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50280

Sigma-Aldrich

Gly-His hydrochloride hydrate

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

Synonym(s):

Glycyl-L-histidine hydrochloride hydrate

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About This Item

Empirical Formula (Hill Notation):
C8H12N4O3 · HCl · xH2O
CAS Number:
3486-76-8
Molecular Weight:
248.67 (anhydrous basis)
Beilstein:
3743779
MDL number:
MFCD00167964
UNSPSC Code:
12352209
PubChem Substance ID:
57651248
NACRES:
NA.22

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Assay

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

optical activity

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

reaction suitability

reaction type: solution phase peptide synthesis

impurities

~1 mol water

application(s)

peptide synthesis

SMILES string

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

InChI key

VGVLXWZHJBRECR-ILKKLZGPSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL4572
BCCH6228
BCBV6603
BCBP8541V
BCBJ4467V

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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
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
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
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
Giampiero De Sanctis et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 11(2), 153-167 (2005-12-13)
The pH dependence of redox properties, spectroscopic features and CO binding kinetics for the chelated protohemin-6(7)-L-histidine methyl ester (heme-H) and the chelated protohemin-6(7)-glycyl-L-histidine methyl ester (heme-GH) systems has been investigated between pH 2.0 and 12.0. The two heme systems appear
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