Triclabendazole Powder
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Triclabendazole Powder

Triclabendazole Powder

1.General Specification(in stock)
(1)Injection
Customizable
(2)Tablet
Customizable
(3)API(Pure powder)
PE/Al foil bag/ paper box for Pure powder
HPLC≥99.0%
2.Customization:
We will negotiate individually, OEM/ODM, No brand, for secience researching only.
Internal Code: BM-1-092
Triclabendazole CAS 68786-66-3
Analysis: HPLC, LC-MS, HNMR
Technology support: R&D Dept.-4

Shaanxi BLOOM Tech Co., Ltd. is one of the most experienced manufacturers and suppliers of triclabendazole powder in China. Welcome to wholesale bulk high quality triclabendazole powder for sale here from our factory. Good service and reasonable price are available.

 

Triclabendazole powder is a high-efficiency benzimidazole deworming compound. It's currently the go-to raw material for treating liver fluke disease, lung fluke disease, and Fasciolopsis buski infections worldwide. Compared to traditional deworming agents like avermectin and ivermectin, it offers irreplaceable advantages. Bloomtechz has been deeply involved in high-end pharmaceutical raw materials, veterinary active ingredients, and fine intermediates for years. With mature synthesis processes, standardized production systems, and flexible capacity layouts, we've built a high-quality exclusive supply system for this product, breaking the barriers to global premium raw material supply.

 

 Produnct Introductionproduct-15-15

Additional information of chemical compound:

Triclabendazole Additional | Bloomtechz

 
Our Product
 
Triclabendazole Powder | Bloomtechz
Triclabendazole powder
Triclabendazole Tablets | Bloomtechz
Triclabendazole tablets
Triclabendazole Injection | Bloomtechz
Triclabendazole injection

Triclabendazole +. COA

Triclabendazole COA | Bloomtechz

 

Triclabendazole Information | Bloomtechz

Manufacturing Information

Common synthesis methods
 

Triclabendazole powder is a benzimidazole antiparasitic drug mainly used to treat fascioliasis caused by liver flukes. The synthesis method involves multiple key steps, including nitro reduction, cyclization, methylation, etc. The following are several common methods for synthesizing trichlorobenzothiazole:

Method 1: Synthesis route starting from 4-chloro-5- (2,3-dichlorophenoxy) -2-nitroaniline

Nitro reduction:

Raw material: 4-chloro-5- (2,3-dichlorophenoxy) -2-nitroaniline.
Reaction conditions: In an organic solvent, trichlorosilane is used as a reducing agent for the reduction reaction to obtain the first intermediate compound (4-chloro-5- (2,3-dichlorophenoxy) -1,2-phenylenediamine), which is directly added to the next reaction step without separation.
Features: This step improves the nitro reduction method, reduces equipment requirements, and simplifies post-processing steps.

Ring closing reaction:

Raw material: First intermediate compound.
Reaction conditions: In the presence of potassium hydroxide, a cyclization reaction occurs with carbon disulfide to prepare the second intermediate (5-Chloro-6- (2,3-dichlorophenoxy) -2-Thiobenzimidazole).
Features: By changing the feeding sequence, the release rate of hydrogen sulfide is controlled, reducing the impact on the environment.

Methylation reaction:

Raw material: Second intermediate.
Reaction conditions: Under the catalysis of DBU (1,8-diazabicyclo [5.4.0] undec-7-ene), it undergoes methylation reaction with dimethyl carbonate to ultimately produce trichloropyrazole.
Features: Using dimethyl carbonate instead of dimethyl sulfate or iodomethane as a methylating agent is more environmentally friendly.

Technological advantages:

The total yield of this process can reach 55% to 60%, and the various indicators of the obtained triclabendazole meet the standards of the European Pharmacopoeia.
The process has improved the nitro reduction and cyclization steps, simplified the operating procedures, and increased the yield, which has great industrial application prospects.

