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Dokumente

105910

Sigma-Aldrich

Salicylsäure

ReagentPlus®, ≥99%

Synonym(e):

2-Hydroxybenzoesäure

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About This Item

Lineare Formel:
2-(HO)C6H4CO2H
CAS-Nummer:
69-72-7
Molekulargewicht:
138.12
Beilstein:
774890
EG-Nummer:
200-712-3
MDL-Nummer:
MFCD00002439
UNSPSC-Code:
12352100
PubChem Substanz-ID:
57646810
NACRES:
NA.21

Dampfdichte

4.8 (vs air)

Qualitätsniveau

100

Dampfdruck

1 mmHg ( 114 °C)

Produktlinie

ReagentPlus®

Assay

≥99%

bp

211 °C (lit.)
211 °C/20 mmHg

mp (Schmelzpunkt)

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)

InChIKey

YGSDEFSMJLZEOE-UHFFFAOYSA-N

Angaben zum Gen

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

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Allgemeine Beschreibung

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.

Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

314.6 °F - closed cup

Flammpunkt (°C)

157 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
STBL4723
STBL2005
STBK9950
STBK5553
STBK4578

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Salicylsäure European Pharmacopoeia (EP) Reference Standard

S0200000

Salicylsäure

Salicylsäure Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1013

Salicylsäure

Salicylsäure United States Pharmacopeia (USP) Reference Standard

USP

1609002

Salicylsäure

Maltose, Monohydrat suitable for microbiology

Millipore

1.05910

Maltose, Monohydrat

Salicylsäure fine powder EMPROVE® ESSENTIAL Ph Eur,BP,USP

SAFC

1.00635

Salicylsäure

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
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
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
Loretta Lazzarato et al.
Journal of medicinal chemistry, 51(6), 1894-1903 (2008-02-26)
A new class of products in which the phenol group of salicylic acid is linked to alkanoyl moieties bearing nitrooxy functions has been synthesized and studied for their polyvalent actions. The products were stable in acid and neutral media, while
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