1,3-Benzenedimethanol
1,3-Benzenedimethanol Basic information
- Product Name:
- 1,3-Benzenedimethanol
- Synonyms:
-
- m-Xylene glycol
- 1,3-Phenylenebismethanol
- Isophthalyl alcohol
- 1,3-Bis(hydroxymethyl)benzene~m-Xylene-alpha,alpha-diol
- 1,3-BENZENEDIMETHANOL 98%
- 1,3-Benzenedimethanol,98%
- m-xylene-à,à'-diol
- m-xylene-α,α'-diol
- CAS:
- 626-18-6
- MF:
- C8H10O2
- MW:
- 138.16
- EINECS:
- 210-934-2
- Product Categories:
-
- Benzhydrols, Benzyl & Special Alcohols
- Benzene derivates
- Mol File:
- 626-18-6.mol
1,3-Benzenedimethanol Chemical Properties
- Melting point:
- 56-60 °C (lit.)
- Boiling point:
- 154-159 °C/13 mmHg (lit.)
- Density
- 1.1610
- refractive index
- 1.5090 (estimate)
- Flash point:
- 154-159°C/13mm
- storage temp.
- Sealed in dry,Room Temperature
- form
- Solution, may develop some turbidity precipitate
- pka
- 13.98±0.10(Predicted)
- color
- Clear to hazy colorless to yellow
- Water Solubility
- Soluble in water.
- BRN
- 1562398
- CAS DataBase Reference
- 626-18-6(CAS DataBase Reference)
- EPA Substance Registry System
- 1,3-Benzenedimethanol (626-18-6)
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 20/22-36-22
- Safety Statements
- 9-7-23-26
- WGK Germany
- 3
- TSCA
- Yes
- HS Code
- 29062900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1,3-Benzenedimethanol Usage And Synthesis
Chemical Properties
WHITE CRYSTALLINE POWDER AND CHUNKS
Uses
1,3-Benzenedimethanol was used in the synthesis of a series of cross-linked poly(orthocarbonate)s. It was also used in the synthesis of mixed-tethered system, required for the preparation of e-edge-[60]fullerenylmethanodihydropyrrole adduct.
Synthesis
626-19-7
626-18-6
The general procedure for the synthesis of 1,3-benzenedimethanol from isophthalaldehyde was as follows: in a 25 mL round bottom flask equipped with a magnetic stirrer, an ethanol solution (5 mL) of isophthalaldehyde (1 mmol) was added. Subsequently, P(BVP)BH4 (100 mg) was added to the reaction system and the reaction was stirred at room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was filtered and washed sequentially with 1.0 M hydrochloric acid (2 × 10 mL) and ethanol (25 mL) to remove unreacted reagents. The filtrates were combined and concentrated under reduced pressure to give pure 1,3-benzenedimethanol in moderate to very high yields. For the few cases where the reaction is incomplete, the crude product needs to be purified by silica gel column chromatography using an appropriate eluent (see Scheme 1).
References
[1] Chemistry - A European Journal, 2013, vol. 19, # 24, p. 7701 - 7707
[2] Journal of Organic Chemistry, 2018, vol. 83, # 4, p. 2274 - 2281
[3] Comptes Rendus Chimie, 2013, vol. 16, # 8, p. 721 - 727
[4] Comptes Rendus Chimie, 2014, vol. 17, # 1, p. 23 - 29
[5] Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry, 2003, vol. 42, # 4, p. 744 - 750
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1,3-Benzenedimethanol(626-18-6)Related Product Information
- 2-Methyl-2,4-pentanediol
- Benzyl alcohol
- Ethylene glycol
- Xylene
- Triphenylmethanol
- 4-Hydroxybenzyl alcohol
- Musk xylene
- m-Anisyl alcohol
- Diethylstilbestrol
- Benzhydrol
- Ethylene glycol diacetate
- Diethylene glycol
- Benzene
- PROPYLENE GLYCOL
- 1,2-BENZENEDIMETHANOL,O-BENZENEDIMETHANOL,1,2-BENZENEDIMETHANOL 97%,1,2-Benzenedimethanol,97%
- 1,2,4-Benzenetricarboxylic acid
- 1,2,3-Benzenetricarboxylic acid hydrate
- Trimesic acid