Methyl salicylate

Modify Date: 2024-01-02 17:01:37

Methyl salicylate Structure
Methyl salicylate structure
Common Name Methyl salicylate
CAS Number 90045-28-6 Molecular Weight 152.14700
Density 1.181 g/mL at 25 °C(lit.) Boiling Point N/A
Molecular Formula C8H8O3 Melting Point N/A
MSDS Chinese USA Flash Point 96℃
Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger

 Names

Name Methyl salicylate

 Chemical & Physical Properties

Density 1.181 g/mL at 25 °C(lit.)
Molecular Formula C8H8O3
Molecular Weight 152.14700
Flash Point 96℃
Exact Mass 152.04700
PSA 46.53000
LogP 1.17880
Storage condition 2-8°C

 Safety Information

Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger
Hazard Statements H302-H315-H318
Precautionary Statements P280-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xn
Risk Phrases 22-36/38
Safety Phrases 26-36
RIDADR NONH for all modes of transport

 Articles5

More Articles
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.

Chem. Res. Toxicol. 23 , 171-83, (2010)

Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental...

Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

J. Med. Chem. 51 , 6740-51, (2008)

The work provides a new model for the prediction of the MAO-A and -B inhibitor activity by the use of combined complex networks and QSAR methodologies. On the basis of the obtained model, we prepared ...

Structure-activity relationship of salicylic acid derivatives on inhibition of TNF-α dependent NFκB activity: Implication on anti-inflammatory effect of N-(5-chlorosalicyloyl)phenethylamine against experimental colitis.

Eur. J. Med. Chem. 48 , 36-44, (2012)

To develop a more potent NFκB inhibitor from salicylic acid which is known to inhibit activity of NFκB, a transcription factor regulating genes involved in immunity, inflammation and tumorigenesis, de...