G5630
Gly-Gly-Gly-Gly-Gly-Gly
solid
Sinonimo/i:
Hexaglycine
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100 MG
104,00 €
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100 MG
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About This Item
Formula empirica (notazione di Hill):
C12H20N6O7
Numero CAS:
Peso molecolare:
360.32
Numero MDL:
Codice UNSPSC:
12352202
ID PubChem:
NACRES:
NA.26
Prodotti consigliati
Nome del prodotto
Gly-Gly-Gly-Gly-Gly-Gly,
Stato
solid
Livello qualitativo
Colore
white
Punto di fusione
314.5 °C
applicazioni
peptide synthesis
Temperatura di conservazione
−20°C
Stringa SMILE
NCC(=O)NCC(=O)NCC(=O)NCC(=O)NCC(=O)NCC(O)=O
InChI
1S/C12H20N6O7/c13-1-7(19)14-2-8(20)15-3-9(21)16-4-10(22)17-5-11(23)18-6-12(24)25/h1-6,13H2,(H,14,19)(H,15,20)(H,16,21)(H,17,22)(H,18,23)(H,24,25)
XJFPXLWGZWAWRQ-UHFFFAOYSA-N
Categorie correlate
Applicazioni
Hexaglycine and capped hexaglycine are used in physicochemical studies of peptide structure dynamics. Hexaglycine is used as a model compound in development of peptide quantitation and separation methods.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
Voislav Blagojevic et al.
The Analyst, 135(6), 1456-1460 (2010-05-26)
A novel method is presented for the quantitation of peptides based on their methylation by in vacuo chemical reaction with methyl iodide. Samples of two small peptides, hexaglycine and pentaalanine, were labeled with CH(3)I and CD(3)I, representing the "unknown" and
Punam Dalai et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 47(4), 427-452 (2016-10-21)
On the Hadean-Early Archean Earth, the first islands must have provided hot and dry environments for abiotically formed organic molecules. The heat sources, mainly volcanism and meteorite impacts, were also available on Mars during the Noachian period. In recent work
Joshua A Plumley et al.
The journal of physical chemistry. B, 115(6), 1562-1570 (2011-01-26)
We compare the energies and enthalpies of inter-action of three- and seven-stranded capped polyglycine aggregates in both the pleated and rippled antiparallel and parallel β-sheet structures as well as the collagenic (three-strand) or polyglycine II-like (seven-strand) forms using density functional
Brett Harper et al.
Journal of the American Society for Mass Spectrometry, 25(10), 1716-1729 (2014-07-30)
It is shown that y-type ions, after losing C-terminal H2O or NH3, can lose an internal backbone carbonyl (CO) from different peptide positions and yield structurally different product fragment ions upon collision-induced dissociation (CID). Such CO losses from internal peptide
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