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Merck

S-019

Salicylic acid

1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant®

Synonyme(s) :

2-Hydroxybenzoic acid

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A propos de cet article

Formule linéaire :
2-(HO)C6H4CO2H
Numéro CAS:
69-72-7
Poids moléculaire :
138.12
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329824416
EC Number:
200-835-2
Beilstein/REAXYS Number:
774890
MDL number:
MFCD00002439

Principaux documents

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InChI key

YGSDEFSMJLZEOE-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)c1ccccc1O

grade

certified reference material

vapor density

4.8 (vs air)

vapor pressure

1 mmHg ( 114 °C)

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

1.0 mg/mL in acetonitrile

technique(s)

GC/MS: suitable, gas chromatography (GC): suitable, liquid chromatography (LC): suitable

bp

211 °C (lit.)

Quality Level

300

density

0.782 g/cm3 at 20 °C

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

single component solution

storage temp.

−20°C

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Catégories apparentées

General description

Salicylic acid, the major metabolite of aspirin, is also a phytohormone found in plants with roles in plant growth and development, photosynthesis, transpiration, ion uptake, and transport. This certified solution standard is suitable for numerous LC/MS and GC/MS applications including clinical and diagnostic testing, pharmaceutical research and phytochemical testing.

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Classe de stockage

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

Certificats d'analyse (COA)

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Shifeng Cao et al.
Food chemistry, 134(4), 1715-1718 (2013-02-28)
The effect of elicitors associated with host defence on betacyanin accumulation in Amaranthus mangostanus seedlings was investigated. Under the conditions of the experiments, betacyanin accumulation was generally enhanced by light. Methyl jasmonate (MeJA) treatment increased betacyanin synthesis in a concentration-dependent
A Corina Vlot et al.
Annual review of phytopathology, 47, 177-206 (2009-04-30)
For more than 200 years, the plant hormone salicylic acid (SA) has been studied for its medicinal use in humans. However, its extensive signaling role in plants, particularly in defense against pathogens, has only become evident during the past 20
Ganesan Karthikeyan et al.
British journal of haematology, 146(2), 142-149 (2009-05-15)
Guidelines differ on whether acetyl salicylic acid (ASA, aspirin) should be used for prophylaxis in patients at high-risk of venous thromboembolism (VTE), principally because of differences in perceptions of its efficacy. ASA is an attractive therapeutic option because it is
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
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