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Merck
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Documentos

G5630

Sigma-Aldrich

Gly-Gly-Gly-Gly-Gly-Gly

solid

Sinônimo(s):

Hexaglycine

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About This Item

Fórmula empírica (Notação de Hill):
C12H20N6O7
Número CAS:
3887-13-6
Peso molecular:
360.32
Número MDL:
MFCD00083697
Código UNSPSC:
12352202
ID de substância PubChem:
24895220
NACRES:
NA.26

product name

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

forma

solid

cor

white

pf

314.5 °C

aplicação(ões)

peptide synthesis

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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)

chave InChI

XJFPXLWGZWAWRQ-UHFFFAOYSA-N

Categorias relacionadas

Aplicação

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.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Lys-Lys-Lys-Lys ≥95% (TLC)

Sigma-Aldrich

L9026

Lys-Lys-Lys-Lys

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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