A9627
Ala-Ala-Ala
≥98% (TLC)
Synonym(s):
Tri-L-alanine
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About This Item
Empirical Formula (Hill Notation):
C9H17N3O4
CAS Number:
Molecular Weight:
231.25
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
227-538-0
MDL number:
Product Name
Ala-Ala-Ala,
InChI key
BYXHQQCXAJARLQ-ZLUOBGJFSA-N
InChI
1S/C9H17N3O4/c1-4(10)7(13)11-5(2)8(14)12-6(3)9(15)16/h4-6H,10H2,1-3H3,(H,11,13)(H,12,14)(H,15,16)/t4-,5-,6-/m0/s1
SMILES string
C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(O)=O
assay
≥98% (TLC)
form
powder
color
white
storage temp.
−20°C
Quality Level
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Related Categories
Application
Trialanine (Ala-Ala-Ala) may be used along with other short chain alanines, tetra- and penta-alanine, as model compounds to study physicochemical parameters of small peptides.
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Fatma Eker et al.
Journal of the American Chemical Society, 125(27), 8178-8185 (2003-07-03)
Determination of the precise solution structure of peptides is of utmost importance to the understanding of protein folding and peptide drugs. Herein, we have measured the UV circular dichroism (UVCD) spectra of tri-alanine dissolved in D(2)O, H(2)O, and glycerol. The
Kwang-Im Oh et al.
Chirality, 22 Suppl 1, E186-E201 (2010-11-03)
Despite that a number of experimental and theoretical investigations have been carried out to determine the structure of trialanine in water, the reported populations of polyproline II (PPII) and β-strand conformers vary and were found to be dependent on which
Róisín Moriarty et al.
Thrombosis and haemostasis, 113(2), 290-304 (2014-11-22)
The integrin αIIbβ3 on resting platelets can bind to immobilised fibrinogen resulting in platelet spreading and activation but requires activation to bind to soluble fibrinogen. αIIbβ3 is known to interact with the general integrin-recognition motif RGD (arginine-glycine-aspartate) as well as
Mandy C Green et al.
The Journal of chemical physics, 138(7), 074111-074111 (2013-03-01)
An open-shell extension of the pair interaction energy decomposition analysis (PIEDA) within the framework of the fragment molecular orbital (FMO) method is developed. The open-shell PIEDA method allows the analysis of inter- and intramolecular interactions in terms of electrostatic, exchange-repulsion
Reinhard Schweitzer-Stenner
The journal of physical chemistry. B, 113(9), 2922-2932 (2009-02-27)
The conformational preference of individual amino acid residues in the unfolded state of peptides and proteins is the subject of a continuous debate. Research has mostly been focused on alanine, owing to its abundance in proteins and its relevance for
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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