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n-Butyl

Updated: 2026-08-07

Overview

n-Butyl (正丁基) is a monovalent alkyl group derived from butane, consisting of a four-carbon chain. It is a fundamental building block in organic chemistry, often used to modify molecules in pharmaceuticals, agrochemicals, and polymers. The radical form (C₄H₉·) is highly reactive, while its derivatives (e.g., n-butyl alcohol, n-butyl lithium) are stable and widely applied. In industrial contexts, n-butyl groups are introduced via alkylation reactions to enhance solubility, volatility, or other physicochemical properties of target compounds. Its versatility makes it indispensable in fine chemical synthesis and bulk manufacturing.

Physical and Chemical Properties

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n-Butyl derivatives exhibit varying physical states depending on functional groups. For example, n-butanol is a colorless liquid, while n-butyl lithium is a pyrophoric solution. The parent hydrocarbon, butane, is a gas under standard conditions. Key properties include low water solubility and high flammability, with flash points often below room temperature for volatile derivatives. Chemically, n-butyl groups participate in nucleophilic substitutions, eliminations, and radical reactions. Their reactivity is leveraged in Grignard reagents and polymerization initiators. Stability varies: n-butyl ethers are relatively inert, whereas n-butyl halides are reactive intermediates.

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Main Applications

The primary use of n-butyl groups is in synthesizing plasticizers like dibutyl phthalate (DBP), which soften PVC products. They also feature in pharmaceuticals, e.g., as lipophilic modifiers in drug molecules to improve bioavailability. In agrochemicals, n-butyl chains enhance pesticide adhesion and penetration. Additionally, n-butyl lithium serves as a strong base in organic synthesis, and n-butyl acetate is a common solvent in coatings and adhesives. Fuel additives like MTBE (methyl tert-butyl ether) historically relied on butyl derivatives for octane improvement.

Safety and Storage

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n-Butyl compounds require strict safety measures due to flammability and reactivity. Store in sealed containers under inert gas (e.g., nitrogen) for air-sensitive derivatives like n-butyl lithium. Avoid contact with oxidizers and ensure ventilation to prevent explosive vapor accumulation. Personal protective equipment (PPE) such as gloves and goggles is mandatory. Spills should be neutralized with appropriate agents (e.g., sand for liquids, alcohol-resistant foam for fires). Always refer to SDS (Safety Data Sheets) for compound-specific protocols.

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B2B Procurement Guide

When procuring n-butyl derivatives, prioritize suppliers with ISO 9001 certification to ensure quality consistency. Specify parameters like purity (e.g., ≥99% for synthesis), moisture content, and impurity profiles. Bulk shipments may require UN-certified packaging for hazardous materials. Negotiate contracts with incoterms clarifying transport responsibilities (e.g., CFR or CIF for international orders). Audit suppliers for compliance with REACH or TSCA regulations. Spot-check batches via third-party labs if used in critical applications like pharmaceuticals.

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