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2,5-Dimethylbenzyl alcohol, 97+%
CAS: 53957-33-8 | C9H12O | 136.194 g/mol
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Catalog number L01624.06
also known as L01624-06
Price (USD)
127.65
Special offer
Online exclusive
Ends: 30-Jun-2026
150.00Save 22.35 (15%)
Each
Quantity:
5 g
Price (USD)
127.65
Special offer
Online exclusive
Ends: 30-Jun-2026
150.00Save 22.35 (15%)
Each
Chemical Identifiers
CAS53957-33-8
IUPAC Name(2,5-dimethylphenyl)methanol
Molecular FormulaC9H12O
InChI KeyLEBQTCCCNMTXSF-UHFFFAOYSA-N
SMILESCC1=CC=C(C)C(CO)=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
Assay (GC)≥97.0%
FormLiquid
Refractive Index1.5335-1.5385 @ 20?C
2,5-Dimethylbenzyl alcohol, is used as a self-indicating standard for the determination of organ lithium reagents
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,5-Dimethylbenzyl alcohol, is used as a self-indicating standard for the determination of organ lithium reagents
Solubility
Difficult in mix.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
2,5-Dimethylbenzyl alcohol, is used as a self-indicating standard for the determination of organ lithium reagents
Solubility
Difficult in mix.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
General References:
- Ching-Yuan Liu.; Paul Knochel. Preparation of Polyfunctional Aryl Azides from Aryl Triazenes. A New Synthesis of Ellipticine, 9-Methoxyellipticine, Isoellipticine, and 7-Carbethoxyisoellipticine. J. Org. Chem. 1992, 72, (19), 7106-7115.
- Gerald Vander Stouw.; Allen R. Kraska.; Harold Shechter. Rearrangement and insertion reactions of 2-methylbenzylidenes. J. Am. Chem. Soc. 1972, 94, (5), 1655-1661.