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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
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
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
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
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