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About This Item
Linear Formula:
HOC6H4CHO
CAS Number:
Molecular Weight:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-599-1
Beilstein/REAXYS Number:
471352
MDL number:
Product Name
4-Hydroxybenzaldehyde, ≥95.0% (HPLC)
InChI key
RGHHSNMVTDWUBI-UHFFFAOYSA-N
InChI
1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H
SMILES string
[H]C(=O)c1ccc(O)cc1
assay
≥95.0% (HPLC)
form
solid
mp
112-116 °C (lit.)
functional group
aldehyde
Quality Level
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Application
4-Hydroxybenzaldehyde may be used as a reactant during the synthesis of 4-(4-hydroxyphenyl)-but-3-ene-2-one (a raspberry ketone precursor) and [(pyrrole-2,5-diyl)-co-(benzylidene)]. It may also be used to prepare nonlinear optical quinolinium single crystals (an OHQ–TMS compound) via a condensation reaction with 1,2-dimethylquinolinium 2,4,6-trimethylbenzenesulfonate in methanol.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
345.2 °F
flash_point_c
174 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Polymerization of pyrrole with 4-hydroxybenzaldehyde over Al-MCM-41 mesoporous aluminosilicate materials.
Chikh K, et al.
Research on Chemical Intermediates, 41(9), 6485-6496 (2015)
Autotoxic antibiotic production by a marine Chromobacterium.
Andersen RJ, et al.
Marine biology, 27(4), 281-285 (1974)
New phenolic N-methylquinolinium single crystals for second-order nonlinear optics.
Kim JS, et al.
Opt. Mater., 45, 136-140 (2015)
Secondary amide-based linkers for solid phase organic synthesis.
Swayze EE.
Tetrahedron Letters, 38(49), 8465-8468 (1997)
Preparation of a raspberry ketone precursor in the presence of rare earth oxide catalysts.
Hoelderich WF and Ritzerfeld V.
Applied Catalysis A: General, 504, 654-663 (2015)
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