Salicylic Acid 2-O-β-D-Glucoside

• CAT Number: R063376
• CAS Number: 10366-91-3
• Molecular Formula: C13H16O8
• Molecular Weight: 300.26
• Purity: ≥95%
• Synonyms: 2-(β-D-Glucopyranosyloxy)-benzoic Acid; o-(Glucopyranosyloxy)-benzoic Acid; o-(β-D-Glucopyranosyloxy)-benzoic Acid; o-(β-D-Glucosyloxy)-benzoic Acid; 2-O-β-Glucopyranosylsalicylic Acid; Salicylic Acid 2-β-D-Glucoside; Salicylic Acid O-Glucoside
• Storage: -20°C
• IUPAC Name: 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid
• InChI: InChI=1S/C13H16O8/c14-5-8-9(15)10(16)11(17)13(21-8)20-7-4-2-1-3-6(7)12(18)19/h1-4,8-11,13-17H,5H2,(H,18,19)/t8-,9-,10+,11-,13-/m1/s1
• InChIKey: TZPBMNKOLMSJPF-BZNQNGANSA-N
• SMILES: C1=CC=C(C(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O

Salicylic Acid 2-O-β-D-Glucoside(CAT: R063376) is a naturally occurring glucoside of salicylic acid, where a glucose molecule is attached to salicylic acid at the 2-hydroxyl position. It is commonly found in plants and is involved in plant defense mechanisms, particularly in response to pathogen attack. The glucoside form allows salicylic acid to be stored and transported within the plant in an inactive state, which can be hydrolyzed to release free salicylic acid when needed. In research, Salicylic Acid 2-O-β-D-Glucoside is studied for its role in plant immunity and signaling pathways, as well as its potential applications in medicinal and cosmetic products due to the anti-inflammatory properties of salicylic acid.