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112291

Sigma-Aldrich

Ethyl salicylate

99%

Sinonimo/i:

Ethyl 2-hydroxybenzoate

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About This Item

Formula condensata:
2-(HO)C6H4CO2C2H5
Numero CAS:
118-61-6
Peso molecolare:
166.17
Beilstein:
907659
Numero CE:
204-265-5
Numero MDL:
MFCD00002215
Codice UNSPSC:
12352100
eCl@ss:
39024568
ID PubChem:
24847083
NACRES:
NA.22

Tensione di vapore

0.05 mmHg ( 25 °C)

Livello qualitativo

100

Saggio

99%

Indice di rifrazione

n20/D 1.522 (lit.)

P. eboll.

234 °C (lit.)

Punto di fusione

1 °C (lit.)

Densità

1.131 g/mL at 25 °C (lit.)

Gruppo funzionale

ester

Stringa SMILE

CCOC(=O)c1ccccc1O

InChI

1S/C9H10O3/c1-2-12-9(11)7-5-3-4-6-8(7)10/h3-6,10H,2H2,1H3
GYCKQBWUSACYIF-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Ethyl salicylate was hydrolysed to salicylic acid by the use of an extractive electrospray ionisation (EESI) device.

Applicazioni

Ethyl salicylate is a non-steroidal analgesic, anti-inflammatory and antirrheumatic drug. Its complexation with β-cyclodextrin was studied using reversed-phase liquid chromatography.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

212.0 °F - closed cup

Punto d’infiammabilità (°C)

100 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK6575
STBK3711
STBK0661
STBJ0385
STBH3521

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A J Collins et al.
Annals of the rheumatic diseases, 43(3), 411-415 (1984-06-01)
A topically applied rubifacient delivered by aerosol (Deep-Heat) was studied. After spray application to the forearms of volunteers, without massage, the erythema produced was measured by thermography and correlated with the concentration of 2 salicylate components of the mixture found
Xiao-lan Chen et al.
Guang pu xue yu guang pu fen xi = Guang pu, 24(3), 379-380 (2005-03-12)
Atherton-Todd reaction has been extensively applied to the synthesis of phosphates and phosphoroamidates. Under Atherton-Todd reaction conditions, dialkyl phosphites were probably transformed into diakyl phosphorochloridates. We have tried to use Atherton-Todd reaction to synthesize phosphate of salicylic-acid. But when the
A Lapczynski et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 45 Suppl 1, S397-S401 (2007-11-21)
A toxicological and dermatological review of ethyl salicylate when used as a fragrance ingredient is presented.
Amnon C Sintov et al.
Journal of controlled release : official journal of the Controlled Release Society, 79(1-3), 113-122 (2002-02-21)
The aim of this study was to investigate the percutaneous penetration and dermal metabolism of a new potential anti-acne prodrug--TU-2100 [bis(o-carboxyphenyl ethyl ester)nonanedioate] in guinea pigs. The fluxes of this agent through excised skin after applications of TU-2100 gels at
Mauricio Filippa et al.
Journal of pharmaceutical and biomedical analysis, 48(3), 969-973 (2008-07-25)
The complexation of methyl salicylate (MS) and ethyl salicylate (ES), non-steroidal analgesic, anti-inflammatory and antirrheumatic drugs with beta-cyclodextrin (betaCD) has been studied from thermodynamic and structural points of view. The complexation with betaCD has been investigated using reversed-phase liquid chromatography.
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