Benzenemethanol, 3,4-dimethoxy-

Formula: C₉H₁₂O₃
Molecular weight: 168.1898
IUPAC Standard InChI: InChI=1S/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3
IUPAC Standard InChIKey: OEGPRYNGFWGMMV-UHFFFAOYSA-N
CAS Registry Number: 93-03-8
Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
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Other names: Veratryl alcohol; 3,4-Dimethoxybenzyl alcohol; 3,4-Dimethoxyphenylmethyl alcohol; 3,4-Dimethoxybenzenemethanol; NSC 6317; (3,4-Dimethoxyphenyl)methanol
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Other data available:
- Phase change data
- Mass spectrum (electron ionization)
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IR Spectrum

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Data compiled by: Coblentz Society, Inc.

A digitized version of this spectrum is not currently available.

Owner	COBLENTZ SOCIETY Collection (C) 2018 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved.
Source reference	COBLENTZ NO. 1646
Date	Not specified, most likely prior to 1970
Instrument	Not specified, most likely a prism, grating, or hybrid spectrometer.
Data processing	(NO SPECTRUM, ONLY SCANNED IMAGE IS AVAILABLE)

This IR spectrum is from the Coblentz Society's evaluated infrared reference spectra collection.

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Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Column type	Active phase	I	Reference	Comment
Capillary	OV-1	1456.3	Gautzsch and Zinn, 1996	8. K/min; T_start: 35. C; T_end: 300. C

Column type	Active phase	I	Reference	Comment
Capillary	VF-5MS	1506.2	Tret'yakov, 2007	30. m/0.25 mm/0.25 μm, He; Program: Multi-step temperature program; T(initial)=60C; T(final)=270C

Column type	Active phase	I	Reference	Comment
Capillary	DB-1	1449.	Park, Lee, et al., 2004	60. m/0.32 mm/0.25 μm, He, 35. C @ 4. min, 2. K/min, 230. C @ 25. min
Capillary	DB-1	1450.	Park, Lee, et al., 2004	60. m/0.32 mm/0.25 μm, He, 35. C @ 4. min, 2. K/min, 230. C @ 25. min

Column type	Active phase	I	Reference	Comment
Capillary	DB-Wax Etr	2669.	Ibarz, Ferreira, et al., 2006	60. m/0.25 mm/0.25 μm, He, 40. C @ 5. min, 2. K/min, 230. C @ 100. min

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Gautzsch and Zinn, 1996
Gautzsch, R.; Zinn, P., Use of incremental models to estimate the retention indexes of aromatic compounds, Chromatographia, 1996, 43, 3/4, 163-176, https://doi.org/10.1007/BF02292946 . [all data]

Tret'yakov, 2007
Tret'yakov, K.V., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2007. [all data]

Park, Lee, et al., 2004
Park, B.-S.; Lee, K.-G.; Takeoka, G.R., Comparison of three sample preparation methods on the recovery of volatiles from taheebo (Tabebuia impetiginosa Martius ex DC), Flavour Fragr. J., 2004, 19, 4, 287-292, https://doi.org/10.1002/ffj.1345 . [all data]

Ibarz, Ferreira, et al., 2006
Ibarz, M.J.; Ferreira, V.; Hernández-Orte, P.; Loscos, N.; Cacho, J., Optimization and evaluation of a procedure for the gas chromatographic-mass spectrometric analysis of the aromas generated by fast acid hydrolysis of flavor precursors extracted from grapes, J. Chromatogr. A, 2006, 1116, 1-2, 217-229, https://doi.org/10.1016/j.chroma.2006.03.020 . [all data]

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Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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