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Merck

25102

Sigma-Aldrich

9-Chlormethyl-anthracen

BioReagent, suitable for fluorescence, ≥97.0% (AT)

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About This Item

Empirische Formel (Hill-System):
C15H11Cl
CAS-Nummer:
Molekulargewicht:
226.70
Beilstein:
1873394
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:

Produktlinie

BioReagent

Assay

≥97.0% (AT)

mp (Schmelzpunkt)

138-140 °C (lit.)

Fluoreszenz

λex 356 nm; λem 412 nm (after derivatisation with sodium acetate)

Eignung

suitable for fluorescence

SMILES String

ClCc1c2ccccc2cc3ccccc13

InChI

1S/C15H11Cl/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H,10H2

InChIKey

PCVRSXXPGXRVEZ-UHFFFAOYSA-N

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Hinweis zur Analyse

Zusätzlich zum Emissionsmaximum bei 412 nm sind Nebenpeaks bei 434 nm, 395 nm, 459 nm vorhanden.

Sonstige Hinweise

Blocking group reagent for carboxylic acids, phenols, thiophenols and mercaptans; Derivatizing agent for carboxylic acids giving esters with enhanced UV and fluorescence detection in HPLC

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

W.D. Korte
Journal of Chromatography A, 243, 153-153 (1982)
Jason P Schrum et al.
Journal of the American Chemical Society, 131(40), 14560-14570 (2009-09-18)
The development of a sequence-general nucleic acid copying system is an essential step in the assembly of a synthetic protocell, an autonomously replicating spatially localized chemical system capable of spontaneous Darwinian evolution. Previously described nonenzymatic template-copying experiments have validated the
Dorothea F K Rawn et al.
Journal of chromatography. A, 1080(2), 148-156 (2005-07-13)
A rapid and simple method for confirmation of the diarrhetic shellfish poisons (DSP): okadaic acid (OA), dinophysistoxin-1 (DTX-1) and dinophysistoxin-2 (DTX-2) using fluorescence detection following derivatization with 9-chloromethylanthracene, has been established as an alternate to LC/MS. Exposure of the anthrylmethyl
Zhenming Xie et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 857(1), 53-58 (2007-08-21)
A rapid and sensitive RP-HPLC method with fluorescence detection has been developed for the quantitative analysis of trace amounts of monofluoroacetate (MFA) in biological samples as serum, food and meat. 9-Chloromethylanthracene (9-CMA) is used as the fluorescence labeling reagent. Samples
Ying Zhang et al.
Colloids and surfaces. B, Biointerfaces, 44(2-3), 104-109 (2005-07-26)
Polymeric micelles based on amphiphilic diblock copolymers methoxy poly(ethylene glycol)-polylactide with various hydrophobic lengths were designed as carriers of poorly water-soluble anticancer drug methotrexate (MTX). Relationship between physicochemical characteristics of micelles and release behavior was explored. The critical micelle concentration

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