Weight | 150.221 g/mol |
---|---|
Formula | C10H14O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
2-sec-Butylphenol (53466-96-9, 89-72-5)
2-(1-methylpropyl)phenol · ortho-sec-butylphenol
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- Sigma-Aldrich - 2-sec-Butylphenol26.70 USD
- Fisher Scientific - Search for 2-sec-Butylphenol
- TCI - 2-sec-Butylphenol24.00 - 114.00 USD
- Condensations by Sodium. XXXVII. The Dimetalation of Benzene, Thiophene, p-t-Butylphenol, Isopropylbenzene and sec-Butylbenzene and the Effect of Alkoxides on the meta:para Ratio for Benzene1,2 (Journal of the American Chemical Society, 1954)
- Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1. (Biodegradation, 2010)
- A catalytic biofuel production strategy involving separate conversion of hemicellulose and cellulose using 2-sec-butylphenol (SBP) and lignin-derived (LD) alkylphenol solvents. (Bioresource Technology, 2016)
- Degradation of 2-sec-butylphenol: 3-sec-butylcatechol,2-hydroxy-6-oxo-7-methylnona-2,4-dienoic acid, and 2-methylbutyric acid as intermediates (Biodegradation, 1993)
- Liquid-liquid equilibria for 2,3-butanediol + water + 4-(1-methylpropyl)phenol + toluene at 25 C (Journal of Chemical & Engineering Data, 1996)
- Process synthesis and analysis for catalytic conversion of lignocellulosic biomass to fuels: Separate conversion of cellulose and hemicellulose using 2-sec-butylphenol (SBP) solvent (Applied Energy, 2016)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - 2-(1-methylpropyl)phenol
- ortho-sec-butylphenol
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SMILESCCC(C)C1=CC=CC=C1O
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InChIKeyNGFPWHGISWUQOI-UHFFFAOYSA-N
- Pubchem - 2-sec-Butylphenol
- Wikipedia - o-sec-butylphenol
o-sec-Butylphenol is an industrial chemical used in dying and as a chemical intermediate. It is synthesized from phenol and 1-butene in an ortho-alkylation reaction. It is corrosive to the eyes, skin, and gastrointestinal tract.
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Similar Compounds
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