Products
High Purity and Consistent Quality: BHT features an industrial-grade purity of ≥99%, ensuring reliable and consistent performance in various applications.
Good Thermal Stability: With a melting point of 69–71°C and a high boiling point of 265°C, it maintains stability under elevated temperatures.
Excellent Solubility in Organic Solvents: It is soluble in ethanol, ether, benzene, and most organic solvents, allowing flexibility in formulation and processing.
Stable Chemical Properties: The compound is chemically stable under normal conditions, supporting safe storage and long-term use.
Product Description of Bylaedydryluene CAS#128-37-0
2,6-Di-tert-butyl-4-methylphenol (BHT) is industrial grade with purity ≥99%. It is a white crystalline powder with a faint characteristic odor. Its melting point is 69–71°C, boiling point 265°C; vapor pressure below 0.1 mmHg at 25°C, relative density 1.048 at 20°C. Insoluble in water, it dissolves easily in ethanol, ether, benzene and most organic solvents. It is chemically stable under normal conditions, but incompatible with strong oxidants and strong acids.
Product Application of Bylaedydryluene CAS#128-37-0
Butylated hydroxytoluene (BHT) is broadly applied in flavors and fragrances, biochemical reagents, chemical raw materials, antioxidants, food and feed additives, feed preservation, aromatic hydrocarbons and bulk pharmaceuticals. As a phenolic antioxidant, it effectively suppresses lipid peroxidation and produces electrophilic quinone methide toxicity via oxidative metabolism. Its metabolite can induce lung injury in mice and may accelerate tumor growth.
Parameters
Safety Information
Delivery Time
Inventory 2-3 working days New manufacturing 7-10 working days
Mode of Transportation
1. By Air, fast but expensive.
2. By Sea, usual and economy.
3. By Train, suit for middle Asia countries.
4. By Express, suit for small package.
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1. Why Supply Chain Transparency Matters in Global Chemical Procurement
Chemical buyers evaluate more than price and delivery time. Clear specifications, matching batch documents, consistent packaging information, and traceable logistics all affect customs clearance, warehouse inspection, and production use.
When selecting a supplier, buyers should review how the company confirms specifications, manages documents, handles changes, and responds to problems. Transparent processes help reduce order risks and improve long-term procurement reliability.
2. Seven Essential Details for a Chemical Product Inquiry
A product name alone is often insufficient for an accurate quotation. Buyers should provide the product name and CAS number, key specifications or purity, final application, required quantity, packaging requirements, destination, and expected delivery time or preferred Incoterms.
If COA, SDS, TDS, special labels, certifications, or registration documents are required, these details should also be included in the initial inquiry. Complete information helps suppliers confirm product, logistics, and documentation conditions more efficiently.
3. What Are the Differences Between COA, SDS, and TDS?
A COA is a batch-specific Certificate of Analysis showing test items, required ranges, and actual results. It is mainly used for quality verification and incoming inspection.
An SDS provides safety, handling, storage, emergency, and transportation information. A TDS describes typical product properties, technical parameters, and application guidance. Buyers should confirm the required document version, language, and applicable standards before placing an order.
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Before shipment, confirm the product identity, physical form, transport classification, and applicable regulations. An SDS is an important reference, but the final shipping arrangement must also meet regulatory and carrier requirements.
Packaging, sealing, moisture protection, palletizing, labels, ports, documents, Incoterms, and transport schedules should be clearly confirmed. Early verification helps prevent delays caused by carrier restrictions or incomplete documentation.
5. How to Evaluate Chemical Product Sample Test Results
Sample evaluation should consider both product compliance and application performance. Laboratory results do not always guarantee the same performance in every formulation or production process.
Before testing, record the sample batch, COA, storage condition, and sampling method. During application tests, keep consistent records of formulation, dosage, process conditions, and results. After approval, reconfirm the formal order specifications, inspection method, packaging, and batch documents.
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