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है”ह”ह
IS 885 (1994): Common Names for Pesticides and otherAgrochemicals (Excluding Fertilizers) [FAD 1: Pesticidesand Pesticides Residue Analysis]
Indian Standard
COMMON NAMESFORPESTICIDESAND OTHERAGROCHEMTCALS (EXCLUDINGFERTILIZERS)
( Second Revision )
UDC 632.951 COM
Q BIS 1994
B U R E A U O F I N D I A N S T A N D A R D SMANAK BHAVAN, 9 BAHADUR SHAH ZAFAR MARG
NEW DELHI 110002
July 1994 Price Group 15
2009
Pesticides Sectional Committee, FAD 1
FOREWORD
This Indian Standard was adopted by the Bureau of Indian Standards, after the draft finalized by thePesticides Sectional Committee had been approved by the Food and Agriculture Division Council.
This standard lists the common names of certain pesticides and other agrochemicals used in agriculture,animal husbandry and public health.
This Indian Standard was first issued in 1956. The first revision was brought out in 1967. This secondrevision is being brought out incorporating common names of several chemicals being used in the countryand also to bring the standard in line with the international work being done in this field. In thisrevision, effort has been made to prepare a list of chemicals that do not require common names.
The common names used in this standard are the chemical names, in conformity with the English rulesof the International Union of Pure and Applied Chemistry ( IUPAC ) and the International Organiza-tion for Standard ( IS0 ), wherever, common names approved by IUPAC and IS0 do not exist, namesas listed in the Chemical Abstracts has been included in this standard.
In the preparation of this standard, reference has been made to the following publications:
IS0 257 : 1976 ‘Pest control chemicals and plant growth regulators - Principles for the selectionof common names’.
IS0 765 : 1976 ‘Pesticides considered not to require common names’.
IS0 1750 : 1981 cPesticides and other agro chemicals - Common names’.
The Pesticide Manual, Seventh Edition, 1983. The British Crop Protection Council, Croydon CR02TD.
IS 885 : 1994
Indian Standard
COMMONNAMESFOR PESTICIDESANDOTHERAGROCHEMICALS [EXCLUDINGFERTILIZERS]
( Second Revision )
1 SCOPE1.1 This standard comprises of an alphabetical list ofcommon names for pesticides and other agrochemicals(excluding fertilizers), together with their correspond:ing chemical names, structural and molecular formulaeand use.1.2 This standard also contains a list of chemicalswhich have been considered not to require commonnatnes.
2 OBJECTIVE . I
Acommon name is to provide a short, easily pronoun-ciable name for a compound, whose full chemical nameis too long and complicated, for use in commerce,industry, official regulations and specifications.
3 PRINCIPLES FOR SELECTION OFCOMMON NAMES
3.1 The common names shall be written or printed inlower case letters, for example, malathion.3.2 In the exceptional cases where the names areformed from the initials, they shall be written in capitalswithout intervening full stop, for example, BHC.3.3 When numerals and letters both occur in a commonname, the numerals shall be started from one anotherby commas and from letters (capitals only) by a hyphen,for example, 2,4-D.3.4 The common name shall normally apply to the purechemical of known structure, but in exceptional casesit may be given to a mixture of isomers, in which not
all. the isomers may have established biologicalactivities, for example, BHC.3.5 Consideration may be given to the coining ofcommon names for reaction products having anincompletely defined chemical composition but not fordeliberate mixture of active ingredients.3.6 A proprietary name shall not be considered as acommc& name unless the manufacturer has formallyagreed to:
a) not to use it as a.trade-mark; andb) to permit its use as a common name by giving
up rights to it by any other means conformingto the statutory provisions.
4 USE
The use of each compound is given according to thefollowing classification:
Acaricide = A Molluscicide = MBactericide = B Nematicide = NF u n g i c i d e = F Plant growth regulalors = PHerb ic ide = H Rodenticide =RInsecticide = I Avicide ’ =\’
5 COMMON NAMES
5.1 The common names of different pesticides andother agrochemicals (excluding fertilizers) have beenlisted in Table 1 in an alphabetical order.
5.2 The chemicals considered not to requiie commonnames have been listed at Annex A.
Table 1 Common Names for Pest Control Chemicals
( Clause 5.1)
Sl No. Common Name
(1) (2)
1. acephate phoramidothioate
2. acrylonitrile
3. alachlor
4. aldicarb
5. aldrin
6. allethrin
Use
(3)
Chemical Name Chemical Structure Molecular Formula
(4)
0, S-dimethyl acetylphos =
0@ (6)
CH3 S
>L - N H
‘CH3_0y---COCtr~ C4HI,,NOjPS
acrylonitrileC”z = C”.-_CN ’
C,H3N
, CzHs
2-chloro-2’, 6’-diethylN- methoxymethylacetanilide
C14 %o GINO,
2-methyl-2-(methylthio) =
propionaldehyde
FH3
carbnmoyloximeO-methyl CH3:S -_c
I- CH = N - O- CO -NH - CH3 C7H14N202S
I a
CH3
Product containing 95% of HHDN(see Sl No. 194)
.
(MS)-3-allyl-2-methyl-4-oxocyclopent- 2enyl (lRS)- ck-trans-chrysanthemate
C1 2H9C16
CH 3 CH 3
C = C H CH2CH = C H ,
CH 3CH 3 0
c19H2603
,alphamethrin
8. ametryne
9. amidithion
I (S)-a&a-cyano-3-phenoxybenzyl
(1 R, 3R)-3(2,2_dichlorovinyl)-2
2-dimethylcyclopropanecarboxyIateand
(R)-alpha-cyano-3-phenoxybenzyl
(1 S, 3S)-3-(2,2-dichlorovinyl)-2,
2dimenthylcyclopropanecarboxvlatcin the ratio 1 : 1
H N-ethyl-N’-isopropyl-6 methylthio-I,
CH3S u”;& NHCH,CH,
C9HuN5S3,5-triazine -2,4-diyldiamine
YNHCH(CH,),
A S-2-methoxyethylcarbamoyl = C,H,,NO&
I methyl 0, Odimenthyl phospho =dithioate
(CH30)2;-S-CHZ-CO - N H -CH2-CH2-0CH3
si
- 11. amitm[e
12. anilofos
&
13. antu
14. asularn
15. altwine
H 3-ii t71ir10-1}/-1, 2, 4-traizole
Table 1 ( Corrt@w/ ).=
S1No. Common Name Use Chemical Name*
Chemical Structure Molecular Forsnuln z
(1) (2) (3) (4)..
(9 ““ (6)mm,x
CH3 CH310. amitraz A N-methylbis (2, +xylyliminu =
o
I
o
C19H23N3
CH3 - / \ N= CH—N—CH=N / \ ~H3I methyl] wninc — —
CH3.!/
/N\
f 1(
N
N.
NH 2Ii S-44kwo-N-isopropyl =
~..
carbaniloyhnclhyl O. O-dimetlwl
-o-
CI /_\ ~COoCli#(OCH3) ~[Jhosp}~]rt}n~dltl]lotitc
CH(CH ~2
.!!IHC.S6NH2
@
)“ \I\/
11 methyl sulphimil ylcarbamate
G
Hz~ / \ ~02_ ~H_~Q —OCH3CJ+10N204S
—
R 1-(1-naphthyI)-2-thiourea
H 24c~m-4*ttiyloarltiti-tipmpylamin0-1,3, S-triazine
(CI+3 )2CH – NH \ c1
YN)’N ‘/N
‘Y’NH — C2H5
C,3H1QCIN03PS3
.. Iii. azvnethiphos 1 .$6-chloro-2, 3dih@o-2*xn-
OXWOIO-[4, 5-4 pyridin-11-ylmethyl0,0-ctirnell@ phosphnmlhiwte]
17. azinphos A
ethyl 1
18. azinptws A
methyl J
m
19. bartxm H
20. benalaxyl I?
21. bendkwarb
.
