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About This Item
Linear Formula:
2-(HO)C6H4CO2CH3
CAS Number:
Molecular Weight:
152.15
EC Number:
204-317-7
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
971516
MDL number:
vapor density
5.26 (vs air)
vapor pressure
1 mmHg ( 54 °C)
assay
98%
autoignition temp.
847 °F
refractive index
n20/D 1.536 (lit.)
bp
222 °C (lit.)
mp
−8-−7 °C (lit.)
density
1.174 g/mL at 25 °C (lit.)
SMILES string
COC(=O)c1ccccc1O
InChI
1S/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H3
InChI key
OSWPMRLSEDHDFF-UHFFFAOYSA-N
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Danger
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - Skin Sens. 1B
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Agata Bartyzel et al.
Analytica chimica acta, 707(1-2), 204-209 (2011-10-27)
N,N'-bis-(α-methylsalicylidene)-2,2-dimethyl-1,3-propanediimine (SBTD) modified silica gel was prepared and used as sorbent for solid phase extraction of Cr(III) ions from aqueous solution. This sorbent showed a high sorption affinity for Cr(III) while recovery of Cr(VI) was very low. The analyte ion
Youli Yao et al.
The Plant cell, 23(10), 3842-3852 (2011-10-27)
We have previously shown that local exposure of plants to stress results in a systemic increase in genome instability. Here, we show that UV-C-irradiated plants produce a volatile signal that triggers an increase in genome instability in neighboring nonirradiated Arabidopsis
Prisca S Pierre et al.
Journal of chemical ecology, 37(4), 368-377 (2011-03-31)
Plants attacked by herbivorous insects emit volatile organic compounds that are used by natural enemies to locate their host or prey. The composition of the blend is often complex and specific. It may vary qualitatively and quantitatively according to plant


