67747-09-5 Usage
Description
Prochloraz is a broad-spectrum fungicide that is effective against a wide range of diseases affecting field crops, fruit, turf, and vegetables. It is a protectant and eradicant fungicide, which means it can prevent the development of fungal diseases and also eliminate existing infections.
Uses
Used in Agriculture:
Prochloraz is used as a fungicide for the control of various fungal diseases in field crops, fruit, turf, and vegetables. It is recommended for use on cereals against Pseudocercosporella, Pyrenophora, Rhynchosporium, and Septoria spp., and on oilseed rape against Alternaria, Botrytis, Pyrenopeziza, and Sclerotinia spp.
Used in Postharvest Treatment:
Prochloraz is used as a dip treatment, showing good activity against storage or transit diseases of citrus and tropical fruit. This helps to extend the shelf life of these fruits and reduce postharvest losses.
Used in Seed Treatment:
Prochloraz is also used as a seed treatment to control several diseases of cereals. This helps to protect the seeds from fungal infections and ensures healthy crop growth.
Mode of action
The action of imidazoles used as fungicides or antimycotic drugs (e.g. ketoconazole) is based on the inhibition of the cytochrome P450-dependent 14a-deme- thylase activity required in the conversion of lanosterol to ergosterol[4], an essential component of fungal cell membranes. The molecular basis of this inhibition is the presence of an imidazole moiety that interacts strongly with the iron atom of cytochrome P450. The binding is fairly unspecific and thus imidazole fungicides also inhibit the activities of a broad spectrum of other cytochrome P450-dependent enzymes, including key enzymes involved in biosynthesis and metabolism of steroids, e.g. CYP19 aromatase[5].
Physiological effect
Prochloraz is a currently used imidazole fungicide that shows multiple mechanisms of endocrine action in vitro. It is a novel endocrine disruptor that is mechanistically interesting as it elicits dual mechanisms of action and acts as an antiandrogen both by blocking AR, like the well-known fungicides vinclozolin and procymidone, and by inhibiting fetal steroidogenesis like the phthalates. However, the mechanism of action of prochloraz differs from that of the phthalates, as steroidogenesis seems to be directly inhibited by prochloraz possibly at the 17a-hydroxylase/lyase level. Several of the observed in vivo effects can be explained by this disruption of fetal steroidogenesis: (i) the increased pregnancy length of the dams; (ii) the reduced testosterone and increased progesterone in male foetuses; and (iii) the feminized behaviour of adult males[6-9].
Prochloraz acted as an ER and AR antagonist as well as an aromatase inhibitor with IC50 (the concentration that induces half-maximal inhibition of activity) values of 25, 4 and 0.3 lm respectively. Furthermore, prochloraz was able to activate the aryl hydrocarbon receptor (AhR) having an EC50 (the effective concentration that induces half- maximal activation) of 1 lm. The antioestrogenic effects were evident both in a MCF7 cell proliferation assay and in an ER reporter gene assay. Although the potencies of prochloraz to antagonize ER and AR, agonize AhR, and to inhibit aromatase are relatively weak, the ability of prochloraz to act via more than one mechanism might enhance the biological effect in the intact organism, as the final response may be determined by the interactions of all pathways involved[10-12].
The in vivo effect of prochloraz is in agreement with the AR antagonism observed in vitro. Comparing the in vivo effect of prochloraz to the well-known AR antagonist vinclozolin shows that the magnitude of the response to prochloraz is within the range of 26–65% of the response to vinclozolin when organ weight changes is the selected end point. p,p’-DDE at a dose level of 50 mg/kg did not significantly reduce prostate weight, and therefore the effect of prochloraz in the Hershberger assay is intermediate to that of vinclozolin and p,p’-DDE. The in vitro transcriptional assay showed that prochloraz acted as an AR antagonist having an IC50 of 4–8 lm depending on the androgen concentration. For comparison the IC50 of vinclozolin and p,p’-DDE in our AR assay is approximately 10-fold lower, being around 0.4 and 0.3 lm respectively. Thus, compared with relations between potencies observed in vitro and in vivo for other antiandrogens, the in vivo response induced by prochloraz in the Hershberger assay was higher than predicted from the in vitro assay[8].
Toxicity
Absorption of prochloraz via inhalation, ingestion, or direct skin and eye contact may result in certain kinds of adverse reactions. Inhaling toxic fumes may cause severe respiratory irritation, sore throat, and nasal inflammation. Likewise, inhaling the hazardous substance may further exacerbate the condition of people with pre-existing respiratory disorders such as chronic bronchitis and impaired respiratory function.
Prochloraz can also negatively affect the female reproductive health too. Exposure to the harmful compound may lead to mood swings, depression, weight gain, and hot flushes as well as vaginal dryness, bloating, and early menopause. Long-term prochloraz exposure has been found to cause circulatory disorders such as increased blood clots, low blood pressure, blood vessel dilation, and white blood cell death.
The hazardous chemical can also trigger series of other systematic effects such as the onset of bone weakness, mineral imbalance, and cardiovascular damage as well as liver injury, convulsions, and gastrointestinal disturbance. The fungicide is found to seep into open wounds and abrasions as well, which in turn may lead to severe skin irritation and more serious conditions such as severe peripheral neuropathy, limb paralysis, and loss of sensation. Furthermore, direct eye contact may result in severe eye irritation and corneal injury[13].
References
Bill Carlile (28 September 2006). Pesticide Selectivity, Health and the Environment. Cambridge University Press. pp. 81–. ISBN 978-1-139-45756-9.
