Disclosure to Promote the Right To Information

Whereas the Parliament of India has set out to provide a practical regime of right to information for citizens to secure access to information under the control of public authorities, in order to promote transparency and accountability in the working of every public authority, and whereas the attached publication of the Bureau of Indian Standards is of particular interest to the public, particularly disadvantaged communities and those engaged in the pursuit of education and knowledge, the attached public safety standard is made available to promote the timely dissemination of this information in an accurate manner to the public.

इंटरनेट मानक

“!ान $ एक न' भारत का +नम-ण”Satyanarayan Gangaram Pitroda

“Invent a New India Using Knowledge”

“प0रा1 को छोड न' 5 तरफ”Jawaharlal Nehru

“Step Out From the Old to the New”

“जान1 का अ+धकार, जी1 का अ+धकार”Mazdoor Kisan Shakti Sangathan

“The Right to Information, The Right to Live”

“!ान एक ऐसा खजाना > जो कभी च0राया नहB जा सकता है”Bhartṛhari—Nītiśatakam

“Knowledge is such a treasure which cannot be stolen”

“Invent a New India Using Knowledge”

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. 4dihydro-4+xo@w.o [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

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