Thiabendazole 148-79-8
9 Inquiries
148-79-8
Industrial Grade
99%
sh
orient
1KG, 5KG, 25KG
Yes
2028-05-26
pharmaceutical intermediates,peptides,electronic chemicals
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Product Details
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Seller Information
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Inquiry History
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DescriptionECHEMI Editorial ReferenceThiabendazole, as a member of the benzimidazole class of compounds, is unique in that it carries a 1,3-thiazole-4-yl substituent at position 2. This compound has demonstrated significant fungicidal effects in the agricultural field, particularly in the post-harvest stage, with excellent control over a range of pathogens such as Aspergillus, Botrytis, Cladosporium, and Phytophthora. Thiabendazole typically appears as a white or cream-colored odorless powder that sublimes at temperatures above 590°F and emits a bright light in acidic solutions. Its applications are widespread, and it can be applied in the form of dust, flowing powder, or water-dispersible powder to ensure systemic control of fungi and parasites. The background of the drug's development is also noteworthy. As a 2-substituted benzimidazole drug, it was first introduced in 1962 and quickly became the preferred treatment for a range of nematode infections, particularly in the treatment of strongyluria. However, Thiabendazole is not without side effects, and it may have adverse effects on the central nervous system and potentially exhibit liver toxicity, as detailed in Smith and Leonard's "Pharmacology" (1992 edition, page 919). Despite Thiabendazole's former prominence in the treatment of intestinal threadworms and strong linear worm infections, its status has been challenged in recent years with the emergence of more tolerant drugs. In particular, the potential for liver damage, while rare but potentially serious, has accelerated the development and application of alternative drugs. As for the mechanism of action of Thiabendazole, while it is not yet fully understood, studies have shown that it can inhibit the parasite-specific mitochondrial enzyme succinate dehydrogenase, thereby disrupting the citric acid cycle, mitochondrial respiration, and ATP production, ultimately leading to the death of the parasite. Additionally, Thiabendazole is thought to inhibit microtubule polymerization by binding to β-tubulin, thereby exerting ovicidal effects on certain nematodes. These findings provide valuable insights into the pharmacological action of Thiabendazole.Basic Info
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Product Name:
Thiabendazole
Other Name:1H-Benzimidazole,2-(4-thiazolyl)-;Benzimidazole,2-(4-thiazolyl)-;2-(4-Thiazolyl)-1H-benzimidazole;MK 360;Mintezol;Thiabendazole;Thiabenzole;2-(4-Thiazolyl)benzimidazole;TBZ 60W;Mertect 160;Mertect;TBZ;Thiabendazol;Tecto;Thibenzol;2-(4′-Thiazolyl)benzimidazole;Equizole;Tecto 60;Mintesol;Thibenzole;Thibenzole 200;Tiabendazol;Tiabendazole;Minzolum;Triasox;Omnizole;Tiabenda;Metasol TK 100;Tebuzate;TBZ 6;Tecto 40F;Tecto 10P;Tibimix 20;Thibendole;Thiabendole;Sistesan;Sanaizol 100;MSD 18;Chemviron TK 100;Tecto B;5-(4-Thiazolyl)benzimidazole;G 491;Storite;Ormogal;Cropasal;Mertect 340F;Tectab;Tecta;Pitrizet;Mertect LSP;Hokkustar HP;Hokustar HP;Syntol M 100;Drawipas;TBZ (fungicide);2-(4′-Thiazoyl)benzimidazole;2-(4-Thiazolyl)-1H-benzoimidazole;Amolden HS;2-(4-Triazolyl)benzimidazole;Bovizole;Lombristop;Polival;Top Form Wormer;Thiaben;Eprofil;Nemapan;Sanaizol TBZ-FL 25;NSC 525040;NSC 90507;Marukacide M 101;2-(1,3-Thiazol-4-yl)-1H-benzimidazole;Metasol TK 25AD;TK 25AD;Irgaguard F 3000;Metasol TK 25;4-(1H-Benzimidazol-2-yl)thiazole;Metasol TK 50AD;2-(4-Thiazoyl)benzimidazole;Biogard TBH;2-(1,3-Thiazol-4-yl)benzimidazole;2-(1,3-Thiazol-4-yl)-1H-1,3-benzodiazole;Neo-Sintol AF 75;94977-06-7;98002-42-7;123242-33-1;8018-04-0;8027-10-9;8028-27-1;145316-67-2;1135441-27-8
CAS No.:148-79-8
Molecular Formula:C10H7N3S
InChIKeys:InChIKey=WJCNZQLZVWNLKY-UHFFFAOYSA-N
Molecular Weight:201.25
