396206
3,5-Dihydroxybenzyl alcohol
99%
Synonym(s):
5-(Hydroxymethyl)resorcinol
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About This Item
Linear Formula:
(HO)2C6H3CH2OH
CAS Number:
Molecular Weight:
140.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
249-751-8
Beilstein/REAXYS Number:
2326351
MDL number:
Product Name
3,5-Dihydroxybenzyl alcohol, 99%
InChI key
NGYYFWGABVVEPL-UHFFFAOYSA-N
InChI
1S/C7H8O3/c8-4-5-1-6(9)3-7(10)2-5/h1-3,8-10H,4H2
SMILES string
OCc1cc(O)cc(O)c1
assay
99%
form
powder
mp
182-186 °C (dec.) (lit.)
functional group
hydroxyl
Quality Level
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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.
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
A new convergent approach to monodisperse dendritic macromolecules.
Hawker C and Frechet JMJ.
Journal of the Chemical Society. Chemical Communications, 15, 10101-10113 (1990)
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)
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
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