Description
4-{[8-(Acryloyloxy)octyl]oxy}benzoic acid (CAS No. 140918-54-3) is a high-purity, synthetic benzoic acid derivative designed for advanced research and industrial applications. With the molecular formula C18H24O5, this compound features a unique structure combining an acryloyloxy-terminated alkyl chain with a benzoic acid moiety, making it highly versatile for functional material synthesis. It is particularly valuable in polymer chemistry, liquid crystal research, and surface modification studies due to its reactive acrylate group and aromatic carboxylic acid functionality. Our product is rigorously tested for purity and consistency, ensuring optimal performance in sensitive applications. Available in customizable quantities, it is supplied with comprehensive analytical data (including HPLC, NMR, and MS) to meet the stringent requirements of researchers and scientists.
Properties
- CAS Number: 140918-54-3
- Complexity: 358
- IUPAC Name: 4-(8-prop-2-enoyloxyoctoxy)benzoic acid
- InChI: InChI=1S/C18H24O5/c1-2-17(19)23-14-8-6-4-3-5-7-13-22-16-11-9-15(10-12-16)18(20)21/h2,9-12H,1,3-8,13-14H2,(H,20,21)
- InChI Key: NILHWSPFJLBSCB-UHFFFAOYSA-N
- Exact Mass: 320.16237386
- Molecular Formula: C18H24O5
- Molecular Weight: 320.4
- SMILES: C=CC(=O)OCCCCCCCCOC1=CC=C(C=C1)C(=O)O
- Topological: 72.8
- Monoisotopic Mass: 320.16237386
- Synonyms: 140918-54-3, 4-{[8-(Acryloyloxy)octyl]oxy}benzoic acid, 4-[[8-[(1-Oxo-2-propenyl)oxy]octyl]oxy] benzoic acid, 4-(8-prop-2-enoyloxyoctoxy)benzoic acid, 4-((8-(Acryloyloxy)octyl)oxy)benzoic acid, Benzoic acid, 4-[[8-[(1-oxo-2-propen-1-yl)oxy]octyl]oxy]-, 4-(8-acryloyloxyoctyloxy)benzoic acid, 4-[8-acryloyloxyoctyloxy]benzoic acid, MFCD23381869, SCHEMBL1531836, 4-[[8-[(1-Oxo-2-propenyl)oxy]octyl]oxy]benzoic acid, DTXSID50709117, NILHWSPFJLBSCB-UHFFFAOYSA-N, AKOS017342860, 4-[[8-[(1-Oxo-2-propenyl)oxy]octyl]oxy]?benzoic?acid
Application
This compound is widely used as a key intermediate in the synthesis of liquid crystalline polymers and functionalized monomers for advanced materials. Its acrylate group enables photo-polymerization, making it suitable for UV-curable coatings and adhesives. Researchers also utilize it to modify surfaces or create crosslinked networks with tailored mechanical and optical properties.
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