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105910

Sigma-Aldrich

Salicylic acid

ReagentPlus®, ≥99%

Sinónimos:

2-Hydroxybenzoic acid

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About This Item

Fórmula lineal:
2-(HO)C6H4CO2H
Número de CAS:
69-72-7
Peso molecular:
138.12
Beilstein/REAXYS Number:
774890
EC Number:
200-712-3
MDL number:
MFCD00002439
UNSPSC Code:
12352100
PubChem Substance ID:
57646810
NACRES:
NA.21

vapor density

4.8 (vs air)

Quality Level

100

vapor pressure

1 mmHg ( 114 °C)

product line

ReagentPlus®

assay

≥99%

bp

211 °C (lit.)
211 °C/20 mmHg

mp

158-161 °C (lit.)

functional group

carboxylic acid

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

signalword

Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

314.6 °F - closed cup

flash_point_c

157 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBL4723
STBL2005
STBK9950
STBK5553
STBK4578

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Salicylic acid European Pharmacopoeia (EP) Reference Standard

S0200000

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Salicylic acid Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1013

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Salicylic acid United States Pharmacopeia (USP) Reference Standard

USP

1609002

Salicylic acid

Maltose monohydrate suitable for microbiology

Millipore

1.05910

Maltose monohydrate

Salicylic acid fine powder EMPROVE® ESSENTIAL Ph Eur,BP,USP

SAFC

1.00635

Salicylic acid

S G Owen et al.
British journal of clinical pharmacology, 38(4), 349-355 (1994-10-01)
1. Five rheumatoid patients with a knee joint effusion participated in the study. An aqueous solution (0.1 to 0.2 ml) containing paracetamol, salicylate, diclofenac and [125I]-albumin was injected into a given joint to yield target concentrations of approximately 20 micrograms
Limor Poraty-Gavra et al.
Plant physiology, 161(3), 1172-1188 (2013-01-16)
How plants coordinate developmental processes and environmental stress responses is a pressing question. Here, we show that Arabidopsis (Arabidopsis thaliana) Rho of Plants6 (AtROP6) integrates developmental and pathogen response signaling. AtROP6 expression is induced by auxin and detected in the
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
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
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
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