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S7401

Sigma-Aldrich

Salicylic acid

suitable for plant cell culture

Sinônimo(s):

2-Hydroxybenzoic acid

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About This Item

Fórmula linear:
2-(HO)C6H4CO2H
Número CAS:
69-72-7
Peso molecular:
138.12
Beilstein:
774890
Número CE:
200-712-3
Número MDL:
MFCD00002439
Código UNSPSC:
12352207
ID de substância PubChem:
24899745
NACRES:
NA.71

densidade de vapor

4.8 (vs air)

Nível de qualidade

200

pressão de vapor

1 mmHg ( 114 °C)

Ensaio

≥99% (HPLC)

Formulário

powder

técnica(s)

cell culture | plant: suitable

p.e.

211 °C (lit.)

pf

158-161 °C (lit.)

solubilidade

ethanol: 50 mg/mL

densidade

1.44 g/cm3 at 20 °C

cadeia de caracteres SMILES

OC(=O)c1ccccc1O

InChI

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

chave InChI

YGSDEFSMJLZEOE-UHFFFAOYSA-N

Informações sobre genes

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

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Descrição geral

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

Aplicação

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

Ações bioquímicas/fisiológicas

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

Palavra indicadora

Danger

Frases de perigo

H302,H318,H361d

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

314.6 °F - closed cup

Ponto de fulgor (°C)

157 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
SLCF2890
SLCF2889
SLCF2886
SLBZ5366
SLBW0822

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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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