Skip to Content
Merck
CN

140392

4-Hydroxy-3,5-dimethylbenzaldehyde

95%

Synonym(s):

3,5-Dimethyl-4-hydroxybenzaldehyde

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
HOC6H2(CH3)2CHO
CAS Number:
2233-18-3
Molecular Weight:
150.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848467
EC Number:
218-774-5
Beilstein/REAXYS Number:
1908717
MDL number:
MFCD00006946

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

4-Hydroxy-3,5-dimethylbenzaldehyde, 95%

InChI key

UYGBSRJODQHNLQ-UHFFFAOYSA-N

InChI

1S/C9H10O2/c1-6-3-8(5-10)4-7(2)9(6)11/h3-5,11H,1-2H3

SMILES string

[H]C(=O)c1cc(C)c(O)c(C)c1

assay

95%

mp

112-114 °C (lit.)

functional group

aldehyde

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

4-Hydroxy-3,5-dimethylbenzaldehydewas used as reagent during the phase transfer catalyzed polymerization of 4-hydroxy-3,5-dimethylbenzyl alcohol. It was used as starting reagent during the synthesis of 2,4,6-trimethylphenol.

pictograms

Exclamation mark
GHS07

signalword

Warning

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBB5310V
STBB5310
S65852
S46130
02611JH

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

D J Abraham et al.
Biochemistry, 34(46), 15006-15020 (1995-11-21)
Monoaldehyde allosteric effectors of hemoglobin were designed, using molecular modeling software (GRID), to form a Schiff base adduct with the Val 1 alpha N-terminal nitrogens and interact via a salt bridge with Arg 141 alpha of the opposite subunit. The
A facile synthesis of 4-alkoxymethylphenols by a copper (II)-acetoxime catalyst/O2 system.
Shimizu M, et al.
Tetrahedron Letters, 32(18), 2053-2056 (1991)
P R Ortiz de Montellano et al.
The Journal of biological chemistry, 262(24), 11641-11646 (1987-08-25)
Chloroperoxidase and H2O2 oxidize styrene to styrene oxide and phenylacetaldehyde but not benzaldehyde. The epoxide oxygen is shown by studies with H2(18)O2 to derive quantitatively from the peroxide. The epoxidation of trans-[1-2H]styrene by chloroperoxidase proceeds without detectable loss of stereochemistry
Phase transfer catalyzed polymerization of 4-hydroxy-3, 5-dimethylbenzyl alcohol and copolymerization of 4-bromo-2, 6-dimethylphenol with 4-hydroxy-3, 5-dimethylbenzyl alcohol.
Wang JH and Percec V.
Polym. Bull., 25(1), 25-32 (1991)

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