I
S-[.3, J-di hydm-&oxcJwmo-
[d] [1, 2,3] triazin-3-@wthyl) 0,0-diethyl phosphorodithmate
S(3. [email protected] [d] [1,2,3]
mi;win-3-vIrnethyl) “O, CWmethylphosphorodiothioale
d-chlombut-2-ynyl 3-chlorocarbani-Ialc
rncthyl N-phcnylacetyl-N-Z 6-xylyl-DL- idanillate
2,2-dimeihyl-1, 3Aenwdioxol-4-yl =rncthylcarbatrliite
iXi2!W(OCH3)2
C..HIOCIN:O+’S
Q./~NH —CO—0CI+2C==C CI+2CIc~#Igclyl:
—-
CI cti3;
0/ J ~~2~~\ , &j_~”3‘\—.-.. N
o
CH3 /’ CH ~
J
Q)(:} “ c“’. 0 CH3& . ...C’j--.-...NH —ct+~
-d
Tabk 1 (Continued)t;
Chemical Structure Molecuk- Formula E. .S1 No. Common Name Use Chemical Name-,
(1) (4 (3) (2%;
22. henodanil I: Z-iodobenzanilide
23. benomyl F methyl l-(butylcarbamoyl)zimidazol- 2-ylcarbamate
24. bensulide
2.5. bentazone
26. benzoylpropethyl
ben-
H S-2-benzenesulphonamidoethyl 0, O-di-isoprophyl phosphrodithioate
H 3-isopropyl-Q-H)-benzo-7 1 ,thiadiazin-&one 2.2-dioxide
H ethyl-N-benzoyl-IV (3,dichlorophenyl)- DL-alaninate
(5)
Q- CO____N” q-JIco- NH(CH&CH,
NH - CO - OCHs
(61
%HldNO
C14W’J403
o-/ \ SO,-NH--
C,,H,,NO,PS, ^
3-
4- o- Cl-i3
./’ co LHCO-oCH, CH 3- IN/
o-
3 ClI
27. bcnzethiazumn
29 13HC
29. binapacryl
3(?. bitertanol
-4
31. IWMC
H LbenzothiazoI-2yI-3 -mctiyluma
“I
AF
F
1
1, 2, 3, 4, 5, 6-hexachlorocydo =hcxane (Mixed isomcra)
2-sec-butyl-4, 6-dinitrophenyl 3-methylbut-2-enoate
aU-mc-l+iphenyj 4yk@-3,dimethyl-l<w-1,2, 4..tnazol.l-y?jbutane-2@l [ratio of raceinatea (M/S,2Rs) and (MS. Xl?) is about 20: 80]
2-sec-butylphenyl methykwbarnate
s
(“JY NH— CO— NHCH3
:1 IN
c1(.2oicl cl
cl
,NQ2.
02N -Q-K. \ 0-CO-CH=C(CH3)2,
\cHc2H 5
tH3
m “H/ \ i \ o-7H4H-c(cH3)3
N\
IjJ
CH3NHC0-~ - fN3
0;,.,&H-CH2-CH3
J
..
Table 1 ( Continued) z
!<I No. Common Name Use Chemical Name Chemical Structure Molecular Formula B. .
32. brodifacoum
33. bromacil
34. bromadiolone
35. bromophos
R 3-[3-(l’-bromobiphenyL4-yl)-1, 2, 3,Metrtmhgdro-1-naphthyl]-4-hydroxycoumarin
H 5bromo-3-set-butyl-6-methyluracil
R 3-[3-(4’-bromobiphenyM-yI)-3-hydwxy-l-phenylpropyll- 4hydroxycoumarin
1 0-4-bromo-2,5dichlorophenyl 0, O- _dimethyl phosphorothioate
36. hromophos-ethyl
37. bromopropylate
38. bromoxynil
3 Y . brompyrazon
G
‘lo. bufenwrb
I 0-4-bromo-2, 5-dicholorophenyl 0 ,0-diethyl phosphorothioate
A isopropyl 1, -I‘-dibromobenzilate
Br
Cl,
.OH
CN
3,5-dibromo-+hvdroxvbenzonitrilc_
Br Br
OH
5-amino-4-bromo-2-phenylpyridazin-3(2H)-one
C$IiBr2N0
An isomeric rextion mixture contain-ing approximately 3 parts by mass 01.(i) j-(1-methylbutyl) phenyl meth+carbamate and 1 part by mass of (ii)3-(1-ethyl=propyl) phenyl methylwr-bama te
42. butachlor
43. buturon
Table 1 ( Continrred > E
Sl No.3E
Common Name IJse Chemical Name Chemical Structure Molecular Formula 01. .
(1) (2) (3) (4):. (6) 5
41. buprofczin I 2-tert-butylimino-3-isopropyl-5-phe Ct,H2,N,0SP
nyl-1,3,5thiadiazinan&one
H N-butoxymethyl-2-chloro-2’, C,,H,~CINO~6’-diethyl=acetanilide
I-1 3-(4-chlorophenyl)-l-methyl-l-( l-m C,,II,,CINIOethyl = prop-2-ynyl) urea C H , .
N H - C O - N d - H C = C H
44. butylate
45. captafol
46. captan
Ci ,H23NOSH S-ethyl di-isobutyl (thiocarbanl.ltc [(CH,)2CHCH2]2-NCO- S-CH2-CH,
0
F N-(1, 1, 2, 2-tetrachloroetylthioj C,,H,CI,NO,Scyclohex-4-ene-1,2- dicarboximide 2 -CHCI 2
0F 1V-(trichloromethylthio) cyclohex-4- 0 C,II,CI,NOZS
ene-1,2-dicarboximide
48. carbendazim F
49. carbofuran 1
50. carbophe = nothion A S-J-chlorophcnylthiomethyl 0 , O-I dicthyl phosphorodithioate
51. carboxin I 5,6-dihydro-Z-methyl-l, 4-oxathi-inv-Scarboxanilide
52. cartap I S, S’-2-dimethylaminotrimethylcnchis (thiocarbamate)
53. chinomelhi = onate AF
54. chloramben II
methyl benzimidazol-7-yI~mdmate
2, 3-di hvdro-2, 2-dimethylhen-zofuran-7-91 methylcarbamate
6-methyl-l, Sdithiolo[4, 5-b] =quinoxalin-2-one
S-amino-Z, 5-dichlorobenzolc acid
O C O - N H C H ,
2N H - C O - O C H ,
OCO-NHC.Y3
3_- /
SCH ,SP(OC,H& 2
(CH3),NCH(CH&ONHd2
CO-OH/cc3 Cl
Cl NH2
Table 1 ( Con~inrred ) z
Sl No. Common Name USC Chemical Name Chemical Structure Molecular Formula %
(1) (2) (3) (4
(6)55. chlorbenside A +chlorobenzyl 4chloropkenyl sul- C,,N,,~C’I,S
phide
56. chlorMam (BIPC)
57. chlordanc
chlorfenac
59. chlorfenson
II l-methylprop-2-ynyi 3-chlorocarhani-late
I 1,2,&j, 6,7,8, S-octachloro-2,3,3a,5, 7. ?a-hesahydro-4, 7-methanoin-dcne
1-I (2, 3,6-trichlorophenyl) acetic acid
A l-chlorophenyl_I-chlc~robenzcne =suI-phonate
C,“H,CI,
60. chlorfensul = phideCl
u-/ \
A l-chlorophnzyl 2,-I, Qrichloro = bcn-Cl C,,lI,CI,NIS
zenediazosulphidc-
Cl
.
61. Chlorfelwinphm I 2-chloro-l-(2, 4-dichlorophenyl) vinyldiethyl phosphitfe
62. chlorrnequat @ should be P 2-chloroethyltri methyl = ammoniumstated which anion is present, ionfor example, chlornwquat chloride)
,
63. chlorobenzilate A ethyl 4, 4’dichlorobenzilate
6<. chloronebE
F l,4dIcbloro-2, 5-dkrjeChoxybenzene
65. chloroph;l = cinone R 2-[2?4-chlorophenyl)-2-phenyl=acetyll Mm-1, %lione
CHCI
ClC/+ CH2N+(CH3)3
CO”OCH2-CH3
CKYe”AH
C5H,3CIN
66. chloropicrin i trichlorwritrornethane ~!\—C-N02~,/-
Table 1( Continued ) E
Chemical Structure Molecular Formula ESt No. Common Name Use Chemical Name
(1) (2) (3) 8 (6)
CgCl,N~67. chlorothaldnil F tetrachloruisophthalonitrile
68. chloroxuron
69. chlorpropham
70. chlorpyrifos
H 3-[4-(4-chlorophenoxy) phenyll-1, l-dimethylurea
H isopropyl 3-chlorophenylcarbamate
I 0, O-diethyl O-3, 5,6-trichloro-2-pyridyl phosphorothioate
71. Chlorpyrifos methyl I 9, 0-dimethyl O-3, 5, 6-trichloro-2-pyridyl phosphorothioate
CN
cl+ 0 a N”-CO-N&H, )* ClsHlsClN202
S
Cl 0;(OCH2CH &
Cl. Cl
S
Cl 08(0CH&
Cl Cl
.,.
