Description

p-(Hexyloxy)benzaldehyde (CAS: 5736-94-7) is a high-purity organic compound with the molecular formula C₁₃H₁₈O₂. This aromatic aldehyde features a hexyloxy group para-substituted on the benzaldehyde ring, making it a valuable intermediate in fine chemical synthesis. With a purity of ≥98%, it is ideal for research and industrial applications requiring precise reactivity. The compound is characterized by its clear to pale yellow appearance and is supplied in tightly sealed containers to ensure stability. Suitable for use in liquid crystal displays (LCDs), pharmaceuticals, and agrochemicals, this reagent is a must-have for laboratories focused on advanced organic synthesis.

Properties

• CAS Number: 5736-94-7
• Complexity: 160
• IUPAC Name: 4-hexoxybenzaldehyde
• InChI: InChI=1S/C13H18O2/c1-2-3-4-5-10-15-13-8-6-12(11-14)7-9-13/h6-9,11H,2-5,10H2,1H3
• InChI Key: GWXUVWKBVROFDM-UHFFFAOYSA-N
• Exact Mass: 206.130679813
• Molecular Formula: C13H18O2
• Molecular Weight: 206.28
• SMILES: CCCCCCOC1=CC=C(C=C1)C=O
• Topological: 26.3
• Monoisotopic Mass: 206.130679813
• Synonyms: 4-(Hexyloxy)benzaldehyde, 5736-94-7, 4-Hexoxybenzaldehyde, Benzaldehyde, 4-(hexyloxy)-, Benzaldehyde, p-(hexyloxy)-, p-(Hexyloxy)benzaldehyde, ZU34J4QL75, EINECS 227-251-0, NSC 508752, NSC-508752, DTXSID0063995, 4-(N-HEXYLOXY)BENZALDEHYDE, DTXCID4042208, 227-251-0, 4-Hexyloxybenzaldehyde, 4-n-Hexyloxybenzaldehyde, p-Hexyloxybenzaldehyde, p-n-Hexyloxybenzaldehyde, MFCD00016615, p-Hexoxybenzaldehyde, NSC508752, 4-n-hexoxybenzaldehyde, 4-hexyloxy benzaldehyde, 4-hexyloxy-benzaldehyde, UNII-ZU34J4QL75, SCHEMBL895947, SCHEMBL2120140, 4-(Hexyloxy)benzaldehyde, 98%, ALBB-001163, BCP34223, BBL036965, SBB008001, STK500987, AKOS000119908, FH61823, NCGC00340474-01, AS-58236, SY048484, DB-053041, CS-0186888, H0166, NS00033703, ST50307392, EN300-16977, D90810, p-Hexyloxybenzaldehyde;4-N-Hexyloxybenzaldehyde, AB01333447-02, Z56851159

p-(Hexyloxy)benzaldehyde is widely used as a key intermediate in the synthesis of liquid crystal materials for display technologies. It serves as a precursor in the production of pharmaceuticals, particularly in the development of novel therapeutic agents. Additionally, this compound is utilized in agrochemical research for creating specialized pesticides and herbicides. Its reactivity makes it valuable in organic synthesis for constructing complex aromatic aldehydes. Researchers also employ it in material science for developing advanced polymers and coatings.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2A (100%)
• STOT SE 3 (100%)

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