Exact Mass:201.25
EC Number:205-725-8
UNII:N1Q45E87DT
NSC Number:757347|525040|90507
UN Number:3077|2588
DSSTox ID:DTXSID0021337
NCI Thesaurus Code:C873
Color/Form:Colorless crystals|White crystals|Off-white powder|White to practically white powder|White to tan crystals
ATC Code:D - Dermatologicals|P - Antiparasitic products, insecticides and repellents
HScode:29341000
Categories:
Characteristics-
PSA:
69.8
XLogP3:2.2
Appearance:light yellow powder
Density:1.2271 (rough estimate)
Melting Point:304-305 °C
Boiling Point:446.0±37.0 °C(Predicted)
Flash Point:226.2±16.9 °C
Refractive Index:1.5500 (estimate)
Water Solubility:H2O: 0.005 g/100 mL;soluble in methanol and dimethyl sulfoxide.
Storage Conditions:0-6°C
Vapor Pressure:Negligible at room temperature
Toxicity:Oral-Rat LD50: 2080 mg/kg; Oral-Mouse LD50: 1300 mg/kg
Flammability characteristics:Combustion produces toxic nitrogen oxide and sulfur oxide gas
Odor:Odorless
Taste:Tasteless
PKA:4.64(at 25 °C)
Henrys Law Constant:Henry's Law constant = 2.12X10-11 atm-cu m/mol at 25 °C (est)
Dissociation Constants:4.64 (at 25 °C)|pKa = 4.64
Collision Cross Section:164.17 Ų [M+Na]+ [CCS Type: DT, Method: stepped-field]|144.6 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|137.7 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]|136.19 Ų [M+H]+ [CCS Type: TW]|138.9 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated]|141.7 Ų [M+H]+ [CCS Type: TW, Method: calibrated with Waters Major Mix]|152.4 Ų [M+Na]+ [CCS Type: TW, Method: calibrated with Waters Major Mix]|141.71 Ų [M-H]-|144.1 Ų [M-H]-
Experimental Properties:Nonhygroscopic|Sublimes when heated strongly to 310 °C|Hydroxyl radical reaction rate constant = 6.5X10-11 cu cm/molec-sesc at 25 °C (est)
Air and Water Reactions:Insoluble in water.
Reactive Group:Amines, Phosphines, and Pyridines
Reactivity Profile:THIABENDAZOLE is incompatible with a number of pesticides, including copper-containing fungicides, and with highly alkaline materials. It is a chelating agent, binding many metals including iron, but not calcium (NTP, 1992)
Hazard IdentificationClassification of the substance or mixture
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
GHS label elements, including precautionary statements
Pictogram(s)
Signal word Warning
Hazard statement(s) H410 Very toxic to aquatic life with long lasting effects
Precautionary statement(s) Prevention P273 Avoid release to the environment.
Response P391 Collect spillage.
Storage none
Disposal P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
Other hazards which do not result in classification
no data available
Handling and StoragePrecautions for safe handling
Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Conditions for safe storage, including any incompatibilities
Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.
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Seller Information
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Business Type:
Trader
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Main Products:
pharmaceutical intermediates,peptides,electronic chemicals
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Location:
Room 102, 1st Floor, East Office Building, No. 45 Pengwan Road, Qianwan Bonded Port Area, Qingdao Zone, China (Shandong) Pilot Free Trade Zone
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Payment Terms:
100% TT in advance
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Average lead Time:
10 days
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Total Annual Revenue:
$10 million-$25 million
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Total Employees:
51-100
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Year of Establishment:
2024
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Inquiry History9 Inquiries
Country Product Purchase Quantity Date Posted
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100 KG Aug 28, 2026
Kazakstan
Thiabendazole-D₃
1 KG Apr 27, 2026
United Kingdom
Thiabendazole
25 KG Jan 22, 2025 Post an enquiry for this product
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