!-4
z*fq,E
C3“
t+Az
.,
......—
C4
15
Table 1 ( Continued) t;’00
Chemical Structure Molecular Formula %SI No. Common Name Use Chemical Name
(1) (2) (3) (4)
. .(5) (6) Gx
78. coumaphos I O-3-chloro-4-methyl-2-oxo-2H-chro m e n 7-yl 0, 0-diethy) p h o rphorothioate
79. coumatetralyl
80. cyanazine
81. cycloate
82. Cycl uron
R 4-hydroxy-3-(1, 2, 3, 4-tetrahydro-1-.naphthyl) coumarin
H 2-(4-chlorod-ethylamino-1, 3, 5-&i-azin-2-ylamino)-2-methylpropionitrile
H S-ethyl N-cyclohexyl-N-ethyl(thiocar-bamate)
H 3-cyclooctyl-1, I-dimethylurea
CH3.~
tiH-CHp-CH3
NCO-SCH2 -CH,
LH2 CH,
NH-CO-N(CH3j2
C19H1403
C,,H,$OS
C~lH$20
83. cyfluthrin I
84. Cyhalorhrin
5 85. cyhexa ti n
86. cymoxanil
87. cypermethrin
I
A
F
I
cyano-(4-fluoro-3-phenoxyphenyl)- _I 1methyl-3- ( 2 , 2-dichloroethyl)-2, 2-dimethyl-cyclopropane carboxylate
:;; D&&i lf c”z:rO
C H , C H ,
(RS)-a&a-cyano-3-phenoxybenzyl(2) CF,-(IRS, 3RT)i2-Chloro-3i_~~~t~~:. \ , Hfluoropropenyl)-2,cyclopropane = carboxylate c,/c=ctl
CNI
(‘23H,gClF3N03
tticyclohexyltin hydroxide
1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea
6H
CN
CH 3-CH2 - N H - C O - N H - C O - & N O C H 3
C19H3d)Sn
C7H,o%%
(RS’)-a&z-cyano-3-phenoxybenzyl( lRS)-cb-truns-3-(2,2- dichlotovinyl)-2,2-dimethylcycloptopanecatboxylatc
Table 1 ( Continrted) tf
Chemical Name Cheinical Structure Molecular Formula ESI No. Common Name Use . .(6) 5;x
%H6C1203
( 4 ) (5)(1) (2) (3)
88. 2,4-D H
89. dalapon H
Cl
Cl--c-s-/ \ OCH2-COOH- -
(2,4-dichlocophenoxy) acetic acid
C3H4a2022,2-dichloropropionic acid
O(CH &-COOH
F’CH3-y-COo#:
ClWGV’3N-dimethylaminosuccinamic acid90. daminozide H
(CH,),NNHCO-CH2CH&OOHt e t r ahyd ro -3 , Sdimethyl-1, 3, 5-thiadiazine-Zthione
WloW2F91. dazomet
c10bOa203
C3H5Br2CI
H
N
4-(2,4-dichlorophenoxy) butyric acid
1,2-dibromo-3chloropropane
92. 2,4-DB
‘93. DBCPBr-CH2-CHBr-CH2CI
Reaction mixture of 1, 2-dichloropropane (see Sl No. 109) and1, 3-dichloropropene (see SI No. 110)
CICH &HCH 3+ Cl
“CH2 \c=c F “‘CH2 \c=c /
H ’ \C,H ’ ‘H
(9
94. D-D mixture ‘N
95. DDD
96. DDT
97. delthamethrin
z 98. demeton-0
99. demeton-O-methyl
100. demeton-S
101. demeton-S-methyl
AI
AI
AI
AI
1, 1-dichloro-2, 2-bis (4-chlorohenyl)ethane
CHCI,
1, 1, 1-trichloro-2, 2-bis ’(4-chIorophenyl)-ethane CI qH +u
CCI,
(S) - alpha-cyano-3-phenoxybenzyl(lR)-ck-3-(2,2-dibromovinyl)-2,dimethyl =cyclopropanecarboxylate 2- iir
O,O-diethyl o-2-ethylthioethyl phos =phorothioate (C,H, O),P-0-CH 2-Cb++-CH2-CH3
0-2-ethylthioethyl 0 , 0-dimethylphos = phorothioate
S
(w,O)2 !-O-CH2 -CH,-S-CH&CH,’
6it
0, 0-diethyl S-2-ethylthioethyl phos =phorothioate
(C2H50)+-S-CH2-CH2-S-CH2-CH3
S-Zethylthioethyl 0, 0-dimethyl phos= phorothioate (CH3 O& P-S-CH, -CH2-S-CH2-CH3
C,H ,903PSi
(%H1903PS2
(1) .,-’
102. desmctryw
103. diazinon
Na 104. dibrommchlompmpnc
10.5. dicarnba
(3)
H
AI
N
H
106. dichtobetil H
107. dichlone,, F
(4)
2-isf~prOpYhtmino-4-mcthylamino.~-n_t{!th-ylthif)-1, ~, .fLtdazine
O, 0-diethyl O-2-isopropyl-&methyl= pyrimidin-4-yl phnsphomthioate
1, 2-dit)~]mf}-3-ehlorf>ptipane
3, 6-dichlom-o-atisic acid
2, 6dichlombnmnitilc
~, 3dichlom-1, 4-naphthoqtinonc
(5)
cH3’y>yNHcH(cH’)’
YNHCH3
CH3 M
Y’
Y CH(CH3)2‘1\N
0:(OC2HJ2
s
8rCH2CHBt-CH2CI
COOH
cl‘(!X/ 0CH3
I\ ‘,
‘N
C&15N5S
.
C12H21N20#S
● “
108.
1(!9.
110.
dichkwophen Ii
B
I. ?-dichlo =mprqxdnc I
1, %-dio!)lu = rup:upcnci
i111. dichlorvos
.;:, l,$it:$,,!.
[:
H
4, 4’-dichlmn-2, 2’methyltxtediphcnol
OHI
Icl
2, 2-dichlorovinyl dimethyl ph~s~hiit~
i
!.CH30)2p-ocH=cci 2
cl o
>PI.....—
5-dimethyl/\No
-
)
.—. CH 3
c1 o’ CH s
\-I.,.
‘1’al)lt! I ( <:0)11;////(?(/ ,-- .-. ..——. .—.. %. . . .. .. —.. ——..— ,-; t,.], nwrl Nit IIW IJsc C!wtnimrl PfiIIUC
—.(’hcwttu, ‘,tlllcitfik KIoIw-uIw Formuln :
il,i (2) (3) (4). .
i<: (6) l.-
yl-i 2 z. &
i 16. dirxr]tcrpbos
i .,1:
117. dit:ldrin
118. dimrochlor
119. dicthyl = Ioluarnidc
A 2,2. 2-trichloro-1, l-bis(cIchlmophcnyl) ethanol
1 (~-z-dif.nt~thylalrba rr.wyl)-l.-mdhylvinyl dirwthyl phwphak
A perchloro-1, 1‘bicyclopcnta-2,4-dicnyl
I N, N-diethyl-m-toluarnidc
,H
[ produci contitining 85 percent ofHEOI) (see fafer-)
“-?
(CH30)2P~,
C=c
(’tHJ6NO#
Ci2H8C160(IiEOD)
CO- N(C2ii5) 2I
C, ZH,7N0
d/\ CH3
3
0
LL
.-4
*.lahle 1 ( C’o,Uil?lrtri ) ..- _.
