Description
4-Pentylbenzoyl chloride (CAS 49763-65-7) is a high-purity organic compound with the molecular formula C12H15ClO. This specialized reagent is widely utilized in synthetic organic chemistry, particularly as an acylating agent for the introduction of the 4-pentylbenzoyl moiety into target molecules. The compound features a reactive benzoyl chloride group adjacent to a pentyl substituent, making it valuable for the synthesis of liquid crystals, pharmaceutical intermediates, and advanced materials. Our product is rigorously tested to ensure superior quality, with typical purity levels exceeding 97% (GC). Supplied in moisture-resistant packaging under inert atmosphere to maintain stability, this chemical is ideal for research and industrial applications requiring precise acylation reactions. Available in quantities ranging from 1g to 1kg to suit various experimental scales.
Properties
- CAS Number: 49763-65-7
- Complexity: 171
- IUPAC Name: 4-pentylbenzoyl chloride
- InChI: InChI=1S/C12H15ClO/c1-2-3-4-5-10-6-8-11(9-7-10)12(13)14/h6-9H,2-5H2,1H3
- InChI Key: FBBRKYLXMNQFQU-UHFFFAOYSA-N
- Exact Mass: 210.0811428
- Molecular Formula: C12H15ClO
- Molecular Weight: 210.70
- SMILES: CCCCCC1=CC=C(C=C1)C(=O)Cl
- Topological: 17.1
- Monoisotopic Mass: 210.0811428
- Synonyms: 4-Pentylbenzoyl chloride, Benzoyl chloride, 4-pentyl-, p-Pentylbenzoyl chloride, 4-n-Amylbenzoyl chloride, EINECS 256-478-8, p-(n-Amyl)benzoyl chloride, DTXSID5068520, DTXCID7040736, 256-478-8, fbbrkylxmnqfqu-uhfffaoysa-n, 49763-65-7, 4-n-Pentylbenzoyl chloride, 4-PentYl-Benzoyl Chloride, 4-PENTYLBENZOYLCHLORIDE, MFCD00000700, 4-(n-pentyl)benzoyl chloride, SCHEMBL158152, 4-pentylbenzoyl chloride (en), 4-(n-pentyl)-benzoyl chloride, p-n-pentylbenzoic acid chloride, 4-Pentylbenzoyl chloride, 96%, 4K9R3634UY, STR01793, 4-(n-pentyl) benzoic acid chloride, SBB057134, AKOS002685613, DB-051689, NS00031964, ST50997489, G77198
Application
4-Pentylbenzoyl chloride serves as a key intermediate in the synthesis of liquid crystal compounds for display technologies. It is employed in pharmaceutical research for the preparation of bioactive molecules through acylation reactions. The compound also finds use in materials science for modifying polymer properties and creating specialized coatings.
Safety and Hazards
GHS Hazard Statements
- H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
- H318 (88.6%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
Precautionary Statements
- P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P405, and P501
Hazard Classes and Categories
- Skin Corr. 1B (100%)
- Eye Dam. 1 (88.6%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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