Description

(4-Bromobutoxy)benzene (CAS No. 1200-03-9) is a high-purity organic compound with the molecular formula C₁₀H₁₃BrO. This versatile brominated ether is widely utilized in synthetic organic chemistry, particularly in nucleophilic substitution reactions and as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty materials. The compound features a bromobutyl chain attached to a phenoxy group, offering excellent reactivity for further functionalization. Our product is rigorously tested to ensure ≥98% purity (GC), with stringent quality control to meet the demands of research and industrial applications. Available in quantities ranging from grams to kilograms, (4-Bromobutoxy)benzene is supplied in amber glass bottles or custom packaging to ensure stability and longevity.

Properties

• CAS Number: 1200-03-9
• Complexity: 100
• IUPAC Name: 4-bromobutoxybenzene
• InChI: InChI=1S/C10H13BrO/c11-8-4-5-9-12-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2
• InChI Key: QBLISOIWPZSVIK-UHFFFAOYSA-N
• Exact Mass: 228.01498
• Molecular Formula: C10H13BrO
• Molecular Weight: 229.11
• SMILES: C1=CC=C(C=C1)OCCCCBr
• Topological: 9.2
• Monoisotopic Mass: 228.01498
• Synonyms: (4-Bromobutoxy)benzene, 1200-03-9, 4-Phenoxybutyl bromide, 4-Bromobutyl phenyl ether, Benzene, (4-bromobutoxy)-, 4-bromobutoxybenzene, 1-Bromo-4-phenoxybutane, Phenoxybutyl bromide, Y5HC635AAU, EINECS 214-849-1, NSC-17155, Ether, 4-bromobutyl phenyl, DTXSID90152648, NSC 17155, DTXCID7075139, qblisoiwpzsvik-uhfffaoysa-n, MFCD00000262, Benzene, bromobutoxy-, 4-Phenoxybutylbromide, 4-bromo-1-phenoxybutane, NSC17155, 1-Brom-4-phenoxybutan, 4-phenoxy-butyl bromide, 4-phenoxy-1-bromobutane, 4-phenoxy-1-butylbromide, (4-Bromo-butoxy)-benzene, UNII-Y5HC635AAU, SCHEMBL311427, SCHEMBL27567586, 4-Bromobutyl phenyl ether, 97%, CS-B0148, AKOS000343515, DS-8303, SY010804, NS00023897, P1851, ST51039952, EN300-85792, C11349

Application

(4-Bromobutoxy)benzene is commonly employed as a building block in organic synthesis, particularly in the preparation of phenoxyalkyl derivatives. It serves as a key intermediate in the synthesis of liquid crystals, pharmaceutical agents, and agrochemicals. Researchers also utilize this compound in cross-coupling reactions and as a precursor for functionalized ethers. Its reactive bromobutyl group makes it valuable for introducing phenoxyalkyl moieties into complex molecules.

Safety and Hazards

GHS Hazard Statements

• H302 (16.7%): Harmful if swallowed [Warning Acute toxicity, oral]
• H312 (16.7%): Harmful in contact with skin [Warning Acute toxicity, dermal]
• H315 (83.3%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (83.3%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H332 (16.7%): Harmful if inhaled [Warning Acute toxicity, inhalation]
• H335 (83.3%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (16.7%)
• Acute Tox. 4 (16.7%)
• Skin Irrit. 2 (83.3%)
• Eye Irrit. 2 (83.3%)
• Acute Tox. 4 (16.7%)
• STOT SE 3 (83.3%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.