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1,3-Benzenedimethanol

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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
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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)
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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

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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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