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p-t-Butylbenzaldehyde

Names

[ CAS No. ]:
939-97-9

[ Name ]:
p-t-Butylbenzaldehyde

[Synonym ]:
4-tert-Butylbenzaldehyde
p-Tertbutyl Benzaldehyde
Benzaldehyde, 4-(1,1-dimethylethyl)-
4-(2-Methyl-2-propanyl)benzaldehyde
MFCD00035742
Benzaldehyde, p-tert-butyl-
EINECS 213-367-9
tert-butylbenzaldehyde
4-t-Butylbenzaldehyde
4-Tert-Butyl Benzaldehyde
p-t-Butylbenzaldehyde
p-tert-Butylbenzaldehyde
4-(1,1-Dimethylethyl)-benzaldehyde

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
240.8±19.0 °C at 760 mmHg

[ Molecular Formula ]:
C11H14O

[ Molecular Weight ]:
162.228

[ Flash Point ]:
96.9±7.6 °C

[ Exact Mass ]:
162.104462

[ PSA ]:
17.07000

[ LogP ]:
3.33

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.525

MSDS

Safety Information

[ Symbol ]:

GHS07, GHS08, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302-H334-H410

[ Precautionary Statements ]:
P261-P273-P342 + P311-P501

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn:Harmful;N:Dangerousfortheenvironment;

[ Risk Phrases ]:
R22;R43;R50/53

[ Safety Phrases ]:
S36/37-S60-S61

[ RIDADR ]:
UN 3082 9/PG 3

[ WGK Germany ]:
2

[ Packaging Group ]:
III

[ Hazard Class ]:
9

[ HS Code ]:
2912299000

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2912299000

[ Summary ]:
2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.

Bioorg. Med. Chem. 15 , 2006-15, (2007)

Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-q...

Competitive inhibition of mushroom tyrosinase by 4-substituted benzaldehydes.

J. Agric. Food Chem. 49(8) , 4060-3, (2001)

A kinetic study of the inhibition of mushroom tyrosinase by 4-substituted benzaldehydes showed that these compounds behave as classical competitive inhibitors, inhibiting the oxidation of L-3,4-dihydr...

A MALDI-chip integrated system with a monitoring window.

Lab Chip 5(4) , 378-81, (2005)

The integration of a monitoring port along the microfluidic path of a MALDI-chip integrated device is described. Optimization of the microreactor design allows longer reaction and measuring times. The...


More Articles


Related Compounds

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