- -SI IVI,. t‘ommon Name 1 ke t’hemical Nanir Chemical Structure ~,i~tl,.cl_‘;ri-~,i-. ,,I. ::
, c4
; ‘!t\ dlmidaznn
b 2-see-butyl-4,6_dinitrophenylisopropyl carbnnate
(CH ,)2CHO-CO-0I
FH 3
A An isomeric reaction mixture ot (1) 2.F 6-dinitro-4-octylphenyl crolonztcsand
(if) 2. 4-dinitro-6-c,ccylphenylcrotonate\ NOTE - I he mixture nor-maliv contains bchvecri 4 and 5 partsofisbmen ol2.4-dlnitro-6octylphenyl
O-CO-CH=CHCH,
crotonates to Z 1l.1~ vf the 15omt’rs ol2, 6-dinitro-l-oc:t\rll~tl~,~\,~ crotrinntv\ 0 2N
I CH,(CH2‘),,CH(CHzjs_nCCi3
CHdCH,),,CH(CH&,CH~ [n=O,l,Z]
[“T”i’l04
a
3;
‘i:.-
1 2 9 . dinosauj
130. dinoseb
H 2-(1-methyIbutyl)-4,6dinitrophenolI O.,N
H 2-see-butyl_4,6dinitrophenol
132. dioxathion
133. diphacinone
’ CHCH2CH2CH,0 I
CH3 CHS
C&u’W~
CH3CO-0 cH3
O2NC,,NdW,
sNO2
C,&,0&S4
Sb(OCHzCHa),
S;@CtizcH~ )2
S
c,,Pl@,
NO2131. dinoseb acetate H 2-see-butyl-4,6dinitrophenyl acetalc
I S, S’-(l, 4dioxane-2,3diyl) 0, 0, O’,O’-tetraethyl bis(phosphorodithioate)
R 2-(diphenyIacetyI) indan-1,3-dione
Table 1 ( Continued ) i3
Chemical Structure Molecular Formula %(II. .SI No. Common Name Use Chemical Name
(1) (2) (3) (41 (6) 5z
Cl6Hl7NO134. diphenamid
135. dipropetryn
136. diquat (it should be stated
Ewhich anion is present,for instance diquat dibromideor diquat dichloride)
1 3 7 . disul
138. disulfoton
H N, N-dimethyldiphenylactamide
H 2-ethylthio-4,6-bis (isopropylamino)-1,3,5triazine
H 9 , lo-dihydro-Sa, lOadiazoniaphen-anthrene ion
H 2-(2,4dichlorophenoxy)ethyl hydrogen sulphate
1 0, 0-diethyl S-2-ethylthioethyl phos- sphorodithioate (C2H50),PSCH2CH2SCH2CH3
‘b’d2
%H:,N~S
C&$@@’
0CH2CH20S0,0H
QI\ / (4QI
\ /
-n
Jib
Table 1 ( Contimed) ’ ‘5
SI No. Common Name Use Chemical Name Molehuhr Formula EChemical Structure
(1) (2) (3) (4
145. endosulfao A 6,7,8, 9, lo-hexachloro-1,5,3a, 6,9,I 9a-hexahydro-6, 9- methano-2, 4, 3-
benzodi-oxathiepin 3-oxide
147. endrin I 1, 2, 3, 4, 10, lo-hexachloro-6, 7-V epoxy-l, 4,4a, 5,6,7,8,8a-octahydro-
endo-1,4-exe-5,S-dimethanonaphthalene
148. EPN
146. endothalsodium H disodium 7-oxabicyclo [2. 2. l] hep-t ane -2 ,3 -d i ca rboxy la t e
I O-ethyl 0-4-nitrophenyl phenylphos = .phonothioate
149. EPTC
150. erbon
H S-ethyl dipropyl (thiocarbamate)
I 5)
Cl
c’ Cl OJ@I Cl$20
Cl
ClCOONa
COONa
_~~[CHS(CH2),],NCO-SW2 CHs C,I-I,,NOS
H 242, 4, 5trichlorophenoxy) ethyl-2,2dichIoropropionate
0-CH2 -CH2-0-CO-Ccl2 -CH, C,,H9C&
1.51. e~halfluralin
152. ethepon H 2chloroethylphosphonic acid
153. ethion
154. ethoprophos
155. etrimfos
156. fenamiphos
H N-ethyl-N-(methylallvl)-2, 6-dinitro-4-trifluoromethylaniline
A 0, 0, 0; O’-tetraethyl S, S’-I methylene-bis (phosphorodithioate)
N O-ethyl S, S-dipropylphosphorodithioate
CFsF
HI
CH2 -C=CH2
CH2 CH,
0
CICHICHzk0H)2
8[C, Hs 0) ,PS
2
$2 HI 0) 2Ps
!
I 0-6-ethoxy-2-ethylpyrimidin-4-yl 0,0-dimethyl phosphorothioate
C,d-I,7W,PS
N ethvl, 3-methyl+(methylthio)-phenylisopropyl = phosphoramidate OiNHUi(CH;) C,,H,W,E
I2
0CH2 CH. E
Table 1 ( Continued ) G
SI No. Common Name Use Chemical Name Chemical Structure ZEMolecular Formula +.JI. .
(1) (2) (3) (4) (6) &E
157. fenarimol F (*)-2, 4’-dichloro-alpha-(pyrimidin- C,~H,ZCI~N,O5-y]) benzhydryl alcohol
158. fenazaflor
4:159. fenchlorphos
160. fenfuram
161. fenitrothion
162. fenoprop
I 0, 0-dimethyl O-2,4,5-trichlorophenyl phosphorothioate
Pphenyl5,6-dichloro-2-trifluoromethylbenzimidazole-l-carboxylate
0
F 2-methyl-3-furanilide
(YI I
Cl
Co-NH
I 0, Odimethyl O-4-nitro-m-tolyl phos-phorothioate
H (T)-2-(2, 4, S-trichlorophenoxy)propionic acid
C9H7Cl303
O /“\I
[’o
Z
N-n
..-—
s-=.
Table 1 ( Continued )
SI No; Common Name Use Chemical Name
(1) (2) (3) (4)
169. fenuron H l, l-dimethyl-3-phenylurea
170. fenvalerate
s171. ferbam
172. fluazifop
173. fluchloralin
I (RS )-alpkr-cyano-3-phenoxybenxyi-(RS )-2-(4-chlorophenyl)-3-methyl-butyrate
F iron tris (dimethyldithiocarbamate)
H (RS)-2-[4-(5trifluoromethyl-2pytidyloxy) phenoxy] propionic acid
H N-(2-chloroethyl)-aI@m, alphaalpha-trifluoro-2,6-dinitro-N- propyi-P-toluidine
(CH
Chemical Structure
(5)
NH.CO.N(CH&
Cl/0\ I
& CH.CH.CO.OdH
-+
[(cH~& NCSS-1 5’” 3
CF,o 0 0 O:;iO.OH
-
NO2
cF3
G-
/ \ N/CH2cH2C’
\ (CH 2)2W
NO2
Molecular Formula E
174. flucythrinate
175. fluometuron
176. fluvalinate
177. fonofos
178. formothion
179. fosetyl
(RS)-alpha-cyano-3-phenoxybenzyl(S)-2-(4-difluoromethoxyphenyl)- 3methybutyrate
1, 1-dimethyl-3-(alpha, alpha, alpha-trifluoro-m-tolyl) urea
NH.CO.N(CH 3 jz ‘GhVW
CF3
O-ethyl S-phenyl (RS)-ethyl phos-phonddithibate
S-(N-formyl-N-metS.ylcarbamoylmetfiyl)-0, O-dimethyl phosphorodithioate
ethyl hydrogen phosphonate
0il
CH2CH30ToHH
~1&50ps2
C&NW’S,
c2H@3p
Sl No. Common Name
(1) (2)
180. Furathiocarb
181. furrnecyclox
!li182. gamma-HCH or gamn~a-BHC
183. gibberellic acid
184. glufosinate
Use
(3)
1
F
I
P
H
Chemical Name_
(4)
butvl 2,3-dihydro-2, 2-dimclhylbcn-zofkran-7-yl N , N-dimethyl-N. N-dithiocarbamate
methyl N-cyclohexyl-2, 5-dimcrhyl-furan-3-carbohydroxamate
(1, 2, 4,5/3,6)-l, 2, 3, 4, 5,6-hexa =chlorocyclohexane
(3S, 3aS, 4S,4aS,7S,9aR, 9bR, lZS)-7,12-dihydtoxy-3-methyl&methylene-2_oxoperhydnMa,7-methano-9b, 3-pmpeno- [ 1,3-bifuran-4] carboxylic acid
-.