Triclabendazole Chemical | Bloomtechz

Method 2: Synthesis route starting from 3,4-dichloroaniline

01/

Acylation reaction:
Raw material: 3,4-dichloroaniline.
Reaction conditions: Acylation reaction occurs with acetyl chloride or acetic anhydride in acetic acid to produce 3,4-dichloroacetanilide.

02/

Nitrification reaction:
Raw material: 3,4-dichloroacetanilide.
Reaction conditions: In the presence of sulfuric acid, nitration reaction occurs with a mixed acid of nitric acid and acetic acid to produce 4,5-dichloro-2-nitroacetanilide.

03/

Hydrolysis reaction:
Raw material: 4,5-dichloro-2-nitroacetanilide.
Reaction conditions: Hydrolysis reaction occurs in the presence of potassium carbonate and water to produce 4,5-dichloro-2-nitroaniline.

04/

Etherification reaction:
Raw materials: 4,5-dichloro-2-nitroaniline and 2,3-dichlorophenol.
Reaction conditions: Etherification reaction occurs at high temperature in the presence of potassium carbonate and phase transfer catalyst (such as tetrabutylammonium chloride) to produce 4-chloro-5- (2,3-dichlorophenoxy) -2-nitroaniline.

Discovering History

 

The development history of triclabendazole powder can be traced back to the mid to late 20th century. Its research and development, application, and optimization process reflect the close integration of chemical synthesis technology and parasitic disease prevention and control needs. The following is a detailed introduction to its development process:

 

Research and Development Background: The Urgent Need for Parasitic Disease Prevention and Control

In the mid-20th century, liver fluke disease (caused by liver flukes) was widely spread in animal husbandry, resulting in slow growth, decreased milk production, and even death in ruminant animals such as cattle and sheep, causing huge economic losses to global animal husbandry. At the same time, although cases of human infection with liver flukes are rare, the misdiagnosis rate is high, treatment is difficult, and efficient drugs are urgently needed. At that time, traditional deworming drugs such as praziquantel and albendazole had limited effectiveness against liver flukes and had resistance issues, prompting scientists to search for new antiparasitic compounds.

Triclabendazole Development Background | Bloomtechz

Research and Development Breakthrough: Exploration of Benzimidazole Derivatives
 

1. Compound screening and structural optimization
In the 1970s, researchers discovered through high-throughput screening that benzimidazole compounds had potential activity against flukes. Further structural modifications indicate that introducing a methylthio group (- SCH3) at the 2-position of the benzimidazole ring and connecting a chlorinated phenoxy group at positions 5 and 6 can significantly enhance the killing effect on liver flukes.

 

In the 1980s, Swiss company Ciba Geiger (now Novartis Group) successfully synthesized trichloronazole, with the chemical name 5-chloro-6- (2,3-dichlorophenoxy) -2-methylthio-1H-benzimidazole, a molecular weight of 359.66, a melting point of 175-176 ℃, and a white crystalline powder appearance.

 

2. Analysis of the mechanism of action
Research has found that snalvbendaz exerts its insecticidal effect by interfering with the energy metabolism of insects
Inhibiting the insect's berberine reductase system, blocking anaerobic glycolysis, leading to energy (ATP) depletion;

 

Interfering with the microtubule structure of the parasite, inhibiting protein synthesis, and causing paralysis and death of the parasite;
It has a strong killing effect on both the larvae and adults of Fasciola hepatica, and the parasite is quickly eliminated after medication, reducing host tissue damage.

