, Acintol 7002, Acintol D60LR. See Tall oil acid... [Pg.82]

Rohm and Haas introduced recently two new members of the diphenyl ether group, namely 5-(2-chloro-4-trifluoromethyl)phenoxy-2-nitrobenzoic acid (acifluorfen, 4) and 2-chloro-4-(trifluoromethyl)phenyl 3-ethoxy-4-nitrophenyl ether (oxyfluorfen, 5) (Biroli et al., 1980 Theissen, 1982 Swithenbank, 1982). Acifluorfen is used as its sodium salt soluble in water. [Pg.582]

Acid yellow 73 sodium salt (INCI). See D C Yellow No. 8 Fluorescein sodium Acid yellow 23 trisodium salt. See FD C Yellow No. 5 Tartrazine Acifluorfen CAS 62476-59-9... [Pg.81]


See other pages where Acifluorfen-Sodium is mentioned: [Pg.44]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.1014]    [Pg.130]    [Pg.170]    [Pg.18]    [Pg.131]    [Pg.414]    [Pg.761]    [Pg.761]    [Pg.156]    [Pg.156]    [Pg.985]    [Pg.44]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.1014]    [Pg.130]    [Pg.170]    [Pg.18]    [Pg.131]    [Pg.414]    [Pg.761]    [Pg.761]    [Pg.156]    [Pg.156]    [Pg.985]    [Pg.463]    [Pg.555]    [Pg.715]    [Pg.748]    [Pg.1087]    [Pg.543]   


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