LX-homoalanin-Cyl (methyl) phos-phinic acid
Chemical Structure Molecular Formula F
CH3 CH3I I
?.CO.N-S-NCO.O(CH 2)3CH3
CH3ox<I0
\ ’CH3
Cl Cl
/OH
pJ-g
CH2
.OCH !CH CH CHCO Ot’3, 2 2, . : W 12NW’
6H i4H2
185. glyodin F
186. glyphosate H
187. glyphosine P
18ti. gwtzatine F
-.wU
189. HCH or BHC I
190. H~OD I
2-heptadecyl -2-imidazoiine acetate
N-(phosphonomethyl)glycine
N, i?-bis (phosphosmethyl) gl ycine
1,1 ‘-iminodi (octamethylene)diguanidine
Mixed isomers of 1,2,3,4,5, 6-hexa-chlomcydohexane
(IR,4S, 40LY,3R,6R, 7S, &S,8uR)-1, 2,3,4, 10, Whexachloro-1, 4, 4a, 5.6,7,8, 8a-odahy&o-6, 7-epoxy-1.4, 5,8- dirnetharmraphlhakme
NH
(’Y
C&(cH 2),5 -CH3,CH3-COOH
IN
o
H0.COCH2NHCH2!(OH)2
oHO. COCH2 N[cH$(oH)-2]
NH~HII
NH2 CNH(CH fla NH(CH2)aNHCNH z
cl
c1
:+.
c!
cl “ c1
cl
cl
&
clcl c1
“o cl
c1
cfjH&l~
c&cl&r
.
um
Table 1 ( Confinued )
S1 No. Common Name Use ~hcmkal Name Chemical Structure MolecularFormula
(1) (2) (3) (4) (5) (6)
191. h@ach]or
192. hCXWhlOrohenzene
193. hexrzinone
194. HHDN
195. IM
[ 1,4,5,6, 7,8, fi-heptachloro-la, 4.7,7a-!etrrrh@[u-4,7.. methfinoindene
F hexachlcumhenzene
M:yk)l]cxyl-rj.di methy+rminn-1-methyl-1, 3, 5-trinzine-2, 4 (Ilf, 3H)-dionc
I 1,2,3,4.10, 10-hexiictrlofo-1, 4, &$,8: fla-hexahydm-tio-l, 4-errdo.5, fJ-drmethano-naphtalenc .
P indol-3-ylac@ic acjd
cl c1c1
@
I ccl I
clc1c1
cl
@
c1/-’
I-’% ‘c,
cl
‘CH3)2NWNf4
‘l-fQ 0:
C12H20N402
C12H8C[6.
(l-J-/’ N.=\ I
CHCO.OH,
C’10H9NC)2
1 9 6 . I B A P 4-indol-3-ylbuttyric acid
197. IBP F S-benzyl 0, 0-diethylphosphorothioate
198. ioxynil
199. iprodione
rt;
200. isazofos
201. isobenzan
H 4-hydroxy-3, S-di-iodobenzonitrile
F 3-(3, Sdichiorophenyl)-Nisopropyl-2,4-dioxoimidaaolidine-l-carboxamide
N O-khloro-I-isopropyl-W-1, 2, 4-tri-azol-3-yl 0 , Odiethyl phos-phorothioate
I 1,3,4,.5,6,7,8, ILoctachioro-1,3,3a,4,7,7a-hexahydro-4,7methanoisobenzofuran
Cl / \ClD-
I
d\ / OH
CO.NHCH(CH&Y
C7H&NO
w3)2CH\N_ N. s
aANA &(OC2H5) 2
Cl ClCl‘SI C
Cl O'Cl
Cl Cl
(-%H9Ci20
.Table 1 ( Contimed) E
zChemical Structure Molecular Formula (n. .S1 No. Common Name IJse Chemical Name
(1) (2) (3) (4 (5) (6)L
3202. isofenphos I O-ethyl O-2-isopropoxycarh~l~~ l-
phenyl isopropyl phos-phoramidothioate
203. isonorunon
204.%
isoprocarb
2 0 5 . isaprothiolane
206. isoproturon
II A mixture of the two isomers: 1, I-dimethyl-3-(perhydro4,7- methano =inden-1-yl) urea and l, l-dimethyl-3-(perhydro-4,7- methano = inden-2-yl)urea
1 I-isopropylphenyl methylcarbamate
F di - i sopropy l 1 , 3dithiolan-2-ylidenemalonate
s CdbW,~
07CH*CH3NHCH(CH &
, NH-CO-N(CH &
?CO.NHCH 3/0 CWH,) *
\ I
Cdb,W
‘%H,W,
H 3-(4-isopropylphenyl)-1, ldimethyl NH.cO.N(cH,), C12HlSNZO
urea
,
207. kasugamyoin
I!%. kinoprcne
g209. lenacil
210. leptophos
211. lindane
212. linuron
F 1 L - 1,3,4&S, 6-l-deoxy--2,3,4,5, C14HAW96- penta =hydroxycyclohexyl-2-amino-2,3,4,6- tetra =d e o x y -4- ( a!pho - iminoglycirio) -U&I -D- arabino- hexopyranoside
I prop-2-ynyl (1) - (E, E) -3, 7, 11 - C, ,I 12&O,
trimethyldodeca- 2,4-dienoate(C”,),C”C”,C”,C” 2CHCT ”
H ’ c=c$=c<Io OC”. 2 -C C”
C”,
.- \I 3-cyclohexyl-l,S, 6,7-
H
A 0
Qrf
IY
N
0‘0
C, ,l-l,sN202
tetmhydroxyclo = pen tapyrimidine-2,4 (33 - dione
I O-4-bromo-2, S-dichlorophenyl O-methyl phenylphosphonothioate
I Product containing not less than 99percent of gamma - HCH or gamma -BHC (see SI no. 182).
H 3-(3,4-dichlorophenyl) -l-methoxy-l-methylurea
Cl
Table 1 ( Continued ) s%
St No. Common Name Use Chemical Name Chemical Structure Molecular Formula (h. .
(1) (2) (3) (9 (5) (6) Ex
7 CH2C0.COC2H5
213. malathinon t S-l, 2-bis (ethoxycarbonyl)ethyIO,O- (CH &CH ( %1~1904f%
dimethyl phosphorodithioate C0.0C2HS
214. maleic hydrazide
215. mancozeb
216. mancb
217. mazidox
H 1,2-dihydropyridazine-3,6dione
F manganese ethylenebis (dithiocar-bamate) (polymeric) complex \vithzinc salt [complex of zinc and manebcontaining 20 percent of manganeseand 2.5 percent of zinc. It should hestated which salt is present, for ex-ample, mancozeb chloride] (Chemicalstructure is fully not known)
F manganese ethylenebis (di thiocar-bamate) (polymeric) [chemical struc-ture of the product is not yet fullyknown]
I tetramethylazidophosphonic diamideW3W\ 4 0
(CHS)~N/ ‘, Ns
C4H4N,02
[C,HeMnN&]*(ZN)
C,H&OP
218. MCPA H 4-chloro-0-tolyloxyacetic acid
219. MCPEi
220. mecarbam
2 2 1 . mecoprop
222. MEMC
5
223. menazon
224. mephosfolan
H 4-(4-chloro-0-tolyloxy) butyric acid
A S-(N-ethoxycarbonyl-WmethylcarbI amoyl = methyl) 0, O-diethyl phos-
phorodithioate
H (*)-2-(4-chIoro-O-tolyluxy) propionicacid
F 2-methoxyethylmercury chloride
A S-4, 6-diamino-1, 3, 5triazin-2-ylI methyl 0, 0-dimethyl phosphor0
dithioate
==
, C,H&Q
C,,H13C’03
-CH3I
CzH50.CO.NCO.C” 2SP(OC2” 5)2
Cl\
’ # Cl&,lC~O3.
