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Merck

84332

Methyl salicylate

tested according to Ph. Eur.

Synonym(s):

Methylis salicylas, 2-Hydroxybenzoic acid methyl ester, Methyl 2-hydroxybenzoate, Oil of wintergreen, Wintergreen oil

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About This Item

Linear Formula:
2-(HO)C6H4CO2CH3
CAS Number:
119-36-8
Molecular Weight:
152.15
UNSPSC Code:
41116100
NACRES:
NA.21
PubChem Substance ID:
329769295
EC Number:
204-317-7
Beilstein/REAXYS Number:
971516
MDL number:
MFCD00002214

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Product Name

Methyl salicylate, tested according to Ph. Eur.

SMILES string

COC(=O)c1ccccc1O

InChI key

OSWPMRLSEDHDFF-UHFFFAOYSA-N

InChI

1S/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H3

Quality Level

100

agency

tested according to Ph. Eur.

vapor density

5.26 (vs air)

vapor pressure

1 mmHg ( 54 °C)

form

liquid

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.)

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1 of 4

This Item
M6752Y0002083PHL82239
Methyl salicylate tested according to Ph. Eur.

Sigma-Aldrich

84332

Methyl salicylate

Methyl salicylate ReagentPlus®, ≥99% (GC)

Sigma-Aldrich

M6752

Methyl salicylate

Methyl salicylate European Pharmacopoeia (EP) Reference Standard

Y0002083

Methyl salicylate

Methyl salicylate phyproof® Reference Substance

PHL82239

Methyl salicylate

form

liquid

form

liquid

form

-

form

liquid

Quality Level

100

Quality Level

200

Quality Level

-

Quality Level

-

density

1.174 g/mL at 25 °C (lit.)

density

1.174 g/mL at 25 °C (lit.)

density

1.174 g/mL at 25 °C (lit.)

density

1.174 g/mL at 25 °C (lit.)

mp

−8-−7 °C (lit.)

mp

−8-−7 °C (lit.)

mp

−8-−7 °C (lit.)

mp

−8-−7 °C (lit.)

agency

USP/NF

agency

-

agency

-

agency

-

vapor density

5.26 (vs air)

vapor density

5.26 (vs air)

vapor density

5.26 (vs air)

vapor density

5.26 (vs air)

signalword

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN1866
BCCK0726
BCCH5737
BCCG7568
BCCF8811

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Sven Hildebrand et al.
Scientific reports, 9(1), 10880-10880 (2019-07-28)
Optical clearing techniques and light sheet microscopy have transformed fluorescent imaging of rodent brains, and have provided a crucial alternative to traditional confocal or bright field techniques for thin sections. However, clearing and labeling human brain tissue through all cortical
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
Michiel van Wijk et al.
PloS one, 6(7), e21742-e21742 (2011-07-19)
Insect herbivory induces plant odors that attract herbivores' natural enemies. Assuming this attraction emerges from individual compounds, genetic control over odor emission of crops may provide a rationale for manipulating the distribution of predators used for pest control. However, studies
Nadir Erbilgin et al.
Tree physiology, 32(8), 946-957 (2012-06-05)
Coniferous trees have both constitutive and inducible defences that deter or kill herbivores and pathogens. We investigated constitutive and induced monoterpene responses of jack pine (Pinus banksiana Lamb.) to a number of damage types: a fungal associate of the mountain
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
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