Skip to the beginning of the images gallery

L-Anserine Nitrate Salt - 98%, high purity , CAS No.10030-52-1

COA

Grade & Purity:

≥98%

Cas Number: 10030-52-1
Molecular Weight: 303.27
EC Number: 233-079-7
MDL number: MFCD00037001
PubChem CID: 112071
PubChem SID: 504756690

In stock

Item Number

L131686

Grouped product items
SKU	Size	Availability	Price
L131686-50mg	50mg	3	$108.90
L131686-250mg	250mg	3	$416.90
L131686-1g	1g	3	$1,497.90
L131686-5g	5g	2	$6,740.90

View related series

Metabolite (5307)

Basic Description

Synonyms	L-Anserine nitrate salt \| L-Anserine nitrate salt, hydroxyl radical scavenger \| (S)-2-(3-Aminopropanamido)-3-(1-methyl-1H-imidazol-5-yl)propanoicacidcompoundwithnitricacid(1:x) \| AKOS027250723 \| OLWOKAYJAHHSNY-QRPNPIFTSA-N \| EINECS 233-079-7 \| (S)-2-(3-Am
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	L-serine is a dipeptide found in most animal tissues. In the model system, it is an effective antioxidant and hydroxyl radical volatiles. Inhibition of aldose and ketosugar-induced nonenzymatic glycosylation. As an inhibitor of protein-protein cross-linki
Shipped In	Normal
Product Description	An antioxidant dipeptide.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Peptidomimetics
    - Subclass Hybrid peptides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Peptidomimetics
Subclass	Hybrid peptides
Intermediate Tree Nodes	Not available
Direct Parent	Hybrid peptides
Alternative Parents	Histidine and derivatives N-acyl-L-alpha-amino acids Beta amino acids and derivatives Imidazolyl carboxylic acids and derivatives N-substituted imidazoles Organic nitrates Heteroaromatic compounds Secondary carboxylic acid amides Organic nitro compounds Organic nitric acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Hybrid peptide - Histidine or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Imidazolyl carboxylic acid derivative - N-substituted imidazole - Heteroaromatic compound - Organic nitrate - Imidazole - Azole - Amino acid - Organic nitro compound - Secondary carboxylic acid amide - Organic nitric acid or derivatives - Organic nitric acid - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.
External Descriptors	Not available
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

Names and Identifiers

Pubchem Sid	504756690
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756690
IUPAC Name	(2S)-2-(3-aminopropanoylamino)-3-(3-methylimidazol-4-yl)propanoic acid;nitric acid
INCHI	InChI=1S/C10H16N4O3.HNO3/c1-14-6-12-5-7(14)4-8(10(16)17)13-9(15)2-3-11;2-1(3)4/h5-6,8H,2-4,11H2,1H3,(H,13,15)(H,16,17);(H,2,3,4)/t8-;/m0./s1
InChIKey	OLWOKAYJAHHSNY-QRPNPIFTSA-N
Smiles	CN1C=NC=C1CC(C(=O)O)NC(=O)CCN.[N+](=O)(O)[O-]
Isomeric SMILES	CN1C=NC=C1C[C@@H](C(=O)O)NC(=O)CCN.[N+](=O)(O)[O-]
WGK Germany	3
PubChem CID	112071
Molecular Weight	303.27

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

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

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number	Certificate Type	Date	Item
F2201216	Certificate of Analysis	Mar 14, 2024	L131686
F2201058	Certificate of Analysis	Mar 14, 2024	L131686
F2201059	Certificate of Analysis	Mar 14, 2024	L131686
I1529089	Certificate of Analysis	Mar 17, 2023	L131686

Chemical and Physical Properties

Solubility	Soluble in Water.
Molecular Weight	303.270 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	6
Exact Mass	303.118 Da
Monoisotopic Mass	303.118 Da
Topological Polar Surface Area	176.000 Å²
Heavy Atom Count	21
Formal Charge	0
Complexity	309.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
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	2

Documents & Articles

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration