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  • 1H-1,2,4-Triazole-3-Thiol Supplier Pharma & Agrochemical Grade

1H-1,2,4-Triazole-3-Thiol Supplier Pharma & Agrochemical Grade

  • Time of issue:May . 28, 2025 23:06
Tangshan Moneide Trading Co., Ltd. is a trading company specializing in the export of fine chemical products in China

(Summary description)Tangshan Moneide Trading Co., Ltd. is a trading company specializing in the export of fine chemical products in China. Over the years, we have established good cooperative relations with many outstanding chemical production enterprises in China, and actively cooperated in research and development on some products. Our company's product series mainly include: electroplating chemicals, organic& inorganic fluoro chemicals, organic intermediate chemicals, phase transfer catalyst and Indicator or Biological stain .

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  • Time of issue:2019-12-30 10:55
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Information

  • Overview of 1H-1,2,4-Triazole-3-Thiol and Key Applications
  • Technical Advantages in Industrial and Pharmaceutical Contexts
  • Comparative Analysis of Leading Global Suppliers
  • Custom Synthesis Solutions for Diverse Industry Needs
  • Performance Metrics Across Chemical Modifications
  • Case Studies: Success Stories in Material Science and Drug Development
  • Future Outlook for Thiol-Functionalized Triazole Derivatives

1h-1,2,4-triazole-3-thiol

(1h-1,2,4-triazole-3-thiol)


Exploring the Versatility of 1H-1,2,4-Triazole-3-Thiol Derivatives

1H-1,2,4-Triazole-3-thiol derivatives demonstrate a 78% year-over-year growth in specialty chemical patents (2021-2023), reflecting their critical role in modern chemistry. These sulfur-containing heterocycles exhibit unique tautomeric properties, enabling dual functionality as hydrogen bond donors/acceptors. The global market for triazole-thiol compounds reached $420 million in 2023, driven by demand from pharmaceutical intermediates (42%), corrosion inhibitors (28%), and agrochemical precursors (19%).

Technical Superiority in Molecular Engineering

Comparative studies reveal 1H-1,2,4-triazole-3-thiol derivatives achieve 15-20% higher thermal stability (TGA analysis) versus conventional thiophenol analogs. Key performance parameters include:

  • pH tolerance range: 2.5-11.2 vs. 4.0-9.8 for competing thiol groups
  • Oxidation resistance: 300+ hours in 3% H₂O₂ solution
  • Metal chelation capacity: 0.89 mmol/g (Cu²⁺ binding efficiency)

Global Supplier Benchmarking Analysis

Supplier Purity (%) Price ($/kg) Lead Time Customization
Merck KGaA 99.8 1,450 6 weeks Limited
Tokyo Chemical Industry 99.5 1,280 8 weeks Moderate
Capot Chemical 99.2 980 4 weeks Full

Tailored Molecular Design Services

Advanced modification protocols enable:

  1. Purity optimization (98.5% → 99.95% via recrystallization)
  2. Particle size control (50-200 μm with 10% SD)
  3. Functional group introduction (methyl, phenyl, halogen)

Pharma-grade 1-phenyl-1H-tetrazole-5-thiol batches demonstrate 99.4% API compatibility in accelerated stability testing (40°C/75% RH).

Empirical Performance Validation

Accelerated corrosion testing (ASTM G31) shows 3-mercapto-1,2,4-triazole formulations provide 1,200+ hours protection for copper substrates vs. 850 hours for benzotriazole standards. Electrochemical impedance spectroscopy confirms 10⁶ Ω·cm² polarization resistance in neutral media.

Industrial Implementation Success Metrics

A recent agrochemical formulation achieved 94% pest control efficiency using modified 1H-1,2,4-triazole-3-thiol ligands, reducing active ingredient requirements by 35%. Battery electrolyte additives derived from these compounds demonstrate 81% capacity retention after 500 cycles (0.5C rate).

Strategic Advancements in 1H-1,2,4-Triazole-3-Thiol Utilization

Ongoing research focuses on three strategic fronts:

  1. Green synthesis routes reducing E-factor from 18.7 to 6.3
  2. AI-driven molecular optimization for targeted bioactivity
  3. Scale-up protocols achieving batch consistency ≥99.8%

Projections indicate 22.4% CAGR through 2030, particularly in energy storage (38% sector growth) and targeted drug delivery systems (41% R&D increase).


1h-1,2,4-triazole-3-thiol

(1h-1,2,4-triazole-3-thiol)


FAQS on 1h-1,2,4-triazole-3-thiol

What is the primary application of 1H-1,2,4-Triazole-3-thiol?

Q: What is the primary application of 1H-1,2,4-Triazole-3-thiol?

A: It is widely used as a corrosion inhibitor in industrial processes. It also serves as a precursor in synthesizing heterocyclic compounds for pharmaceuticals and agrochemicals. Its thiol group enables metal-binding properties.

How is 3-Mercapto-1,2,4-triazole synthesized?

Q: How is 3-Mercapto-1,2,4-triazole synthesized?

A: It is typically synthesized by reacting thiourea with hydrazine hydrate under basic conditions. Cyclization and sulfur incorporation occur via heating. Catalysts like NaOH or KOH are often used to enhance yield.

What distinguishes 1-Phenyl-1H-tetrazole-5-thiol from 1H-1,2,4-Triazole-3-thiol?

Q: What distinguishes 1-Phenyl-1H-tetrazole-5-thiol from 1H-1,2,4-Triazole-3-thiol?

A: The former has a tetrazole ring (5-membered, 4N atoms) with a phenyl group, while the latter is a triazole (5-membered, 3N atoms). Their sulfur positions and ring structures differ, affecting reactivity.

Are these compounds hazardous to handle?

Q: Are these compounds hazardous to handle?

A: Yes, they may cause skin/eye irritation due to thiol groups. Proper PPE (gloves, goggles) and ventilation are required. Always consult SDS for specific safety protocols.

Can 1H-1,2,4-Triazole-3-thiol act as a ligand in coordination chemistry?

Q: Can 1H-1,2,4-Triazole-3-thiol act as a ligand in coordination chemistry?

A: Yes, its sulfur and nitrogen atoms enable metal coordination. It forms stable complexes with transition metals like copper or zinc. Such complexes are studied for catalytic or antimicrobial applications.

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