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140392

4-Hydroxy-3,5-dimethylbenzaldehyde

Name: 4-Hydroxy-3,5-dimethylbenzaldehyde
Brand: ALDRICH

95%

Synonym(s):

3,5-Dimethyl-4-hydroxybenzaldehyde

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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

Assay:

95%

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Properties

Quality Level

100

assay

95%

mp

112-114 °C (lit.)

functional group

aldehyde

SMILES string

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

InChI

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

InChI key

UYGBSRJODQHNLQ-UHFFFAOYSA-N

Description

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

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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How allosteric effectors can bind to the same protein residue and produce opposite shifts in the allosteric equilibrium.

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

Structure-mechanism relationships in hemoproteins. Oxygenations catalyzed by chloroperoxidase and horseradish peroxidase.

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

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)

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Global Trade Item Number

SKU	GTIN
140392-5G	04061831818635