105910
Salicylic acid
ReagentPlus®, ≥99%
Synonym(s):
2-Hydroxybenzoic acid
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About This Item
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vapor density
4.8 (vs air)
Quality Level
vapor pressure
1 mmHg ( 114 °C)
product line
ReagentPlus®
Assay
≥99%
bp
211 °C (lit.)
211 °C/20 mmHg
mp
158-161 °C (lit.)
SMILES string
OC(=O)c1ccccc1O
InChI
1S/C7H6O3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H,(H,9,10)
InChI key
YGSDEFSMJLZEOE-UHFFFAOYSA-N
Gene Information
human ... ALB(213) , PTPN1(5770)
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General description
Salicylic acid is an aromatic phenolic derivative. It can be prepared industrially via the Kolbe-Schmitt reaction. It is used as a chemical intermediate in organic synthesis for the synthesis of various organic compounds.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
314.6 °F - closed cup
Flash Point(C)
157 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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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
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