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Merck
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50280

Sigma-Aldrich

Gly-His hydrochloride hydrate

≥99.0% (calc. based on dry substance, AT)

Sinonimo/i:

Glycyl-L-histidine hydrochloride hydrate

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About This Item

Formula empirica (notazione di Hill):
C8H12N4O3 · HCl · xH2O
Numero CAS:
3486-76-8
Peso molecolare:
248.67 (anhydrous basis)
Beilstein:
3743779
Numero MDL:
MFCD00167964
Codice UNSPSC:
12352209
ID PubChem:
57651248
NACRES:
NA.22

Saggio

≥99.0% (calc. based on dry substance, AT)

Attività ottica

[α]20/D +31.5±1.0°, c = 2% in H2O (dry matter)

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Impurezze

~1 mol water

applicazioni

peptide synthesis

Stringa SMILE

O.Cl.NCC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O

InChI

1S/C8H12N4O3.ClH.H2O/c9-2-7(13)12-6(8(14)15)1-5-3-10-4-11-5;;/h3-4,6H,1-2,9H2,(H,10,11)(H,12,13)(H,14,15);1H;1H2/t6-;;/m0../s1
VGVLXWZHJBRECR-ILKKLZGPSA-N

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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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N Manoj et al.
The journal of peptide research : official journal of the American Peptide Society, 56(4), 210-217 (2000-11-18)
The crystal structures of the complexes of oxalic acid with glycyl-L-histidine and L-histidyl-L-alanine were determined. The three crystallographically independent peptide molecules in the complexes have closed conformations. The terminal carboxyl group of the dipeptide and the oxalate ion in the
Urszula Rychlewska et al.
Dalton transactions (Cambridge, England : 2003), 39(38), 8906-8913 (2010-08-21)
Monocationic gold(III) complexes with histidine-containing peptides, glycyl-L-histidine (Gly-L-His) and L-alanyl-L-histidine (L-Ala-L-His) have been synthesized and characterized by (1)H NMR spectroscopy and X-ray crystallography. The crystallized Au(III) complexes, [Au(Gly-L-His-N,N',N'')Cl]NO(3)·1.25H(2)O and [Au(L-Ala-L-His-N,N',N'')Cl]NO(3)·2.5H(2)O, were obtained from water solution at pH < 1.0. The
A Strauss et al.
FEMS microbiology letters, 127(3), 249-254 (1995-04-01)
A glycine-histidine tag (Gly3His6) was added to the C-terminus of a fusion protein consisting of the cholera toxin B-subunit (CtxB) and the IgA protease beta-domain (Iga beta). The aim was to facilitate single-step purification and to create a suitable tool
Michael S Kostelansky et al.
Biochemistry, 43(9), 2475-2483 (2004-03-03)
Structural analysis of recombinant fibrinogen fragment D revealed that the calcium-binding site (beta2-site) composed of residues BbetaAsp261, BbetaAsp398, BbetaGly263, and gammaGlu132 is modulated by the "B:b" interaction. To determine the beta2-site's role in polymerization, we engineered variant fibrinogen gammaE132A in
Girolamo Casella et al.
Inorganic chemistry, 47(11), 4796-4807 (2008-05-08)
We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data
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