Kalyani Paranjape; Vasant Gowariker; V N Krishnamurthy; Sugha Gowariker (22 December 2014). The Pesticide Encyclopedia. CABI. pp. 406–. ISBN 978-1-78064-014-3.
https://sitem.herts.ac.uk/aeru/ppdb/en/Reports/536.htm
Henry, M. J. & Sisler, H. D. (1984) Effects of sterol biosynthesis-inhibiting (SBI) fungicides on cytochrome P-450 oxygenations in fungi. Pesticide Biochemistry and Physiology 22, 262–275.
Laignelet, L., Narbonne, J. F., Lhuguenot, J. C. & Riviere, J. L. (1989) Induction and inhibition of rat liver cytochrome(s) P-450 by an imidazole fungicide (prochloraz). Toxicology 59, 271–284.
Christenson, L. K. & Devoto, L. (2003) Cholesterol transport and steroidogenesis by the corpus luteum. Reproductive Biology and Endocrinology 1, 90.
Wilson, V. S., Lambright, C., Furr, J., Ostby, J., Wood, C., Held, G. & Gray, L. E., Jr (2004) Phthalate ester-induced gebernacular lesions are associated with reduced insl3 gene expression in the fetal rat testis. Toxicology Letters 146, 207– 215.
Vinggaard, A. M., Nellemann, C., Dalgaard, M., Jorgensen, E. B. & Andersen, H. R. (2002) Antiandrogenic effects in vitro and in vivo of the fungicide prochloraz. Toxicological Sciences 69, 344–353.
Vinggaard, A. M., Hnida, C., Breinholt, V. & Larsen, J. C. (2000) Screening of selected pesticides for inhibition of CYP19 aromatase activity in vitro. Toxicology In Vitro 14, 227–234.
Laignelet, L., Rivie`re, J.-L. & Lhuguenot, J.-C. (1992) Metabolism of an imidazole fungicide (prochloraz) in the rat after oral administration. Food and Chemical Toxicology 30, 575–583.
Andersen, H. R., Vinggaard, A. M., Rasmussen, T. H., Gjermandsen, I. M. & Bonefeld-J?rgensen, E. C. (2002) Effects of currently used pesticides in assays for estrogenicity, androgenicity and aromatase activity in vitro. Toxicology and Applied Pharmacology 179, 1–12.
Long, M., Laier, P., Vinggaard, A. M., Andersen, H. R., Lynggaard, J. & Bonefeld-J?rgensen, E. C. (2003) Effect of currently used pesticides in the AhR-CALUX assay: comparison between the human TV101L and the rat H4IIE cell line. Toxicology 194, 77–93.
http://pesticides.news/2017-11-15-prochloraz-toxicity-side-effects-diseases-and-environmental-impacts.html
Trade name
ASCURIT?; BTS40542?; DIBAVIT?; EYETAK?; FORTAK?; FUNCHLORAZ?; GRAIL?; MASTER?; MIRAGE?; MIRAGE? 40 EC; PORAZ?; SPORGON?; SPORTAK?; SPORTAKALPHA?; SPORTAKDELTA?
Metabolic pathway
Prochloraz is metabolised in plants and animals and degrades in soils.
The initial step in the metabolic pathway is cleavage of the imidazole ring;
the substituted ureas that result are subsequently degraded to moieties
containing a chlorophenoxy residue and the ring is hydroxylated. Residues
may be conjugated in animals and plants.
Degradation
Prochloraz is stable in water at pH 7 and 20 °C. It decomposes on
exposure to sunlight and is also decomposed by concentrated acids and
alkalis.
Check Digit Verification of cas no
The CAS Registry Mumber 67747-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,4 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67747-09:
(7*6)+(6*7)+(5*7)+(4*4)+(3*7)+(2*0)+(1*9)=165
165 % 10 = 5
So 67747-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H16Cl3N3O2/c1-2-4-20(15(22)21-5-3-19-10-21)6-7-23-14-12(17)8-11(16)9-13(14)18/h3,5,8-10H,2,4,6-7H2,1H3
67747-09-5Relevant articles and documents
Safe and reliable prochloraz preparation method
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Paragraph 0053; 0057; 0062-0065, (2019/10/01)
The invention discloses a safe and reliable prochloraz preparation method. The safe and reliable prochloraz preparation method comprises following steps: S1, etherification reaction, wherein 2, 4, 6-trichlorophenol, a liquid alkali, and dichloroethane are subjected to sealing heating reaction so as o obtain a S1 etherification intermediate; S2, amination reaction, wherein propylanmine is added, heating reaction is carried out, distillation recycling of propylanmine is carried out, and extraction is carried out so as to obtain a S2 secondary amine intermediate solution; S3, esterification reaction, wherein an acid binding agent A, and a halogenated formate are added, room temperature reaction is carried out for 1 to 3h, and filtering is carried out so as to obtain a S3 esterification intermediate solution; and S4, carbonylation condensation reaction, wherein catalyst B and imidazole are added, reflux reaction is carried out, and washing, extraction, and distillation are carried out so as to obtain prochloraz finished product. According to the safe and reliable prochloraz preparation method, the halogenated formate is adopted to replace a phosgene similar agent as a carbonylation condensation reagent, and sealing, waterless, and rectification reflux reaction conditions are adopted, so that continuous production is realized; the prochloraz total yield is high; no phosgene leakagesafety hidden trouble is caused; and the safe and reliable prochloraz preparation method is worthy of popularization.
Synergistic Active Compound Combinations Comprising Phenyltriazoles
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, (2011/07/29)
The present invention relates to novel active compound combinations comprising, firstly, at least one known compound of the formula (I) in which R1 and R2 have the meanings given in the description. and at least one further known active compound from groups (2) to (27) listed in the description, which combinations are highly suitable for controlling animal pests such as insects and unwanted acarids and also phytopathogenic fungi.
Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides
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, (2008/06/13)
The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.
