V2125
Val-Val
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About This Item
Empirical Formula (Hill Notation):
C10H20N2O3
CAS Number:
Molecular Weight:
216.28
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
storage temp.
−20°C
SMILES string
CC(C)C(N)C(=O)NC(C(C)C)C(O)=O
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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
Regulatory Information
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Joze Grdadolnik et al.
The journal of physical chemistry. B, 112(9), 2712-2718 (2008-02-12)
The NMR coupling constants ((3)J(H(N), H(alpha))) of dipeptides indicate that the backbone conformational preferences vary strikingly among dipeptides. These preferences are similar to those of residues in small peptides, denatured proteins, and the coil regions of native proteins. Detailed characterization
Alfredo E Cárdenas et al.
Biophysical journal, 85(5), 2919-2939 (2003-10-29)
An algorithm is described to compute approximate classical trajectories as a boundary value problem with an integration step in the arc length. High-frequency motions are filtered out when a large integration step is used, maintaining the stability of the algorithm.
W Bode et al.
European journal of biochemistry, 144(1), 185-190 (1984-10-01)
Large orthorhombic crystals of the complex formed by bovine trypsinogen and a semisynthetic homologous bovine pancreatic trypsin inhibitor with the reactive-site lysine residue replaced by an arginine residue [( Arg15]PTI) have been obtained which are isomorphous with the crystals of
R H Yun et al.
Protein engineering, 4(7), 761-766 (1991-10-01)
The conformational probability distribution of a valine residue in the valine dipeptide and of the valine side chain in an alpha-helix, as well as the change in helix stability for replacing alanine with valine, has been calculated by molecular dynamics
Kristof Plankensteiner et al.
Peptides, 26(7), 1109-1112 (2005-06-14)
The catalytic effects of the simple amino acid glycine on the formation of diproline and divaline in the prebiotically relevant salt-induced peptide formation (SIPF) reaction was investigated in systems of different amino acid starting concentrations and using the two enantiomeric
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