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S7401

Sigma-Aldrich

Salicylic acid

suitable for plant cell culture

Sinonimo/i:

2-Hydroxybenzoic acid

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About This Item

Formula condensata:
2-(HO)C6H4CO2H
Numero CAS:
69-72-7
Peso molecolare:
138.12
Beilstein:
774890
Numero CE:
200-712-3
Numero MDL:
MFCD00002439
Codice UNSPSC:
12352207
ID PubChem:
24899745
NACRES:
NA.71

Densità del vapore

4.8 (vs air)

Livello qualitativo

200

Tensione di vapore

1 mmHg ( 114 °C)

Saggio

≥99% (HPLC)

Forma fisica

powder

tecniche

cell culture | plant: suitable

P. eboll.

211 °C (lit.)

Punto di fusione

158-161 °C (lit.)

Solubilità

ethanol: 50 mg/mL

Densità

1.44 g/cm3 at 20 °C

Stringa SMILE

OC(=O)c1ccccc1O

InChI

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

Informazioni sul gene

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

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Categorie correlate

Descrizione generale

Salicylic acid (SA) is a phenolic compound produced in plants.

Applicazioni

Salicylic acid has been used:
  • to study its effects on glandular trichomes in Artemisia annua
  • to study its effects on DNA methylation in Taraxacum alatum andTaraxacum hemicyclum
  • to study its effects on parasite epidemics in Lolium arundinaceum

Azioni biochim/fisiol

Salicylic acid (SA) plays a role in endogenous signaling for plant disease resistance. SA is also involved in mediating thermogenesis and symptom development.

Avvertenze

Danger

Indicazioni di pericolo

H302 - H318 - H361d

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

314.6 °F - closed cup

Punto d’infiammabilità (°C)

157 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Supelco

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Salicylic acid

Anders Kjær et al.
AoB PLANTS, 2012, pls018-pls018 (2012-07-27)
Glandular trichomes (GT) of Artemisia annua produce valuable compounds for pharmaceutical and industrial uses, most notably the anti-malarial artemisinin. Our aim was to find out whether the density, number and size of GT can be manipulated to advantage by environmental
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
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