Remember BASF’s bed bug prevention pitch?
The research is out and worth a close reading, not only because it is the anticipated report on the effectiveness of old dry residues of chlorfenapyr against bed bugs, a subject that sets off our collective anxieties about using pesticides preventatively, but it’s the first study of chlorfenapyr’s effectiveness against pyrethroid-resistant bed bugs.
Romero, Alvaro, Michael F Potter, and Kenneth F Haynes. 2010. Evaluation of chlorfenapyr for control of the bed bug, Cimex lectularius L. Pest Management Science. doi:10.1002/ps.2002
Chlorfenapyr is what is called a pro-insecticide in that it does not become active (toxic) until it is metabolized by the bed bug itself after absorption. It belongs to a class of pesticides called pyrroles.
It works on bed bugs as follows:
The active metabolite of chlorfenapyr (AC 303,268) inhibits the ion transport system of the respiratory chain in mitochondria, preventing the production of the energy molecule adenosine triphosphate (ATP), so leading to insect death.
Yes, but let’s not be deterred.
Cell energy being the operative concept, if one wanted a handy simplification (and one does!), it seems to me they get tired and then they die:
Typical symptoms of chlorfenapyr intoxication in bed bugs include sluggish movements, prostration and limited responses upon contact stimulus (Romero A, personal observation). Such symptoms may be less apparent in commercial practice, and users should understand that bed bugs treated with chlorfenapyr succumb more slowly compared with some other insecticides.
Thank you for that image, Dr. Romero.
This is unlike the nerve-acting pyrethroids which make bed bugs hyperactive. Here let’s note for those who are just joining us that pyrethroid resistance is depressingly widespread (also see) and so much at the center of our troubles.
On this note, the authors raise our interest a bit:
It has been suggested that resistant arthropod populations with enhanced monooxygenase activity might have increased sensitivity to chlorfenapyr (a case of a phenomenon known as negative resistance), because pyrethroid resistance can be caused by detoxification by the same enzymes (P450 monooxygenases) that activate the pro-insecticide chlorfenapyr.
Only to pour cold water a sentence later:
In the present study, the similar rate of mortality caused by chlorfenapyr to all strains, regardless of their pyrethroid susceptibility status, suggests that the presence of pyrethroid resistance in bed bugs might not limit (or enhance) the effectiveness of chlorfenapyr.
If only pyrethroid resistance were good for something. But they found no evidence of this negative resistance (because it would be too cool for words and we should know by now such gifts are not allowed us in this great contest with our enemy).
Let’s get back to insect death, by all means.
Comparison of two chlorfenapyr formulations
Phantom is formulated chlorfenapyr and there is an aerosol and a liquid concentrate:

Toxicity of chlorfenapyr formulations (Phantom aerosol and Phantom SC), Romero et al. (2010), Pest Management Science
Yes, the obnoxious CIN-1 strain.
It’s very interesting that the aerosol is faster as a dry residue as well.
Directly sprayed bed bugs (aerosol formulation)
Direct sprays with the aerosol caused 30% mortality to both pyrethroid-resistant strains within 4 h (data not shown) and about 50% mortality in 24 h. In contrast, direct sprays of the water-based formulation took at least 3 days (WOR-1) or 5 days (CIN-1) to cause 50% mortality. Direct sprays of the blank aerosol (formulation without chlorfenapyr) killed 25% of individuals within 4 h, which indicates that some formulation ingredients also have some contact activity. Insecticides that kill bed bugs upon contact are widely used by pest control companies because they can quickly suppress populations and provide some relief to their customers.
And:
Bed bugs from strains CIN-1 and WOR-1 showed no avoidance of surfaces treated with the chlorfenapyr aerosol.
No avoidance “presumably lessens the potential spread of bed bugs to adjoining areas.”
Dry residues (of liquid formulation)
The LT50 of (time necessary to kill 50% of individuals) for CIN-1 bed bugs exposed to a 4-month-old dry residue deposit of Phantom (liquid formulation) was 4.6 days (and it was 4.8 days for fresh deposits), which means that the 4-month-old dry residue was just as toxic as a fresh deposit. The LT90 was 8.8 days.
In other words, chlorfenapyr is that rare thing, an effective (if slower) residual pesticide against bed bugs. What challenges are tied to its slow action (continued feeding and egg-laying?) have to be set against, well, that it works.
The authors note the potential preventive value of these findings:
The ability of chlorfenapyr to remain effective over an extended period of time is encouraging because bed bugs that are not sprayed directly may still succumb after residing on treated surfaces. Most insecticides available today have limited potency as a dry deposit against pyrethroid-resistant bed bugs. Dry residual action of chlorfenapyr might also aid in preventing new infestations if likely areas of infestation are previously treated.
…but recommend further study of chlorfenapyr’s residual effectiveness on various surfaces and the “suitability of prophylactic applications” — which I’m afraid leaves us where we were, with the manufacturer recommending just such a course (PDF) and prudent people urging caution.
More research please.
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This was almost the last planned post here but there will be one more. Thanks for reading. I keep a bed bug-related reading list you are welcome to follow if you are interested. Best wishes.