Appendix 4.B Compounds to be used with CAUTION (updated September 2025)

(limited lifetime, restricted markets, etc.)

These AI:

  • have permitted MRLs in some markets, but not others and/or…
  • may have have registration in at least one major cocoa growing country
  • may have temporary (tMRLs) or strong possibility of phasing-out within coming years, but…
  • have shown demonstrable efficacy in at least one regional cocoa growing country
  • do not belong to WHO/EPA toxicity Class I
     

(i) diseases

Active ingredients MoA group EU status EU MRL JP MRL
chlorothalonil δ M5 N 0.05 0.05

(ii) insects

Active ingredients MoA group EU status EU MRL JP MRL
fenobucarb (BPMC) 1A N *ø (0.01) 0.02
MIPC, isoprocarb 1A N *ø (0.01) 0.02
diazinon 1B N 0.05  
dimethoate 1B N 0.05 0.01
fenitrothion 1B N * 0.05  
chlorpyrifos (ethyl) β 1B N 0.01 0.01
bifenthrin 3 N 0.05 0.1§
beta-cyfluthrin β,T 3 N 0.05 0.1
clothianidin χ 4A N 0.02 0.02§
imidacloprid 4A N 0.05 0.05§
thiamethoxam 4A N 0.02 0.02§
thiacloprid 4A ξ N 0.05  
novaluron π 15 N (0.05) (0.01)
pymetrozine 9B N 0.1  
teflubenzuron π 15 N 0.05 0.02
Useful especially for termite control        
fipronil Y, β 2 N 0.005 Y 0.01

(iii) weeds

Active ingredients MoA group EU status EU MRL JP MRL
2,4-D dimethylamine salt O Y * 0.1 0.01
picloram O Y 0.01 (T) (0.01)
paraquat, diquat δ D N 0.05 (T) 0.05

(iv) stored produce etc.

Fumigants *** MoA group EU status EU MRL JP MRL
methyl bromide μ 8A N 0.01 & US:
(as inorganic bromide ion)     70.0 50.0
Rodenticides *** (anti-coagulant – see text)      
brodifacoum, 3 N (0.01) (0.01)
bromadiolone, difenacoum 8A N (0.01) (0.01)
warfarin (coumaphene) 24 N (0.01) (0.01)
Key  
* High residue levels have been found in imported produce to the EU and/or Japan (**: >10 cases since 2008)
*** High mammalian toxicity: to be used only by qualified personnel
§ Now to be tested in Japan after removal of shell (testa); Japan MRLs in brackets assumed to be at default.
M Current moratorium on use in the EU due to suspected bee toxicity
α No MRL given in Japan and copper is exempt in the USA
µ Metalaxyl includes mixtures of all constituent isomers including metalaxyl-M (sum of isomers)
β Registered (widely used) for cocoa pod borer control in Indonesia
ξ Cyano-substituted neo-nicotinoid
δ Includes deltamethrin and tralomethrin (as total)
π Usually sold as a mixture (co-formulated with a pyrethroid)
σ Mostly for stump treatments in CSSVD eradication
   
β Chlorpyrifos is banned in Europe and persistent enough to present significant residue risk. Registered for cocoa pod borer control in C. d’Ivoire and Indonesia.
T Toxicity of AI in class 1b, but still registered in some jurisdictions
Y Fipronil (sum fipronil + metabolites). Five degradation products are known, depending on the mode of break-down: fipronilsulfone, fipronil-sulfide, fipronil-desulfinyl, fipronil-amide, and fipronil-detrifluo-romethyl-sulfinyl. Fipronil is not permitted for use as spraying in the EU or USA and has generally permitted only for targeted applications such as baiting, in-furrow and seed treatments; however, it has been registered for spraying CPB (above) and mirids in 2 African countries.
ε Use of pirimiphos methyl in cocoa is no longer defended by Syngenta; zero tolerance (i.e. LOD) for this AI in Australia.
δ US MRL of 0.05
χ Clothianidin appears to have had little use in cocoa to date, but for residue analysis note: Naeun et al (2003) [1]
μ Restricted under the Montreal Protocol; to be phased out by EPA (mostly by 2017)
π Usually sold as a mixture (co-formulated with a pyrethroid)
ø P pesticides are used outside the EU but for which no toxicological data and no MRLs have been notified for inclusion in 396/2005/EC Annex III (neither by the member states, in the form of import tolerances, nor by third countries). Such compounds may have a clear purpose outside Europe (e.g. fenobucarb: which is widely used for control of hemipteran pests of rice in Asia, and has also been applied to cocoa in certain countries).

[1] Nauen R, Ebbinghaus-Kintscher U, Salgado VL, Kaussmann M (2003) Thiamethoxam is a neonicotinoid precursor converted to clothianidin in insects and plants. Pesticide Biochemistry and Physiology 76: 55-69. https://doi.org/10.1016/S0048-3575(03)00065-8