Skip to Content
Merck
All Photos(2)

Documents

B3000

Sigma-Aldrich

1,4-Benzenedimethanol

99%

Synonym(s):

p-Phenylene dicarbinol, p-Phenylenedimethanol, p-Xylene-α,α′-diol, p-Xylylene dialcohol, NSC 5097

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C6H4(CH2OH)2
CAS Number:
589-29-7
Molecular Weight:
138.16
Beilstein:
2042077
EC Number:
209-641-2
MDL number:
MFCD00004665
UNSPSC Code:
12352100
PubChem Substance ID:
24891677
NACRES:
NA.22

Assay

99%

form

powder

bp

138-143 °C/1 mmHg (lit.)

mp

114-118 °C (lit.)

SMILES string

OCc1ccc(CO)cc1

InChI

1S/C8H10O2/c9-5-7-1-2-8(6-10)4-3-7/h1-4,9-10H,5-6H2

InChI key

BWVAOONFBYYRHY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1,4-Benzenedimethanol acts as a chain extender to prepare dimethylsiloxane-urea-urethane copolymers.

Application

1,4-Benzenedimethanol can be used to prepare:
  • Poly(6-methyl-ε-caprolactone), which is a key intermediate for the synthesis of polylactide based thermoplastic elastomers.
  • A Highly cross-linked polymer named HCP−BDM (hyper cross-linked polymer-1,4-benzenedimethanol) via Friedel−Crafts alkylation in the presence of Lewis acid.
  • Sulfonated polynuclear aromatic resins.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis of the sulfonated condensed polynuclear aromatic (S-COPNA) resins as strong protonic acids
Tanemura K, et al.
Tetrahedron, 67(6), 1314-1319 (2011)
Polydimethylsiloxane-urea-urethane copolymers with 1, 4-benzenedimethanol as chain extender
Ho T, et al.
Macromolecules, 26, 7029-7036 (1993)
Microporous organic polymers synthesized by self-condensation of aromatic hydroxymethyl monomers
Luo Y, et al.
Polym. Chem., 4(4), 1126-1131 (2013)
Tiejun Ge et al.
Polymers, 11(8) (2019-08-03)
In this experiment, terephthalyl alcohol was used as a modifier to modify phenol under both acidic and alkaline conditions to obtain modified phenols with different molecular structures. Subsequently, the modified phenols reacted with paraformaldehyde in an alkaline environment. After foaming
Polylactide-poly (6-methyl-ε-caprolactone)-polylactide thermoplastic elastomers
Martello MT and Hillmyer M A
Macromolecules, 44(21), 8537-8545 (2011)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service