3,5-Dimethyl-4-hydroxybenzaldehyde

Names

[ Name ]:
3,5-Dimethyl-4-hydroxybenzaldehyde

[Synonym ]:
Benzaldehyde, 4-hydroxy-3,5-dimethyl-
3,5-Dimethyl-4-hydroxybenzaldehyde
EINECS 218-774-5
4-Hydroxy-3,5-dimethylbenzaldehyde
3,5-dimethyl-4-hydroksybenzaldehyde
MFCD00006946
Benzaldehyde,4-hydroxy-3,5-dimethyl
4-Formyl-2,6-xylenol
4-Hydroxy-3,5-DiMethyl-Benzaldehyde
4-hydroxy-3,5-dimethyl-benzaldehyd
2,6-dimethyl-p-formylphenol

Biological Activity

[Description]:

4-Hydroxy-3,5-dimethylbenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
263.9±35.0 °C at 760 mmHg

[ Melting Point ]:
112-114 °C(lit.)

[ Molecular Formula ]:
C₉H₁₀O₂

[ Molecular Weight ]:
150.17

[ Flash Point ]:
109.7±18.5 °C

[ Exact Mass ]:
150.068085

[ PSA ]:
37.30000

[ LogP ]:
2.31

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.589

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2912499000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2912499000

[ Summary ]:
2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

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)

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

J. Biol. Chem. 262(24) , 11641-6, (1987)

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....

A facile synthesis of 4-alkoxymethylphenols by a copper (II)-acetoxime catalyst/O₂ system. Shimizu M, et al.

Tetrahedron Lett. 32(18) , 2053-2056, (1991)