CH ,O-(CH 2) ,-HgCI C3H7ClHg0
S
H2Ny NY CH,S&OCH,),WWW2’%
I diethylj-methyl-l, 3-dithiolan-2-yli = C8H16N03PS2denephosphoramidate
Table 1 ( Continued )
SI No. Common Name USC
(1) (2) (3)
225. Metalaxyl F
2 2 6 . metaldehyde
227. metam sodium
5228. methabenzth= iazuron
229. methacrifos
M
I
Chemical Name
methyl N-(2-methoxyacetyl) -N-(2,6-xylyl) - LX-alaninate
r-2, c-4, c-6, c-8-tetramethyl -1, 3, 5,7-tetraoxocane
sodium methyldithiocarbamate
1-benzothiazol-2-yl-1,3-dimethylurea
O,O-dimethyl (E)-0-2-methoxycar-bonylprop-l-enyl phosphorothioate
0, S-dimethyl phosphoramidothin:rrt
Chemical Structure Molecular Formula E
CSH1604
CH3-N-Na=CS-SH C2H4NNaS2
(CH3wO;\C=C,cH3
d H/I I
‘CO.OCH,
CH30PSCH 3INH2
C7H13W’S
C2H9N0,PS
231. methidathion I
232. methomyl I
233. methoprene I
234. methoxychlor
.235. metiram
236. metobromuron H
S-2, 3-dihydro-5-methoxy-2oxo-1, 3,4-thiadiazol-3-ylmethl 0, 0-dimethylphosphorodithioate CH30XS~:H2S~(OC”,),N-
S-methyl N-(methylcarbamoyloxy) =thioacetamidate
CH3S\
/
C=N-OCO.NHCH3
CHs
isopropyl F-E) - W9 -ll-methox~-3~7,11-trimethyldodeca-2,4- dienoatq
1, 1, 1-trichloro-2, 2-bis (4-methoxy-phenyl) ethane
- c+=& f” 0 OCH; W’15Wh
CCI 3
zinc ammoniate ethylenebis Not okenr(dithiocarbamate) - poly [ethylenebis(thiuram disulphide)] [(-S.CS.NH.CHzCH2NH.CS.S-)--‘ih(NH3~~,
[ ,(-S.CS.NH.CH2CH2NH.CS.S-)
X
3-(Cbromophenyl) -l-method1-methylurea
Table 1 ( Continued )t;g
SI No. Common Name Use Chemical Name Chemical Structure Molecular Formula VI. .
(1) (2) (3) (4) (3 (6) 5z
237. metolachlor H 2~~oro-6’ethyl-~~2-methoxy-l-met C1+I,,CIW,hyl = ethyl) acet -0-toluidide
238. metoxuron
239. metribuzin
%
240. mevinphos
H 3-(3-chloro-4-methoxyphenyl) -1, I-dimethylurea
NH.C0.N(CH3),
N - N
H 4-amino 6-tert-butyld, 5-dihydro-3-methylthio-1,2,4-triazin-5- one
I 2-methoxycarbonyl-1-methylvinyldimethyl phosphate (It should be statedwhich isomer is present, for example,trun.s-mevinphos)
0
(CH30)2!OC=CH.C0.0CH~
bH3
C,H,,OQ
241. mesacarbamale I I-dimcthylamino-3, 5-xylyl methyl-carbamate
242. molinate H S-ethyl N, N-hexamethylenethiocr-bamate
353. monocrotophos I dimethyl (E)-1-methyl-2-(methylcar-bamoyl) vinly phosphate
244. monolinuron
L 245. monuron‘A
216. MSh4A H methylarsonic acid
317. nabam
H 3-(4-chlorophenyl)-1-methoxy-l-methylurea
H 3-(4-chlorophenyl)-1, 1-dimethylurea
F disodium ethylenebis (dithiocar-bama te)
\NC0.SC2H5
C,H,,NOS
II(CH30)2po\ ,H
CH 3/c=c\C0.NHCH3
c,H14N05P
C,H,,ClN,O,
cl ----($- NH.CO.N(CH~)~ C9H11C’N20
CH, - N H - C S - S N aI C&N2N&CH2-NH-CS-SNq
Table 1 ( Continued ) t3
Chemical Structure Molecular FormulaEWI51 No. Common Name IJse Chemical Name
( ’ 1 (2) (3) (4) (5). .
(6) 5;if
‘_-is. naled I 1,2-dibromo-2,2-dichloroethyldimethyl phosphate
3JY. a@o-naph-thaleneaceti~ acid P 2-( 1 -naphthyl) acetic acid
250. naptalam
251. neburon
252. niclosamide
N-1-naphthylphthlamic acid
H l-butyl-3-(3,4-dichlorophenyl)-1-methylurea
M 5-chloro-N-(2-chloro-4-nitrophenyl) =salicylamide
?IBrCI,CCHOP(OCH,)‘i
Qr~H2m60.0H
a.-& YH3NH.CO.N(CH& CH,
FCl’
OH
02NeNH-! Q
\Cl Cl
C12H1002
C1sHnN03
253 nilrol”err
254. noruron
255. (ml(!lhoal(!
H
I
7.56. oxatjazon H
&.d
2.57. exam yl I
2, 4-dicMompbenyl 4-nitnrphcnyl =. .ether
1, l-dimcthyl-3-(perhydro-4, 7-rnclhano = indcn-5-yl) urea
0, O-dimethyl S-rr]ethylw-barnoylethyl phosphorothioa!c
N, Ndmtbyl-2-metifi6timoylo~.. imirto-2-(rnethyithio) +wktamide
.“
‘ c1
m t4HC0.N(CH3)2 C13H22N20
oII C+ ~2N0415
c&f3NHco.(342sp(0(3+ 3)2,
(CH3)3L 0 0
(Y
0CH(CH3) ;
.“o’-
C15H19C12N@3
N—N\–/.’ “
cl
(CH3)2NW.C=N0.C0. NHCH3. C7H13N303S
!CH s
2-hydroxethyldirrrethylammoniurn 5-&l, 6&hydr0-@o-phU@pyTidaZin-4-yloxamate
of~ ~~ . C“H’’BrTv
NH+-COOH.(CFQ N-CH2 CH2UH
O“”*
Ji-4
f’J
Table 1 ( Conthwd ) . mQe
S1 N(I. {;olimlon Nnme Usex
Chemicrd Name C%emitad Structure Molecular Formuln .,m
(1) (q
oxine-qper exintKu
260. ox ywrboxin
261. oriydemetrm meUryl
262. ox ylkrorfcn
(3) [4)
], bis (quirroli n-t+ oh[o) copper or cuprictkpinolimxide
F 5, 6dlhydrrK2-melhyl-1, 4-oxathi-in-3-carboxanilide 4. 4dloxide
A S-2-ethylsulphinylelhyl[ thyl phosplrorilthioste
O, O-dime =
H 2-chioru-alfia, alpha, alpha, -@i-fluoro-p-tolyl-3-ethoxy-4- nitrophenjtether
“-:fi
“ (CH30)2PSCH2CH2 SC2HS
/ O-CH ~-CH3
F3C -cya-””,cl
(6)
Clotl#uN202
C6H],504PS~
C15111@5N04
263. paraquat H l, l’-dimethyl-4,4’-bipyridinium[It should be statedwhich anion is presenb for instance, paraquat dichloride or paraquat bis (methyl sulphate)]
264. parathion AI
0, 0-diethyl 0-4-nitrophenyl phos-phorothioate
265. parathion methyl A 0, 0-dimethyl 0-4-nitrophenyl phos-I phorothioate
2 6 6 . pehulate II .v-propyl butyl (ettiyl) thiocarbamate
267. pendimethalin H
268. permethrin I
N-l (l-ethylpropyl)-2, 6-dinitro-3, 4-xylidine
3-phenoxybenzyl (IRS)-&s-from-!-( 2 , 2-dichlorovmyl)-2, 2- dimethyl-cyclopropanecarboxylate
Cl&l4N%~
C9H,,-,N05PS
C,o%WSCH3(CH2)3-‘I’C0.SCH pCp H,
C2H,
tl
E. .5P
5%
S1No. Common Name use Chemical Name Chemical Structure Molecular Fonda ~..
(1) (2) (3)
269. phenothnn
270, phenthoate
VI9 271. phorate
(4) (5) (6) G
x
3-phenoxyhenzyl (UK-)-ciWwr.\- c:Jt~~o~Chrysanthernate
A ethyl 2-dimethoxythiophosphorylihio-I 2-phenylacetate or s-iJlpilli-
cthoxycsrbonylberizyl 0, CJ-dimcthylphosphoroc!ithioate
I 0, O-diethyl S-ethylthiomethyl phos-phorodhhioate
272. phosdone A S-6-chloro-2,, 3-dihydm-2~xobenz =I oxazol-3-ylglelhyl 0, 0- diethyl phos -
phomcthhioate
273. phosmet I O, Odimethyl S-phthalimidomeihylphosphorodithioate ,
$
(CH30)2 PS:H.C0.0C2H5 C1lH170.iPs~
O/\ If
(C2tiS0)2f%CH2SC2H5
C7HI ~02PS2
c1 00
‘cl-C12H15CIN04PS2
/IY ‘;
\’N– CH2SP(OC2H5)2
o
a
s
‘/ II
IN-cH#w3cH3)~
\
o
b-..
r)
——
--—,
..._..,____-w
,,,!.!
