Identification | More | [Name]
4-N-BUTOXYPHENOL | [CAS]
18979-72-1 | [Synonyms]
3-BUTOXYPHENOL 4-BUTOXYPHENOL 4-BUTYLOXYPHENOL 4-N-BUTOXYPHENOL 4-N-BUTYLOXYPHENOL 4-NORMAL-BUTOXYPHENOL HYDROQUINONE MONOBUTYL ETHER HYDROQUINONE MONO-N-BUTYL ETHER P-BUTOXYPHENOL RESORCINOL MONO-N-BUTYL ETHER butoxyphenol DIBUCAINE(CINCHOCAINE) HYDROCHLORIDE 3-BUTOXYPHENOL 96+% Resorcinol Monobutyl Ether m-Butoxyphenol | [EINECS(EC#)]
204-583-4 | [Molecular Formula]
C10H14O2 | [MDL Number]
MFCD00002336 | [Molecular Weight]
166.22 | [MOL File]
18979-72-1.mol |
Chemical Properties | Back Directory | [Melting point ]
65-66 °C(lit.) | [Boiling point ]
269 °C | [density ]
1,05 g/cm3 | [refractive index ]
1.5230-1.5260 | [storage temp. ]
2-8°C | [form ]
clear liquid | [pka]
9.61±0.10(Predicted) | [color ]
Colorless to Light orange to Yellow | [Water Solubility ]
1.37g/L(30 ºC) | [InChIKey]
VGIJZDWQVCXVNL-UHFFFAOYSA-N | [CAS DataBase Reference]
18979-72-1(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. R37/38:Irritating to respiratory system and skin . R40:Limited evidence of a carcinogenic effect. R41:Risk of serious damage to eyes. R43:May cause sensitization by skin contact. R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
1760 | [WGK Germany ]
3
| [HS Code ]
2909500090 |
Hazard Information | Back Directory | [Uses]
3-Butoxyphenol is an inhibitor of oral bacteria. Antibacterial agent. | [Application]
3-Butoxyphenol is used in organic synthesis. It is used to synthesize 3BOP-daC12 Benzoxazine and 2-butoxy-6-benzyloxybenzaldehyde. | [Synthesis]
1)Stir a solution of 1,5-dihydroxybenzene (5 mmol ) and cerium trifluoromethanesulfonate (0.1 mmol ) in 1-butanol (10 mmol, 5.4 mL) at 130 °C for 5 days in round bottom flask. 2)Quench the mixture with water (20 mL). 3)Extract the reaction mixture three times with dichloromethane (3 x10 mL). 4)Wash the combined organic layers with brine (15 mL). 5)Dry the combined organic layers over MgSO4. 6)Concentrate the combined organic layers. 7)Purify the crude product by column chromatography (Cyclohexane-ethyl acetate 99/1) to obtain 3-butoxyphenol.
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