Clinical Application: Expansion from Animal Husbandry to Human Medicine

 

Triclabendazole Animal Husbandry | Bloomtechz

1. Wide application in animal husbandry

In the late 1980s, Triclabendazole was officially approved for clinical use in ruminant livestock including cattle and sheep, and has gradually become the gold-standard and preferred therapeutic drug for animal liver fluke disease worldwide. It targets both adult and immature liver flukes, covering the whole parasitic stage of the pathogen, which endows it with incomparable advantages over traditional anthelmintics. Its core strengths are summarized as follows:

Efficiency: A single oral dose of 10–12 mg/kg can achieve a deworming efficacy of over 95%, effectively eliminating internal parasites and reducing livestock mortality and growth retardation caused by fluke infection;

Safety: It exhibits extremely low host toxicity with mild and rare adverse reactions, and is safe for special livestock groups including pregnant animals, lactating individuals and young growing animals, with no obvious teratogenic or developmental toxic effects;

Triclabendazole Safety | Bloomtechz

Triclabendazole Convenience | Bloomtechz

Convenience: The active pharmaceutical ingredient possesses excellent chemical stability under conventional storage and breeding conditions. It can be processed into diverse dosage forms such as tablets, granules and oral suspensions, adapting to different feeding modes and facilitating large-scale administration in modern intensive breeding farms.

Driven by the rapid expansion of global intensive animal husbandry and the increasing prevalence of livestock fluke diseases, the market demand for triclabendazole has maintained steady growth, with annual global market sales exceeding hundreds of millions of US dollars.

2. Breakthrough applications in human medicine

In 1988, British clinicians pioneered the off-label use of triclabendazole for the treatment of two human fascioliasis cases, achieving remarkable curative effects and filling the clinical gap for refractory human liver fluke infection treatment. Subsequent clinical trials and practical verification further expanded its human medical indications, covering paragonimiasis (lung fluke disease) and other zoonotic trematode infections.

Triclabendazole Human Medicine | Bloomtechz

Triclabendazole Cost | Bloomtechz

Notably, triclabendazole shows prominent therapeutic superiority in clinical cases with drug resistance to the first-line drug praziquantel, serving as a critical alternative rescue medication. Recognizing its high efficacy and safety in human parasitic disease treatment, the World Health Organization (WHO) has formally listed triclabendazole as a core recommended drug for Fasciola hepatica infection. It is widely promoted and applied in fluke-endemic regions such as Africa, South America and parts of Asia, becoming an essential pharmaceutical tool for global parasitic disease prevention and control.

Optimization of Synthesis Process: Green Chemistry and Industrial Upgrading

1.Traditional synthetic route
 

The early process used 4-chloro-5- (2,3-dichlorophenoxy) -2-nitroaniline as the raw material, and prepared trichloropyrazole through three steps of trichlorosilane reduction, carbon disulfide cyclization, and dimethyl carbonate methylation, with a total yield of about 55-60%. But this route has the following issues:

 

The use of highly toxic trichlorosilane and carbon disulfide poses a high safety risk;

 

The cyclization step generates hydrogen sulfide gas, which requires a complex tail gas treatment device;

 

The cost of methylation reagent dimethyl carbonate is relatively high.

2.Green synthesis technology innovation
 

Since the 21st century, researchers have developed more environmentally friendly synthesis routes through catalyst design, reaction condition optimization, and other means.

 

Nitro reduction: using iron powder/hydrochloric acid system or catalytic hydrogenation method to reduce the use of trichlorosilane;

 

Ring reaction: replace carbon disulfide with thioacetamide to avoid the formation of hydrogen sulfide;

 

Methylation process: using inexpensive dimethyl sulfate (requiring strict temperature control) or iodomethane (high yield but high cost), some enterprises achieve large-scale production through continuous flow reactors.

 

For example, a patented technology reduces the release rate of hydrogen sulfide in the cyclization reaction by 80% by adjusting the feeding sequence, while increasing the overall yield to 81.5% and achieving a purity of over 99%.

