Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

396206

Sigma-Aldrich

3,5-Dihydroxybenzyl alcohol

99%

Synonym(s):

5-(Hydroxymethyl)resorcinol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(HO)2C6H3CH2OH
CAS Number:
Molecular Weight:
140.14
Beilstein/REAXYS Number:
2326351
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

powder

mp

182-186 °C (dec.) (lit.)

SMILES string

OCc1cc(O)cc(O)c1

InChI

1S/C7H8O3/c8-4-5-1-6(9)3-7(10)2-5/h1-3,8-10H,4H2

InChI key

NGYYFWGABVVEPL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Aggregation behavior of 3,5-dihydroxybenzyl alcohol based dendritic polymers has been investigated by dynamic light scattering and transmission electron microscopy. Preparation of dendritic polyether macromolecules based on 3, 5-dihydroxybenzyl alcohol building block and having carboxylate groups as chain-ends has been described.

Application

3,5-Dihydroxybenzyl alcohol may be used as monomer for the synthesis of a series of monodisperse dendritic polyether macromolecules. It may be employed in the synthesis of dimethylsilyl linked dihydroxybenzyl alcohol based dendrimers.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Dendritic polymers containing a dimethylsilyl linked dihydroxybenzyl alcohol backbone: divergent synthesis, aggregation, functionalization, and an evaluation of their applications in catalysis.
Bourrier O and Kakkar AK.
J. Mater. Sci., 13(6), 1306-1315 (2003)
A new convergent approach to monodisperse dendritic macromolecules.
Hawker C and Frechet JMJ.
Journal of the Chemical Society. Chemical Communications, 15, 10101-10113 (1990)
Carlos Martínez-Aquino et al.
Nanomaterials (Basel, Switzerland), 9(2) (2019-03-01)
Gold nanoparticles functionalized with resorcinol moieties have been prepared and used for detecting formaldehyde both in solution and gas phases. The detection mechanism is based on the color change of the probe upon the aggregation of the nanoparticles induced by
Aggregation of 3, 5-dihydroxybenzyl alcohol based dendrimers and hyperbranched polymers, and encapsulation of DR1 in such dendritic aggregates
Bourrier O, et al.
Inorgorganica Chimica Acta, 357(13), 3836-3846 (2004)
Unimolecular micelles and globular amphiphiles: dendritic macromolecules as novel recyclable solubilization agents.
Hawker CJ, et al.
Journal of the Chemical Society. Perkin Transactions 1, 12, 1287-1297 (1993)

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