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Supelco

α-Cyano-4-fluorocinnamic acid

matrix substance for MALDI-MS, ≥95.0% (HPLC)

Synonim(y):

α-Cyano-p-fluorocinnamic acid, 2-Cyano-3-(4-fluorophenyl)-2-propenoic acid, FCCA, NSC 638135

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About This Item

Wzór empiryczny (zapis Hilla):
C10H6FNO2
Numer CAS:
118409-66-8
Masa cząsteczkowa:
191.16
Beilstein:
10339054
Numer MDL:
MFCD00466853
Kod UNSPSC:
12000000
Identyfikator substancji w PubChem:
329767465
NACRES:
NA.21

klasa czystości

matrix substance for MALDI-MS

Poziom jakości

100

Próba

≥95.0% (HPLC)

Postać

crystals

klasy czynnościowe analitów

drugs of abuse, ionic liquids (quantification)

klasy chemiczne analitów

chlorinated lipids, lipids, peptides, phospholipids, phosphopeptides

metody

collision-induced dissociation MS/MS (CID-MS/MS): suitable
matrix-enhanced secondary ion MS (ME-SIMS): suitable

rozpuszczalność

methanol: 100 mg/10 mL, clear, colorless to light yellow

ciąg SMILES

OC(/C(C#N)=C/C1=CC=C(F)C=C1)=O

InChI

1S/C10H6FNO2/c11-9-3-1-7(2-4-9)5-8(6-12)10(13)14/h1-5H,(H,13,14)/b8-5+

Klucz InChI

OBZAFMILNGLRAL-VMPITWQZSA-N

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Zastosowanie

suitable as MALDI-Matrix material

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Piktogramy

Exclamation mark
GHS07

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

H302 + H312 + H332,H315,H319,H335

Klasyfikacja zagrożeń

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organy docelowe

Respiratory system

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
BCBL7696V
BCBL7696

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Dimitrios G Papasotiriou et al.
Journal of proteome research, 9(5), 2619-2629 (2010-04-07)
Peptide Mass Fingerprinting (PMF) of tryptically in-gel digested samples is a well-established protein identification technique for MALDI mass spectrometry but an in-depth PMF evaluation for in-gel digestions of less specific enzymes is still missing. This study demonstrates that the MALDI-LTQ-Orbitrap
Thorsten Jaskolla et al.
Journal of the American Society for Mass Spectrometry, 20(5), 867-874 (2009-02-10)
Phosphatidylethanolamines (PEs) are abundant lipid constituents of the cellular membrane. The amino group of PEs exhibits high reactivity with hypochlorous acid that is generated under inflammatory conditions in vivo. The analysis of the resulting PE mono- and dichloramines is of
Marcel Wiegelmann et al.
Analytical and bioanalytical chemistry, 405(22), 6925-6932 (2012-10-16)
A high analytical sensitivity in ultraviolet matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) is only achieved if the laser wavelength corresponds to a high optical absorption of the matrix. Laser fluence and the physicochemical properties of the compounds, e.g., the
Thorsten W Jaskolla et al.
Journal of proteome research, 8(7), 3588-3597 (2009-05-14)
The performance of the recently developed 4-chloro-alpha-cyanocinnamic acid (Cl-CCA) matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) matrix was investigated in comparison to the most widely used matrix alpha-cyano-4-hydroxycinnamic acid (CHCA). For this purpose, in-solution digestions of standard proteins in
Mark W Towers et al.
Journal of proteome research, 9(4), 1931-1940 (2010-02-13)
Matrix-assisted laser desorption/ionization (MALDI) is a key ionization technique in mass spectrometry (MS) for the analysis of labile macromolecules. An important area of study and improvements in relation to MALDI and its application in high-sensitivity MS is that of matrix
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