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Methyl salicylate

analytical standard

Synonyme(s) :

Essence de gaulthéria, Ester méthylique d’acide 2-hydroxybenzoïque

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About This Item

Formule linéaire :
2-(HO)C6H4CO2CH3
Numéro CAS:
Poids moléculaire :
152.15
Numéro Beilstein :
971516
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Densité de vapeur

5.26 (vs air)

Pression de vapeur

1 mmHg ( 54 °C)

Pureté

≥99.0% (GC)

Température d'inflammation spontanée

847 °F

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.536 (lit.)
n20/D 1.536-1.539

Point d'ébullition

222 °C (lit.)

Pf

−8-−7 °C (lit.)

Densité

1.174 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

COC(=O)c1ccccc1O

InChI

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

Clé InChI

OSWPMRLSEDHDFF-UHFFFAOYSA-N

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Description générale

Methyl Salicylate is a methyl ester of salicylic acid, widely used as phytohormones and defensive signaling compounds. It is most commonly used in topical products as a rubefacients.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Methyl Salicylate may be used as an analytical reference standard for the quantification of the analyte in Ulmus pumila leaves using gas chromatography coupled to mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Health hazardCorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

204.8 °F - closed cup

Point d'éclair (°C)

96 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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Simultaneous determination of salicylic acid, jasmonic acid, methyl salicylate, and methyl jasmonate from Ulmus pumila leaves by GC-MS
Huang H-Z, et al.
International Journal of Analytical Chemistry (2015)
The Essence of Analgesia and Analgesics (2010)
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

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