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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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1 L

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$177.00

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About This Item

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

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Agency

tested according to Ph. Eur.

Quality Level

100

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.)

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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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)

Signal Word

Danger

Hazard Statements

H302,H317,H318,H361d,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - Skin Sens. 1B

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN1866
BCCK0726
BCCH5737
BCCG7568
BCCF8811

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Hsu Shao Feng et al.
Journal of clinical periodontology, 38(7), 637-643 (2011-04-01)
To evaluate the clinical efficacy of subgingival ultrasonic instrumentation irrigated with essential oils (EOs) of residual periodontal pockets. Sixty-four individuals with chronic periodontitis were invited to participate in this randomized, double-blind, parallel, and placebo-controlled clinical trial. All subjects received non-surgical
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
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
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
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