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S5922

Sigma-Aldrich

Salicylic acid

BioXtra, ≥99.0%

Synonyme(s) :

2-Hydroxybenzoic acid

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About This Item

Formule linéaire :
2-(HO)C6H4CO2H
Numéro CAS:
69-72-7
Poids moléculaire :
138.12
Numéro Beilstein :
774890
Numéro CE :
200-712-3
Numéro MDL:
MFCD00002439
Code UNSPSC :
12352100
ID de substance PubChem :
24899681
Nomenclature NACRES :
NA.21

Densité de vapeur

4.8 (vs air)

Pression de vapeur

1 mmHg ( 114 °C)

Gamme de produits

BioXtra

Pureté

≥99.0%

Forme

powder or crystals

Technique(s)

tissue culture: suitable (plant)

Impuretés

≤0.015% Phosphorus (P)
≤0.1% Insoluble matter

Résidus de calcination

≤0.01%

Point d'ébullition

211 °C (lit.)

Pf

158-161 °C (lit.)

Solubilité

ethanol: 1 M at 20 °C, clear, colorless

Densité

1.44 g/cm3 at 20 °C

Traces d'anions

chloride (Cl-): ≤0.001%
sulfate (SO42-): ≤0.003%

Traces de cations

Al: ≤0.001%
Ca: ≤0.001%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.01%
Pb: ≤0.001%
Zn: ≤0.0005%

Groupe fonctionnel

carboxylic acid

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

human ... ALB(213) , PTPN1(5770)

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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
GHS08,GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H318,H361d

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

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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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
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
Dorothea Ellinger et al.
Plant physiology, 161(3), 1433-1444 (2013-01-22)
A common response by plants to fungal attack is deposition of callose, a (1,3)-β-glucan polymer, in the form of cell wall thickenings called papillae, at site of wall penetration. While it has been generally believed that the papillae provide a
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
Dmitrij Rekhter et al.
Science (New York, N.Y.), 365(6452), 498-502 (2019-08-03)
The phytohormone salicylic acid (SA) controls biotic and abiotic plant stress responses. Plastid-produced chorismate is a branch-point metabolite for SA biosynthesis. Most pathogen-induced SA derives from isochorismate, which is generated from chorismate by the catalytic activity of ISOCHORISMATE SYNTHASE1. Here
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