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G5630

Sigma-Aldrich

Gly-Gly-Gly-Gly-Gly-Gly

solid

Sinonimo/i:

Hexaglycine

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About This Item

Formula empirica (notazione di Hill):
C12H20N6O7
Numero CAS:
3887-13-6
Peso molecolare:
360.32
Numero MDL:
MFCD00083697
Codice UNSPSC:
12352202
ID PubChem:
24895220
NACRES:
NA.26

product name

Gly-Gly-Gly-Gly-Gly-Gly,

Forma fisica

solid

Livello qualitativo

200

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)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Lys-Lys-Lys-Lys ≥95% (TLC)

Sigma-Aldrich

L9026

Lys-Lys-Lys-Lys

Triglycine United States Pharmacopeia (USP) Reference Standard

USP

1686386

Triglycine

Leu-Leu-Leu ≥90% (elemental analysis)

Sigma-Aldrich

L0879

Leu-Leu-Leu

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
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
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
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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