Wszystkie zdjęcia(3)
Key Documents
15411
Boc-Cys-OH
for chiral derivatization, LiChropur™, ≥98.5%
Synonim(y):
Boc-L-cysteine
Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych
About This Item
Wzór empiryczny (zapis Hilla):
C8H15NO4S
Numer CAS:
Masa cząsteczkowa:
221.27
Beilstein:
2450705
Numer MDL:
Kod UNSPSC:
41116105
eCl@ss:
32160406
Identyfikator substancji w PubChem:
NACRES:
NA.22
Polecane produkty
klasa czystości
for chiral derivatization
Poziom jakości
linia produktu
ChiraSelect™
Próba
≥98.5%
Postać
solid
aktywność optyczna
[α]20/D +8.0±1.5°, c = 1% in ethanol
czystość optyczna
enantiomeric ratio: ≥99.5:0.5
jakość
LiChropur™
metody
HPLC: suitable
ciąg SMILES
CC(C)(C)OC(=O)N[C@@H](CS)C(O)=O
InChI
1S/C8H15NO4S/c1-8(2,3)13-7(12)9-5(4-14)6(10)11/h5,14H,4H2,1-3H3,(H,9,12)(H,10,11)/t5-/m0/s1
Klucz InChI
ATVFTGTXIUDKIZ-YFKPBYRVSA-N
Opis ogólny
Boc-L-cysteine (Boc-Cys-OH) is a high performance liquid chromatography (HPLC) grade chromatographic solvent.
Zastosowanie
Boc-L-cysteine (Boc-Cys-OH) can may be used as a chromatographic solvent, in an experimental study done to study the biosynthesis of S-(3-hexan-1-ol)-glutathione (3MH-S-glut) and S-(3-hexan-l-ol)-L-cysteine (3MH-S-cys), which act as flavour precursors in wines, in Vitis vinifera grapes exposed to various environmental stress.
Inne uwagi
Chiral derivatizing agent used together with OPA for assaying the enantiomeric purity of amino acids
Informacje prawne
ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.
Kod klasy składowania
13 - Non Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
Eyeshields, Gloves, type N95 (US)
Wybierz jedną z najnowszych wersji:
Masz już ten produkt?
Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Klienci oglądali również te produkty
A Hashimoto et al.
Journal of chromatography, 582(1-2), 41-48 (1992-11-06)
The concurrent determination of free amino acid enantiomers and non-chiral amino acids in rat brain and serum was accomplished by high-performance liquid chromatography with fluorimetric detection after derivatization with N-tert.-butyloxycarbonyl-L-cysteine and o-phthaldialdehyde. The method revealed the presence of a large
Reduction-responsive polymeric micelles for anticancer drug delivery.
Xulin Jiang et al.
Journal of controlled release : official journal of the Controlled Release Society, 152 Suppl 1, e36-e37 (2011-12-27)
Kouji Uda et al.
Amino acids, 48(2), 387-402 (2015-09-10)
Free D-amino acids have been found in various invertebrate phyla, while amino acid racemase genes have been identified in few species. The purpose of this study is to elucidate the distribution, function, and evolution of amino acid racemases in invertebrate
Ryushi Kawakami et al.
Journal of bioscience and bioengineering, 124(1), 23-27 (2017-03-28)
A novel amino acid racemase with broad substrate specificity (BAR) was recently isolated from the hyperthermophilic archaeon Pyrococcus horikoshii OT-3. Characterization of this enzyme has been difficult, however, because the recombinant enzyme is produced mainly as an inclusion body in
Gantumur Battogtokh et al.
Nanomedicine : nanotechnology, biology, and medicine, 18, 315-325 (2018-11-06)
Photodynamic therapy is a clinically approved treatment approach for cancer. However, it has limited applications owing to poor water solubility and the short wavelength absorption of the photosensitizer (PS). We selected a near-infrared photosensitizer, SiNC, and encapsulated into a gold
Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.
Skontaktuj się z zespołem ds. pomocy technicznej