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HS Code |
140709 |
| Productname | 2-Methyl-3-Thiosemicarbazide |
| Casnumber | 22314-68-7 |
| Molecularformula | C2H7N3S |
| Molecularweight | 105.17 g/mol |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 123-125°C |
| Solubility | Soluble in water and ethanol |
| Purity | Typically ≥98% |
| Boilingpoint | Decomposes before boiling |
| Storageconditions | Store in a cool, dry place, tightly closed |
| Synonyms | 2-Methylhydrazinecarbothioamide |
| Smiles | CC(NN=C(S)N)=N |
As an accredited 2-Methyl-3-Thiosemicarbazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical 2-Methyl-3-Thiosemicarbazide is packaged in a 25-gram amber glass bottle with a secure screw cap. |
| Shipping | 2-Methyl-3-Thiosemicarbazide is shipped in tightly sealed containers, protected from moisture and light. It is transported according to chemical safety regulations, typically as a non-hazardous substance. The package should be labeled clearly, handled with standard chemical precautions, and stored in a cool, dry place during transit to prevent decomposition. |
| Storage | Store 2-Methyl-3-thiosemicarbazide in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, well-ventilated area, isolated from strong oxidizers and acids. Clearly label the storage area, and restrict access to trained personnel. Follow proper chemical handling protocols and local safety regulations for hazardous substance storage. |
Applications of 2-Methyl-3-Thiosemicarbazide in Industrial ManufacturingAs a primary manufacturer of 2-Methyl-3-Thiosemicarbazide, we supply this specialized intermediate to support production in select chemical sectors where its reactivity and functional group profile directly enhance synthesis efficiency. Deployed within tightly regulated downstream formulations, our material is adopted by leading producers for its track record in precise transformation processes. Below we detail established industrial application scenarios, corresponding compliance frameworks, recommended formulation ratios, key integration steps, and typical finished products. 1. Active Pharmaceutical Ingredient (API) Synthesis – Thiadiazole DerivativesAPI manufacturers employ our material as a nucleophilic agent during condensation routes to construct thiadiazole nuclei, integral to a wide class of anti-inflammatory and cardiovascular therapies. Formulators consistently monitor impurity profiles and reaction yields during the hydrazinolysis and cyclization phases, with in-process controls to meet pharmaceutical quality benchmarks. The input ratio depends on both the desired API target and the stoichiometry required in semi-batch syntheses, balancing purity specifications in finished drug substances supplied to regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate Production – Thiosemicarbazone FungicidesIndustrial formulators in crop protection use this raw material as a core synthon to generate thiosemicarbazone moieties, required for the synthesis of systemic fungicides. The raw material's performance in condensation steps with various aromatic or heterocyclic aldehydes influences downstream efficacy and product shelf life. Dose optimization relates closely to the reactivity of the chosen base stock and the purity mandates for further derivatization, which are stipulated under agricultural substance regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Analytical Reagent Blending – Carbonyl Compound Detection KitsProducers of laboratory diagnostic kits utilize the compound for its selectivity in forming hydrazone derivatives, enabling colorimetric and spectrophotometric detection of trace carbonyls in environmental and industrial samples. The formulation demands precise concentration control to eliminate matrix effects and stabilize working solutions used by accredited laboratories. Final kit assembly involves batch testing and shelf-life verification in compliance with laboratory reagent regulatory frameworks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Dye and Pigment Intermediate Manufacturing – Heterocyclic Scaffold SynthesisColorant manufacturers employ the material within multi-step syntheses to introduce sulfur and nitrogen functionalities into heterocyclic pigment systems. Its intervention in ring-closure reactions plays a determinative role in color intensity and pigment stability over sustained industrial use. Sourcing consistency and additive concentration adjustments depend on end-product chromaticity and performance in targeted applications, such as industrial coatings or specialty inks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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