118-61-6 | Ethyl salicylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$13.00	$9.00
1g	95%	in stock	$15.00	$10.00
5g	95%	in stock	$16.00	$11.00
25g	95%	in stock	$19.00	$13.00
100g	95%	in stock	$22.00	$16.00
500g	95%	in stock	$79.00	$55.00
5kg	95%	in stock	$459.00	$321.00
10kg	95%	in stock	$707.00	$495.00
25kg	95%	in stock	$1,525.00	$1,067.00
50kg	95%	in stock	$2,854.00	$1,998.00
200kg	95%	in stock	$7,175.00	$5,023.00

Description

• Catalog Number: AB44113
• Chemical Name: Ethyl salicylate
• CAS Number: 118-61-6
• Molecular Formula: C9H10O3
• Molecular Weight: 166.1739
• MDL Number: MFCD00002215
• SMILES: CCOC(=O)c1ccccc1O
• NSC Number: 8209

Computed Properties

• Complexity: 156
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 3

Upstream Synthesis Route

As a professional chemist, here is a product description focused on the application of Ethyl salicylate in chemical synthesis:Ethyl salicylate, also known as ethyl 2-hydroxybenzoate, is a versatile compound widely utilized in chemical synthesis processes. This organic ester is valued for its pleasant aromatic scent, reminiscent of wintergreen, making it a popular choice in the perfume and fragrance industry. Beyond its olfactory qualities, Ethyl salicylate serves a crucial role as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, Ethyl salicylate acts as a precursor in the preparation of salicylic acid derivatives, which have diverse applications ranging from medicinal compounds to dyes and polymers. Its functional groups enable selective modifications through esterification, hydrolysis, and substitution reactions, allowing chemists to tailor its properties for specific uses. Moreover, Ethyl salicylate's aromatic nature imparts unique characteristics to the synthesized products, enhancing their overall quality and utility.Overall, Ethyl salicylate's versatility and reactivity make it a valuable component in the toolkit of synthetic chemists, enabling the efficient production of a wide range of compounds with tailored properties and applications.

Literature

• Inverse antagonist activities of parabens on human oestrogen-related receptor γ (ERRγ): in vitro and in silico studies.

  Toxicology and applied pharmacology 20130701

• The estrogenic potential of salicylate esters and their possible risks in foods and cosmetics.

  Toxicology letters 20120307

• Optimization and validation of liquid chromatography and headspace-gas chromatography based methods for the quantitative determination of capsaicinoids, salicylic acid, glycol monosalicylate, methyl salicylate, ethyl salicylate, camphor and l-menthol in a topical formulation.

  Journal of pharmaceutical and biomedical analysis 20120223

• On-line reaction monitoring by extractive electrospray ionisation.

  Rapid communications in mass spectrometry : RCM 20110530

• Natural variation in herbivore-induced volatiles in Arabidopsis thaliana.

  Journal of experimental botany 20100601

• The herbivore-induced plant volatile methyl salicylate negatively affects attraction of the parasitoid Diadegma semiclausum.

  Journal of chemical ecology 20100501

• Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: an enzyme directed prodrug approach.

  Chemico-biological interactions 20100212

• Levels of mint and wintergreen flavorants: smokeless tobacco products vs. confectionery products.

  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20100201

• Anti-aphrodisiac compounds of male butterflies increase the risk of egg parasitoid attack by inducing plant synomone production.

  Journal of chemical ecology 20091101

• Synthesis, characterization and texture observations of calamitic liquid crystalline compounds.

  International journal of molecular sciences 20091101

• Flavour compounds in tomato fruits: identification of loci and potential pathways affecting volatile composition.

  Journal of experimental botany 20090101

• Physicochemical interactions between drugs and superdisintegrants.

  The Journal of pharmacy and pharmacology 20081201

• Encapsulation of methyl and ethyl salicylates by beta-cyclodextrin HPLC, UV-vis and molecular modeling studies.

  Journal of pharmaceutical and biomedical analysis 20081104

• Orosensory-directed identification of astringent mouthfeel and bitter-tasting compounds in red wine.

  Journal of agricultural and food chemistry 20080227

• DFT and ab initio study of structure of dyes derived from 2-hydroxy and 2,4-dihydroxy benzoic acids.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080201

• N'-Ferrocenyl-2-hydroxy-benzohydrazide.

  Acta crystallographica. Section E, Structure reports online 20080101

• 4-pyridyl carbonyl and related compounds as thrips lures: effectiveness for onion thrips and new zealand flower thrips in field experiments.

  Journal of agricultural and food chemistry 20070725

• Fragrance material review on ethyl salicylate.

  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20070101

• A rapid HPLC/ESI-MS method for the quantitative determination of oridonin in rat plasma.

  Die Pharmazie 20060901

• [Study on the phosphorylaions reaction between ethyl salicylate and DEPH].

  Guang pu xue yu guang pu fen xi = Guang pu 20040301

• Percutaneous penetration and skin metabolism of ethylsalicylate-containing agent, TU-2100: in-vitro and in-vivo evaluation in guinea pigs.

  Journal of controlled release : official journal of the Controlled Release Society 20020219