Chengguan District, Lanzhou, Gansu, China sales01@liwei-chem.com 1557459043@qq.com
Follow us:



Benzyl Butyrate BP EP USP Pharma Grade: Product Commentary

What is Benzyl Butyrate?

Benzyl Butyrate stands out among aromatic esters, well recognized for its presence in pharmaceutical and cosmetic products. The compound shows a clear, slightly oily liquid form at room temperature, giving off a mild, pleasant aroma that hints at fruit and flowers. As a pharma grade ingredient, Benzyl Butyrate produced under BP (British Pharmacopoeia), EP (European Pharmacopoeia), and USP (United States Pharmacopeia) guidelines reflects a higher chemical purity, built for applications demanding strict safety and consistency. Rather than being limited to just one niche, it finds work in a surprising array of formulations from topical creams to oral products, showing flexibility rooted in well-defined chemical properties.

Chemical Structure and Formula

Looking at Benzyl Butyrate at its core, it has the molecular formula C11H14O2 and a molecular weight clocking in at 178.23 g/mol. The molecule forms by linking benzyl alcohol with butyric acid, resulting in an ester bond that sits between the aromatic benzyl group and the straight-chained butyrate. Simple, yes, but that structure makes it both hydrophobic and a good solvent in various chemical systems. It doesn’t solidify under typical storage conditions, holding a density close to 1.01 g/cm3 at 20°C. Unlike powders, flakes, or pearls, the pharma grade variant nearly always appears as a colorless to pale yellow liquid, with no visible contamination or precipitation.

Specifications and HS Code

Chemicals destined for pharmaceutical work carry more demanding requirements than standard industrial supplies. Benzyl Butyrate BP EP USP Pharma Grade is no exception, with published specs laying out limits on identity, assay (purity, not less than 98%), acid value (max 2 mg KOH/g), refractive index (1.498-1.505 at 20° C), and water content (max 0.1%). Regulatory bodies restrict any impurities tightly, especially since trace contaminants can alter therapeutic value or safety profiles. The HS Code for Benzyl Butyrate used in international shipment and customs generally lists under 2916.19, identifying it among other aromatic esters, which assists in compliance with global transport standards.

Properties and Applications

Benzyl Butyrate doesn’t just sit in a vat waiting for someone to notice its smell. It acts as a solvent, flavor ingredient, and carrier for other active molecules, thanks to its chemical stability and miscibility with a range of pharma-grade oils and alcohols. The subtle scent supports perfumes, lotions, and creams. In pharma work, Benzyl Butyrate stands out for its low toxicity profile, low volatility at room temperature, and resistance to hydrolysis under neutral conditions. One measure of its value: it doesn’t just dissolve substances—it helps deliver them in forms that spread easily and keep for long periods. That kind of property cannot be easily swapped for lesser chemicals, especially for people relying on safe, stable medicines.

Safety, Hazard, and Storage

Safety hangs on respect for chemical properties. Benzyl Butyrate, while having a low acute toxicity, earns a “Harmful” warning on some safety labels, largely due to possible irritation if handled with bare skin or splashed in the eyes. In my own workspaces, I’ve seen gloves and goggles treated as more than window dressing, since repeated exposure to strong-smelling esters can trigger allergic reactions or headaches, even if MSDS lists hazards as mild. Its flash point holds at about 127°C, which removes the risk of flame from common heat sources, but calls for clear labeling and storage in cool, ventilated spaces. No one wants chemicals breaking down into something unpredictable, so pharma grade Benzyl Butyrate comes only in tightly sealed, inert containers, usually dark glass or special plastics that keep out air and light.

Raw Materials and Production

Sourcing matters, not just for green claims but because starting with impure benzyl alcohol or butyric acid ruins the finished ester’s pharma grade qualification. Scaled production runs under careful controls, as even small deviations leave behind by-products or unreacted raw material. Waste disposal and worker exposure are also real concerns, stemming from the strong odor and mild corrosiveness of starting acids. Modern factories use closed systems and continuous monitoring, producing a stream of liquid Benzyl Butyrate that needs only simple post-production filtering before being certified. No one walks away from syntheses like this without respect for what tight process control achieves—pharma grade chemicals don’t just “happen,” they’re built up by doing every step right.

Solutions to Industry Challenges

Pharma and cosmetic firms struggle with variable quality and safety concerns for raw materials. Benzyl Butyrate BP EP USP addresses these by providing assurance—independent verification, published specs, and clear traceability through documentation. Manufacturers who cut corners on specs sometimes find hidden costs when regulatory audits show residue or hazardous by-products. Choosing a pharma standard means less re-testing, greater trust from regulatory partners, and more predictable shelf life. In my experience, shifting to certified grades also opened markets abroad, since international buyers treat standardization and traceability as a given, not a luxury. Investments in modern handling—dedicated storage drums, anti-contamination measures, and robust documentation—bring down incident rates and boost returns, even if the road there takes learning new procedures and building new partnerships with suppliers.