Quality service

Relying on its own synthetic process system, multi-level production facilities, complete quality control system, and global supply chain capabilities, Bloomtechz offers a full-scale, practical, commercializable, and registrable OEM/ODM custom manufacturing system for Triclabendazole Powder. This covers product specification customization, formulation modification manufacturing, branded labeling, graded and packaged production, process scale-up manufacturing, registration document customization, flexible production capacity, global compliant shipping, and commercial technical confidentiality, providing a full set of services. It fully meets the needs of customers in research, clinical, formulation production, brand sales, and cross-border trade scenarios, offering partners a one-stop supply chain solution of "no need to build a factory, no R&D required, full-process management, and launch under your own brand."

Exclusive Brand Visual Customization
Clients can provide their company logo, brand name, product layout, promotional style, and color scheme. Our professional design team will assist for free with label layout, packaging design, manual customization, and certification customization. We can create multiple visual systems according to the client's market positioning, such as high-end research versions, industrial mass-production versions, veterinary medicine versions, and export versions, to meet different sales channel requirements.

Triclabendazole Supplier | Bloomtechz
Triclabendazole Product | Bloomtechz

All finished products' spray codes, batch numbers, production dates, expiration dates, and traceability information are fully customized according to the client's brand system for complete brand privatization.
Differentiated Market Label Adaptation
For different countries and regional market access requirements, we support multi-language label customization.

We can create multi-language packaging and manuals in English, French, Spanish, Arabic, and more, suitable for global cross-border distribution, overseas brand registration, and end-user sales. We also support client-exclusive anti-counterfeit marks, traceable QR codes, and batch traceability codes to help regulate channels, prevent product diversion, and enhance brand credibility and product premium value.
Full-Process Private Label Confidentiality

Triclabendazole Drug | Bloomtechz
Triclabendazole Buy | Bloomtechz

All OEM private label orders are managed with separate files, independent production scheduling, independent packaging, and separate warehousing. Cooperation information is not disclosed externally, client brand plans are not shared, and private label specifications and pricing systems are not revealed to third parties. We can sign exclusive confidentiality agreements to fully protect client brand independence and market exclusivity, preventing homogeneous competition and the risk of business information leaks.

Frequently Asked Questions
 
 

Q1: Will small-batch R&D orders be delayed because of mass production scheduling?

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No. Bloomtechz has dedicated capacity zones for triclabendazole powder, separating the mass production of veterinary raw materials from the small R&D orders, reserving exclusive capacity for samples. Regardless of peak production or sales seasons, gram-level and kilogram-level R&D orders can be scheduled and delivered on time, with the sales team keeping customers updated on production milestones to prevent any order delays.

Q2: Can long-term procurement ensure consistent batch physical and chemical properties?

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Yes. For long-term partners, we standardize the entire production process including synthesis, purification, and drying, strictly controlling moisture content, purity, and particle size stability to avoid batch discrepancies. All batches are retained for records and samples, and we can provide batch consistency documents to support stable formulation adjustment and scale-up applications.

Q3: How to prevent powder from caking and degrading due to moisture during cross-border transport?

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Triclabendazole is prone to moisture and degradation. Bloomtechz uses sealed, moisture-proof double-layer packaging combined with low-temperature, light-avoiding transport to completely block humidity and high temperatures. Special moisture-proof reinforced packaging for cross-border shipping can effectively prevent powder from absorbing moisture and caking, ensuring quality remains stable during long-distance transport.

Q4: During tight supply periods, do you support free production reservation and flexible rescheduling?

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Yes. For customer project adjustments, we can reserve production capacity for free and flexibly postpone delivery without rescheduling penalties. The sales team updates inventory and capacity in real time, forecasts supply fluctuations, and proactively informs customers of delivery risks, fitting their flexible project stocking schedules.

Q5: Can export orders avoid customs classification and compliance risks for this product category?

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Yes. Bloomtechz is well-versed in triclabendazole import/export compliance standards and can provide complete MSDS, COA, and dedicated classification documents that precisely meet customs regulations. This helps minimize inspections and detentions, ensuring smooth customs clearance and stable delivery for clients worldwide.

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