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25102

Sigma-Aldrich

9-(Chloromethyl)anthracene

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

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About This Item

Fórmula empírica (Notação de Hill):
C15H11Cl
Número CAS:
Peso molecular:
226.70
Beilstein:
1873394
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:

linha de produto

BioReagent

Ensaio

≥97.0% (AT)

pf

138-140 °C (lit.)

fluorescência

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

adequação

suitable for fluorescence

cadeia de caracteres SMILES

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

chave InChI

PCVRSXXPGXRVEZ-UHFFFAOYSA-N

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Nota de análise

In addition to the emission maximum at 412 nm, there are lower maxima at 434, 395 and 459 nm.

Outras notas

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

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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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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