6 /\I
A,
xA
“
0
——
Table 1 ( Continued ) tl
Chemical Name t’hemical Structure Molecular Formula 8. .SI No. Common Name Use
(1) (2) (3)
279. pindone R
2 8 0 . piperonyl butoxide I
281. piperophos H
3
282. pirimiphos methyl A 0-2-diethylamino-6-methylpyrimidiI n-4-yl-0, 0-dimethyl phos-N phorothioate
283. pretilachlor H
(4)
‘I-pivaloylindan-1, 3-dione
(5) (6)F
0 3
CO.C(CH &C14H1403
2-Pbutoxyethoxy) ethyl ~-P~OPY~ =’ CH,(CH~)~OCH+H,OCH, CH,OCH,piperonyl ether
CHdCHdz
S-2-methylpiperidinocarbonylmethyl0, 0-dipropyl phosphorodithioate
c
I:N-CO.CH ,SP(OCH 2CH2CH 3)2
‘CH,
2chloro-2’, 6’-diethyl-N-(2-propoxy= ethyl) acetanilide
C 2H5
284. prochlcmw
285. profenofos
286. prometiync
287. propanil
uw
288. propargite
F l-fWpropyl-iV-[2-( 2,4,6 -trichloKI =phenoxy) cthvl~ carbamoylirnidazolc
I 04-bmmo-2+tiflrophenyl O-e(hylS-propyl phosphorothioale
H 2, Mis (isopropylamino) -6-methyl-thio-1, 3, Mriazinc
H 3’, ~’dichkJropKipiOnSnilidc
A 2-(4-tert-butylphenoxy) +30hexylprry+myl Sulphk?
-P’-‘:”’)*CH3c’/\ c,y0,NCH2CH Zo
N
L>I c1n
c@l@3N30~
Qe, / \ o!-OCZHS
kCH2C2H3
cl
CH3S
Y%
K.NHCH(Cti& c~(,H19N5s
N/‘f’
iJHCH(CH3)2
G
(:J-l@7N0
c,”/\ NH.C0.CH2CH3
c’‘f(CH3)3
““Q‘/’
\I C~91_lZ40@
o
cl’OSO.0CH2C5CH
Table 1 ( Continued ) #z
Sl No. Common Name Use Chemical Name Chemical Structure Molecular Formula . .
(1) (2) (3) (4) (5) (6)
8CH3CHzNHPO\ , H C,ob0N04PS
c=cCWCH/
3 ‘CO.OCH(CH&
5x
289. propetamphos I isopropyl (3-[ethylamino(methoxy) =phosphinothioyloxy] isocrotonate
290. propham
291. propiconazole
292. propineb F polyme’ric zinc propylenebis(dithiocarbamate)
293. propoxur I 2-isopropoxyphenyl methylcarbamate
294. propyzamide H 3,5-dichloro-N-( 1,ldimethylpropynyl) = benzamide
H isopropyl carbanilate or isopropylphenylcarbamate
F (A)-l-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2- ylmethyll-l-H-1,2,4-triazole
NH.CO.OCH(CH&
CH, (CH 2)2
C,&dO2
CH3I
[-S.CS.NHCH2CHNHCS.S.Znw] x (C5H&%Znh
O.CO.NHCH 3
O.CH(CH 3)2
295. prothoate
296. prynachlor
297. pyracarbolid
298. pyrazon (chloridazon)
299. pyrazophos
A . 0 , O-diethyl S-isopropylcarbamoyl-methyl phosphorodithioate
S
(c”3),C”N”co.c”,s~(*c~“~)~
CH3, AH-C-CH
H 2-chloro-N (1-methylprop-2-ynyi)acetanilide N\CO_CH Cl2
F 3, 4-dihydrod-methyl-2ff-pyran-j-carboxanilide
H 5-amino-4-chloro-2-phenylpyridazin-3(2-)-one
CH3 CH20.C0
F ethyl 2diethoxythiophosphorylo~~ - jmethyl = pyrazolo [l, S-a] pyrimldme-6-carboxylate
CH3
C,H,,NO&
C,,H,,CINO
St No. Common Name
(1) (2)
300. pyrethrins (the term is usedcollectively for 6 insecticidalconstituents, cinerin I, cinerin II,jasmolin I, jasmolin II,pyrethrin I, andpyrethrin II
301. pyrinuron
1Jse Chemical Name
(3) (9
cinerin I-(lS’)-3-[(Z)-bul-2-enyl]-2-methyl-4-oxocyclopent-2-enyl (lRj-trans-chrysanthemate
cinerln II - (lS)-3-[(Z)-but-2-enyl]-2-methyl-4-oxocyclopent-2- enyl (lR)-trans-3-i(E)-2-methoxycarbonylprop-1 enyl]-2,2-dimethylcyclopropanecarboxylate
jasmolin I- (lS’)-2-methyl-4-oxo-3-[(Z)-pent-2-enyl] cyclopent- 2-enyl(lR)-rruns-chrysanthemate
jasmolin II-(CT)-2-methyl-4-oxo-3-[(Z)-pent-2enyl) cyclopent-2- e n y l(lR)-lrunsd-[Q-2methoxycarbonylprop-l-enyll-2,2- dimethylcyclopropanecarboxylate
pyrethrin I- (PC)-2-methyl-4-0x0-3-[(.Z)-penta-2, 4dienyl] cyclopent-2-enyl (lR)-trans-chrysanthemate
pyrethrin II-(2-methyl-loxo-3-[(z)-penta-2, 4dienyl] cyclopent-2-enyl(JR)-truns-3-[(E)-2-methoxycarbonylprop-I-enyl]- 2,2dimethylcyclopropanecarboxylate
R l-(4-nitrophenyl)-3-(3-pyridylmethyl)urea
Chemical Structure Molecular Formula fz
Cl-l2 “NH-CO-NH
yu. quintmcne (1’CNSJ
u,-J 305. rcwtcthrin
Ii fi-chl oro-3-phcl]~lpy ridazil]-4-yl .$-octyl Ilrioca rhona [C
I
b
1
1
cl‘r’,K N
bil I\
CH3(CH2)7 Scoo /(), O-die[hvl O-auirmxdin-2-yl ph{N- 0phorolhimk “
O@CH2CH3)2
N02 .c1ocl
0
\I
c1 clc1
fRS~-ci\-
Clul [2f(:lN .()-s.-
C121115N203PS
C(,CIJQ
( ‘. .il..,,~l
(CH3)2C=CH
.H~c0”0cH2 ~ ~CH3 o
c“’ \ /
CH s
&=CHZ/
Ht1“
0-’-’%-’
CH30..
6CH3
--3
i
Table I ( Confinrrd )E
Sl No. Common Name 1 ‘se Chemical Name Chcmiml Structure Molecular Formula E. .(‘1 121 3)
L
P
OH
309. sethoxydim H (*)-24 I-ethoxyiminobutyl)-5-[2-(et OCH 2CH3hylthio) =propyI]-3- hydroxycyclohex-2 enom 0 !J
&CH,),CH,
CH3
I CH3 CH ,&HCH, OH
310. simazine H 2-chloro-4, 6-bis (ethylamino)-1,3,5-triazine
CpHSNH y,“;-(“’ C7H12CINS
“‘\ N
‘r’NHC2H5 :
2 311. sirmate (dichloromale) Ii 3, 4-dichlorobenzyl methyl carbamatc CH3 NH.CO.OCH 2
312. strychnine R strichnidin-IO-one
313. sul fometuron
C’-‘3H 2-[3-(4, 6-dimethylpyrimidin-2-)‘I)
urei = dosulphonyl] benzoic acid
Table 1 ( Conlinueri )
S1No. Common Name [kc Chmnical Name Chemical Struclure Molccul;w FormuliI
(1) (q (3) (4) i: (6)
Ss
314 Sullr)kp
315. sulphnxiclc
316. SU@phOS
317. 2.4, 5--r
318. ‘r(x (S(dhJti dt)
,4 0,0,0’,0’ -tcm]clhyldithiopyrnphospha[c
(C2H50)2kk*2Hd2
I l-nlcthyl-2<3,4 -mcthylcncdit>x? }jt]l.~;--.~ CH2 CHMe.SO(CH2)7Me
CJ,JI@$nyi) ~thyl octyl mlphbxidr
I
H
H
O-ethyl ()-4 -meth!’llhio@cnyl > i
-c)-
:~H,s ”/\ f
pruplyl phosphomdiihinate ~H2C2%—
0C2H5
cl
(2, 4 Mrichkmrpherroxy) arxtic acid
, t~
~, i \ ~~”,~~ (’j”.—
clsodium Iridrloroacelate
c13C.C0.0-Na+
C9H5C1303
31Y. tebuthiuron H l-(5tert-butyl-1,3,4-thiadiazol-2-yl)-1,3dimethylurea (CH3)3C y Sk ~~.NHCH3
320. tecnazene F 1,2,4,5-tetrachloro-3-nitrobenzene
CyH16N,0S
C,HCI,N02
321. temephos
322. TEPP
323. terbacil
324. terbuthyl = azine
I U,O,O’,O’-tetramethyl 0 , O’-thiodi-p-phenylene his (phosphorothioate)
(C”, O$)‘&_ S 0 o,~,l%,,,r,.~”
A tetraethyl pyrophosphate
H 3-reti-butyl-khlorod-methyluracil
0
H 2-rert-butylamino-4-chlorod-ethylamino-l, 3,5,-triazine
NHC(CH 3j3
NHCzH5
C&oO,f2
CyH,,CIN,O,
CyH,,CIN5
t;:E. .5z
Table 1 ( Continued )FiE
Sl No. Common Name Use Chemical Name Chemical Structure Molecular Formula (II. .
