Basic Description

Synonyms	5-AVA \| 5-aminovalerate \| RS-1002 \| AM82459 \| NCGC00014991-05 \| EINECS 211-544-5 \| EN300-28602 \| FT-0620031 \| 5-amino valeric acid \| Lopac0_000031 \| Homopiperidinic acid \| NSC58383 \| NSC-58383 \| Spectrum3_001447 \| CHEBI:15887 \| 5-aminopentanoate \| delta-A
Specifications & Purity	≥97%
Shipped In	Normal
Product Description	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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Delta amino acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives
Direct Parent	Delta amino acids and derivatives
Alternative Parents	Straight chain fatty acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Delta amino acid or derivatives - Straight chain fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as delta amino acids and derivatives. These are compounds containing a carboxylic acid group and an amino group at the C5 carbon atom.
External Descriptors	Amino fatty acids
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

SLC6A1 Tclin GABA transporter 1 (308 Activities)

Discover Target: SLC6A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC15A1 Tchem Oligopeptide transporter small intestine isoform (922 Activities)

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ARSA Tbio Cerebroside-sulfatase (655 Activities)

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SLC6A11 Tchem GABA transporter 3 (176 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

Discover Target: NFKB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

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CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

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CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

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GABRR1 Tchem GABA receptor rho-1 subunit (233 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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Associated Targets(non-human)

Slc6a11 GABA transporter 4 (930 Activities)

Discover Target: Slc6a11

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pfk 6-phospho-1-fructokinase (7870 Activities)

Discover Target: pfk

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488179493
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488179493
IUPAC Name	5-aminopentanoic acid
INCHI	InChI=1S/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4,6H2,(H,7,8)
InChIKey	JJMDCOVWQOJGCB-UHFFFAOYSA-N
Smiles	C(CCN)CC(=O)O
Isomeric SMILES	C(CCN)CC(=O)O
WGK Germany	3
Molecular Weight	117.15
Beilstein	906833
Reaxy-Rn	906833
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=906833&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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17 results found

Lot Number	Certificate Type	Date	Item
G2121023	Certificate of Analysis	May 09, 2025	A107493
K2408126	Certificate of Analysis	Mar 14, 2024	A107493
D2403671	Certificate of Analysis	Mar 14, 2024	A107493
B2324294	Certificate of Analysis	Mar 02, 2023	A107493
B2324295	Certificate of Analysis	Mar 02, 2023	A107493
B2324296	Certificate of Analysis	Mar 02, 2023	A107493
E1519024	Certificate of Analysis	Feb 09, 2023	A107493
K2408121	Certificate of Analysis	Aug 03, 2022	A107493
K2408123	Certificate of Analysis	Aug 03, 2022	A107493
I2318172	Certificate of Analysis	Aug 03, 2022	A107493
I2216086	Certificate of Analysis	Aug 03, 2022	A107493
I2216087	Certificate of Analysis	Aug 03, 2022	A107493
I2216088	Certificate of Analysis	Aug 03, 2022	A107493
I2216089	Certificate of Analysis	Aug 03, 2022	A107493
L2321122	Certificate of Analysis	Aug 03, 2022	A107493
B2426251	Certificate of Analysis	Aug 03, 2022	A107493
K2408122	Certificate of Analysis	Aug 03, 2022	A107493

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Chemical and Physical Properties

Melt Point(°C)	158-161°C
Molecular Weight	117.150 g/mol
XLogP3	-2.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	117.079 Da
Monoisotopic Mass	117.079 Da
Topological Polar Surface Area	63.300 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	72.800
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Jianan Chen, Zhaobing Tang, Yangzhou Zhou, Ting Zhang, Lei Qian, Chaoyu Xiang. (2023) In-situ solution processed zinc Oxide as electron transport layer for High-performance perovskite Light-emitting diodes. CHEMICAL PHYSICS LETTERS, 819 (140441).
2. Hongyu Xu, Yuanzhi Jiang, Tingwei He, Saisai Li, Huanhua Wang, Yu Chen, Mingjian Yuan, Jun Chen. (2019) Orientation Regulation of Tin-Based Reduced-Dimensional Perovskites for Highly Efficient and Stable Photovoltaics. ADVANCED FUNCTIONAL MATERIALS, 29 (47): (1807696).
3. Guolin Zhang, Runqing Lu, Ziping Liu, Kaijie Ni, Tao Jiang, Xiangru Tao, Guanhaojie Zheng, Chang Yi, Jianpu Wang. (2024) Pure-Phase Perovskite Quantum Well for Green Light-Emitting Diodes. ACS Applied Materials & Interfaces, 16 (38): (51195-51200).
4. Yunhui Kuang, Yazhuo Xue, Zheng Zhang, Lvpeng Yang, Tong Bie, Rui Li, Wenxi Liang, Naigen Zhou, Ming Shao. (2025) Strategic regulation of crystallization kinetics to achieve efficient pure-red quasi-2D perovskite light-emitting diodes. CHEMICAL ENGINEERING JOURNAL, 507 (160278).

Solution Calculators

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SKU	Size	Availability	Price
A107493-1g	1g	4	$13.90
A107493-5g	5g	5	$50.90
A107493-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$91.90
A107493-25g	25g	4	$148.90
A107493-100g	100g	1	$533.90

5-Aminovaleric acid - 97%, high purity , CAS No.660-88-8