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Merck
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Documentos

68082

Supelco

2,4′-Dibromoacetophenone

for HPLC derivatization, LiChropur, ≥99.0% (HPLC)

Sinônimo(s):

4′-Bromophenacyl bromide

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About This Item

Fórmula linear:
BrC6H4COCH2Br
Número CAS:
Peso molecular:
277.94
Beilstein:
607604
Número CE:
Número MDL:
Código UNSPSC:
12000000
ID de substância PubChem:
NACRES:
NA.22

grau

for HPLC derivatization

Nível de qualidade

Ensaio

≥99.0% (HPLC)

forma

solid

qualidade

LiChropur

técnica(s)

HPLC: suitable

pf

108-110 °C (lit.)
108-112 °C

cadeia de caracteres SMILES

BrCC(=O)c1ccc(Br)cc1

InChI

1S/C8H6Br2O/c9-5-8(11)6-1-3-7(10)4-2-6/h1-4H,5H2

chave InChI

FKJSFKCZZIXQIP-UHFFFAOYSA-N

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Aplicação

Derivatisation reagent for HPLC separation of free fatty acids (FFAs) in human plasma, for liquid chromatography-UV-tandem mass spectrometric analysis of perfluorinated carboxylic acids.

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Informações legais

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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A Mehta et al.
Journal of chromatography. B, Biomedical sciences and applications, 719(1-2), 9-23 (1998-12-30)
We report a rapid and sensitive method for separation and quantitation of free fatty acids (FFAs) in human plasma using high-performance liquid chromatography (HPLC). Two established techniques of lipid extraction were investigated and modified to achieve maximal FFA recovery in
Jinxue Qiu et al.
Journal of chromatography. A, 1235, 132-140 (2012-03-10)
The presence of perfluorocarboxylates (PFCAs) in the environment is of increasing concern due to their possible toxicity to humans and bioaccumulation in organisms. PFCAs are frequently found in river water, sediment and organisms and sometimes even in groundwater. In order
Rodrigo G Stábeli et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 142(3-4), 371-381 (2006-01-31)
MjTX-II, a myotoxic phospholipase A(2) (PLA(2)) homologue from Bothrops moojeni venom, was functionally and structurally characterized. The MjTX-II characterization included: (i) functional characterization (antitumoral, antimicrobial and antiparasitic effects); (ii) effects of structural modifications by 4-bromophenacyl bromide (BPB), cyanogen bromide (CNBr)
Youngjin Park et al.
Archives of insect biochemistry and physiology, 60(3), 105-115 (2005-10-20)
We report on a secretory phospholipase A2 (sPLA2) associated with membrane-enriched fractions prepared from hemocytes of the tobacco hornworms, Manduca sexta. Virtually no PLA2 activity was detected in serum of immunologically naive or bacterially challenged hornworms. PLA2 activity was detected
Daniela P Marchi-Salvador et al.
Biochimica et biophysica acta, 1794(11), 1583-1590 (2009-07-21)
For the first time, the structure of a catalytic inactive phospholipase A(2) homolog (Lys49-PLA(2)s) complexed with p-bromophenacyl bromide (BPB) has been solved by X-ray crystallography. Lys49-PLA(2)s are among the main components of Viperidae snake venoms, causing myonecrosis and other actions

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