123188
5-Aminovaleric acid
97%, for peptide synthesis
Synonym(s):
5-AVA, 5-Aminopentanoic acid, Homopiperidinic acid
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About This Item
Linear Formula:
NH2(CH2)4CO2H
CAS Number:
Molecular Weight:
117.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
211-544-5
MDL number:
Beilstein/REAXYS Number:
906833
Product Name
5-Aminovaleric acid, 97%
InChI key
JJMDCOVWQOJGCB-UHFFFAOYSA-N
InChI
1S/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4,6H2,(H,7,8)
SMILES string
NCCCCC(O)=O
assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
158-161 °C (lit.)
application(s)
peptide synthesis
Quality Level
Gene Information
human ... SLC15A1(6564)
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Application
5-Aminovaleric acid (5-AVA) is used:
- In the preparation of (5-AVA)x(MA)1-xPbI3, a perovskite for fabricating printable mesoscopic perovskite solar cell.
- As a spacer in the synthesis of rhenium and technetium-99m labeled insulin.
- To synthesize dipeptides that self-assemble to form nanotubes in the solid state as well as in solution over a wide range of pH.
- As a starting material in the total synthesis of an alkaloid, lycoposerramine Z.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis and characterization of rhenium and technetium-99m labeled insulin.
Sundararajan C, et al.
Journal of Medicinal Chemistry, 53(6), 2612-2621 (2010)
Ariel Kwaka et al.
Molecular pharmacology, 94(5), 1289-1297 (2018-09-09)
Nematodes exhibit a vast array of cys-loop ligand-gated ion channels with unique pharmacologic characteristics. However, many of the structural components that govern the binding of various ligands are unknown. The nematode cys-loop GABA receptor uncoordinated 49 (UNC-49) is an important
cis-Decahydroquinolines via asymmetric organocatalysis: Application to the total synthesis of lycoposerramine Z.
Bradshaw B, et al.
Organic Letters, 15(2), 326-329 (2012)
A hole-conductor?free, fully printable mesoscopic perovskite solar cell with high stability.
Mei A, et al.
Science, 345(6194), 295-298 (2014)
G A van den Berg et al.
Journal of chromatography, 339(2), 223-231 (1985-05-03)
The mass fragmentographic identification of N-(2-carboxyethyl)-4-amino-n-butyric acid, N-(3-aminopropyl)-N1-(2-carboxyethyl)-1,4-diaminobutane, N,N1-bis(2-carboxyethyl)-1,4-diaminobutane, and delta-aminovaleric acid in acid-hydrolysed urines of a normal person and two cancer patients is described. A previous study, in which the metabolic fate of intraperitoneally injected polyamines in rats was
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