(1) (2)
32.5. terbutryne
326. tetrachlor = vinphos
327. tetradifon
328. tetramethrin
H 2-krt-butylamino-4-ethylamino-6-methylthio-1,3, S-triazine
(3
@HsS y N y’ NHC(CH3)3,
N AN
YNHC~H~
0
I (Z)-2-chloro-1-(2,4,5-trichlorophenyl) Cl-a-/ \ Cl= vinyl diiethyl phosphate
A -I-chlorophenyl 2 4 S-trichlorophenyl Clsulfone
I 3,4, 5,6-tetrahydrophthalimidomethyl(IRS)-cis-trans- chrysanthemate
(6)
C,oH,,W
‘bx
329. thiabendazole F 2-(thiazol-4-yl) bcnzimidazole
330. thiobencarb
331. thiocyclam
332. thiometon
333. thionazin
334. thiophanate methyl
335. thiram
f-1 S-4-chlorobenzyl d i e t h y l (thiocar-bamate)
.I N, A’-dimethyl-1, 2 , 3-trithian-5-ylamine
A S-2ethyhhioethyl0, Odimethyl phos -I phorodithioate
IN
O,O-diethyl 0-pyrazin-2-yl phos-phorothioate
F dimethyl 4, 4’-(0-phenylene) bis (3-thioallophanate)
F bis (dimethylthiocarbamoyl)phide or tetramethylthiuramphide
disul-disul-
SII
(C”SO),PS(C”~,SC~“S
S
-? O!(OC,H,),
NHCS.NHCO.OCHS
NHCS.i4HC0.0CHI
(CH,),NCS.SI
(cH~)~NCS.S
~,&7N3S
G%W3
C’,H,&S,
Table 1 ( Continued ) EX
SI No. Common Name IJse
(1) (2) (3)
336. tolclofosmethyl F
337. toxaphene A1
338. triadimefon F
E 339. triadimenol F
340. tri-allate 1-I
341. triazophos 1
Chemical Name
2,6,dichloro-I?-tolylphosphorothioate
O,O-dimethyl
A reaction mixture of chlorinated cam-phenes containing 67 to 69 percentchlorine
1-(4-chlorophenoxy)-3,3dimethyl-l-(lif-I, 2,4-triazol-1-yl) butanone
l-(4chlorophenoxy)-3,3dimethyl-l-(UT-1,2,4-triazol-l-yl) butan-2-01; it isa mixture of 2 diastereoisomeric forma
S, 2, 3, 3-trichloroallyl di-isopropyl(thiocarbamate)
0, 0-diethyl 0-1-phenyl-W-1, 2, 4-triazol-3-yl phosphorothioate
Chemical Structure Molecular Formula iz. .
CHS O$OCH&
STRUCTURE UNKNOWN
OHI.
Cl 0-CH-CH.C(CH&I
/N\
d-!!f
[(CH3) CH& NC0.SCH,k=CC12
t:‘OP(OC.H,),II
CtdI,nCI, (approx)
C&,&I,NOS
342. Tributyl phosphorotrithioite H tributyl phosphorotrithioite
343. trichlorphon I dimethyl 2, 2, 2-trichloro-l-hydroxyethylphosphonate
344. triclopyr
345. tricyclazole
346. tridemorph
347. trifluralin
348. triforine
II 3, 5 , 6-trichloro-2-pyridyloxyaceticacid
I:Cl3 CCHP(OCH&
I
Cl OCH,CO.OH
F S-methyl-l, 2,4-triazolo [3, 4- b] ben-zothiazole
Icu_ CH3
F 2,6, dimethyl-4-tridecylmorpholine /-(CHS -(CH 2), 2 - N, 0
/
C12H27PS,
C,H&I,O,P
C,H&S
H 2, Gdinitro-N, N-dipropyl-4-trifluoro= C,,H,,F&O,methylaniline 2-CH 2-CH,)2
‘ N O ,
Cl, CFHNQCHO
F 1, 4-bis (2 , 2 , 2-trichloro-l-for-mamidoethyl) = piperazine 0
NI
CI,CCHNHCHO
Table 1 ( Concluded ) t;
Chemical Structure Molecular Formula ESI No. Common Name Use Chemical Name
(1) (2) (3) (4) (5). .
349. validamycin F &(I, 3, 4/2, 6)-2, 3dihydroxy-6-hydroxymethyl-4-[(lS, 4R, 5% 69 -65, 6-trihydroxy-3-hydroxy=methyl-cyclohex-2-enylamino] cyclohexylbeta-D-glucopyranoside
350. vamidothion
351. vernolate
35’.i vinclozolin
A 0, 0-dimethyl S-2-(l-methylcar-I bamoylethylthio) ethyl phos-
phorothioate
H S-propyl dipropylthiocarbamate
F 3-(3 , 5dichlorophenyl)~S-methyl-5vinyl-l, 3-oxazolidine-2,4- dione
OH
HO 0
OH
CH3I
CH3NHC0.CHSCH 2CH 2SP(OCH 3)2
353. warfarin
354. zineb
‘355. Gram
3
R 4-hydroxy-3-(3-oxo-1-phenylbutyl)coumarin
F Zinc ethylenebis (dithiocarbamate)(polymeric) (the chemical structure isnot yet fully known)
F zinc bis (dimethyldithiocarbamate)
C19H1604
E. .tx
IS 885 : 1994
ANNEX A( Clause 5.2 )
PESTICIDES NOT REQUIRING COMMON NAMES
Sl Name ofpesticideNo.
1. Aluminium phosphide
2. Ammonium sulphamate
3. Barium carbonate
4. Barium fluorosilicate
5. Barium polysulphide
6. Boric acid
7. Cadmium based compounds
8. Calcium arsenate
9. Calcium cyanide
10. Carbon disulphide
Sf Name of PesticideNo.
28. Ethyl mercury phosphate
29. Ethylene dibromide
30; Ethylene dichloride
3 1. Hydrogen cyanide
32. Hydrogen phosphide
33. Lead arsenate
34. Lime sulphur
35. Magnesium phosphide
36. Mercuric chloride
37. Methyl bromide
11. Carbon tatrachloride 38. Methyl mercury chloride
12. Copper acetoarsenite (Paris Green) 39. Methylene chloride
13. Copper arsenate
14. Copper cyanide
15. Copper hydroxide
16. Copper naphthanate
17. Copper oxychloride
18. Copper sulphate
19. Cuprous oxide
20. y-dichlorobenzene
21. Dusting sulphur
22. EDCT mixture
40. Nickel chloride
41. Nicotine. sulphate
42. Pentachlorophenol
43. Phenyl mercury acetate
44. Phenyl mercury chloride
4.5. Phenyl mercury salicylate
46. Phenyl mercury urea
47. Phosphorus paste
48. Potassium cyanide
49. Sodium cyanide
23. E t h o x y e t h y l c h l o r i d emercury 50. Sodium flouroac
24. Ethyl fonnate 51. Sodium fluorosietate
25. Ethyl acetatemercury 52. Sulphurlicate
26. Ethyl bromidemercury 53. Tar acid
27. Ethyl chloridemercury 54. Zinc phosphide
6 8
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This Indian Standard has been developed from Dot : No. FAD I ( 4009 ).
Amendments Issued Since Publication
Amend No. Date of Issue Text Affected
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