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27301

Sigma-Aldrich

Salicylic acid

meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (calc. to the dried substance)

Synonyme(s) :

2-Hydroxybenzoic acid

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About This Item

Formule linéaire :
2-(HO)C6H4CO2H
Numéro CAS:
Poids moléculaire :
138.12
Numéro Beilstein :
774890
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Densité de vapeur

4.8 (vs air)

Niveau de qualité

Pression de vapeur

1 mmHg ( 114 °C)

Pureté

99.5-100.5% (calc. to the dried substance)

Qualité

meets analytical specification of Ph. Eur., BP, USP

Impuretés

residual solvents, complies
≤0.001% heavy metals (as Pb)
≤0.2% related subst. (HPLC)

Résidus de calcination

≤0.05% (as SO4)

Perte

≤0.3% loss on drying

Point d'ébullition

211 °C (lit.)

Pf

158-161 °C (lit.)
158-161 °C

Traces d'anions

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤200 mg/kg

Adéquation

complies for appearance of solution
complies for identity

Application(s)

pharmaceutical (small molecule)

Chaîne SMILES 

OC(=O)c1ccccc1O

InChI

1S/C7H6O3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H,(H,9,10)

Clé InChI

YGSDEFSMJLZEOE-UHFFFAOYSA-N

Informations sur le gène

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Catégories apparentées

Application

  • Salinity stress management in agriculture: A study demonstrated the application of salicylic acid in ameliorating salinity stress in barley, revealing its potential to enhance crop resilience to saline environments, thereby contributing to sustainable agricultural practices (Hanif et al., 2024).
  • Enhanced pharmaceutical gel performance: Research on nitrocellulose for prolonged permeation of Levofloxacin HCl-Salicylic Acid In Situ gel emphasized its utility in enhancing drug delivery systems, particularly in treating bacterial infections with improved efficacy (Khaing et al., 2024).
  • Biotechnological production of withanolides: Salicylic acid was applied as an elicitor in the hairy root culture of Withania somnifera, significantly boosting the production of withanolides and phenolic acids, vital for pharmaceutical applications due to their therapeutic properties (Halder and Ghosh, 2024).

Pictogrammes

Health hazardCorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

314.6 °F - closed cup

Point d'éclair (°C)

157 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Les clients ont également consulté

Salicylic acid activates nitric oxide synthesis in Arabidopsis.
Zottini M, et al.
Journal of Experimental Botany, 58(6), 1397-1405 (2007)
Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid1.
Cataldo DA, et al.
Communications in Soil Science and Plant Analysis, 6(1), 71-80 (1975)
S Zaugg et al.
Journal of chromatography. B, Biomedical sciences and applications, 752(1), 17-31 (2001-03-20)
Acetylsalicylic acid (Aspirin) is rapidly metabolized to salicylic acid (salicylate) and other compounds, including gentisic acid and salicyluric acid. Monitoring of salicylate and its metabolites is of toxicological, pharmacological and biomedical interest. Three capillary electrophoresis (CE) methods featuring alkaline aqueous
E Benfeldt et al.
Acta dermato-venereologica, 79(5), 338-342 (1999-09-24)
Our aim was to simultaneously investigate 2 techniques for in vivo sampling of peripheral compartment pharmacokinetics after systemic administration of acetylsalicylic acid. Ten volunteers were given 2 g acetylsalicylic acid orally. Blood samples and dialysates from 4 microdialysis probes inserted
Yunlong Du et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(19), 7946-7951 (2013-04-25)
Removal of cargos from the cell surface via endocytosis is an efficient mechanism to regulate activities of plasma membrane (PM)-resident proteins, such as receptors or transporters. Salicylic acid (SA) is an important plant hormone that is traditionally associated with pathogen

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