Skip to the beginning of the images gallery

Asparagusic acid - ≥96.0%, high purity , CAS No.2224-02-4

COA

Grade & Purity:

≥96%

Cas Number: 2224-02-4
Molecular Weight: 150.2
PubChem CID: 16682

In stock

Item Number

A648400

Grouped product items
SKU	Size	Availability	Price
A648400-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$84.90
A648400-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$132.90
A648400-50mg	50mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$324.90
A648400-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$487.90

Ketones, Aldehydes, Acids

View related series

Acids (103) Aldehydes (60) Anti-infection (2803) Ketones (57) Metabolite (5307) Parasite (997)

Basic Description

Synonyms	PH-800/21 \| AKOS006277672 \| D82957 \| HY-50730 \| 1,2-DITHIACYCLOPENTANE-4-CARBOXYLIC ACID \| Asparagusic acid \| BRN 0112178 \| PH 800/21 \| C01892 \| DTXSID00176779 \| VAD3XV509R \| 1,2-DITHIOLANE-4-CARBOXYLIC ACID \| A901670 \| 1,2-Dithiolan-4-carbonsA currencyur
Specifications & Purity	≥96%
Biochemical and Physiological Mechanisms	Asparagusic acid is a sulfur-containing flavor component produced by Asparagus officinalis Linn., with anti-parasitic effect. Asparagusic acid is a plant growth inhibitor.
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Asparagusic acid is a sulfur-containing flavor component produced by Asparagus officinalis Linn., with anti-parasitic effect. Asparagusic acid is a plant growth inhibitor In Vitro Asparagusic acid is toxic to several plant parasitic nematodes and would be a major factor in resistance of asparagus. Asparagusic acid inhibits growth in lettuce and other seedlings at 6.67×10 -7 M to 6.67×10 -7 M. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:Human Endogenous Metabolite

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Dithiolanes
    - Subclass Dithiolanecarboxylic acids
      - Level5 1,2-dithiolanecarboxylic acids
        Level6 1,2-dithiolane-4-carboxylic acids

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Dithiolanes
Subclass	Dithiolanecarboxylic acids
Intermediate Tree Nodes	1,2-dithiolanecarboxylic acids
Direct Parent	1,2-dithiolane-4-carboxylic acids
Alternative Parents	1,2-dithiolanes Organic disulfides Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	1,2-dithiolane-4-carboxylic acid - 1,2-dithiolane - Organic disulfide - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as 1,2-dithiolane-4-carboxylic acids. These are organic compounds containing a 1,2-dithiolane ring that bears a carboxylic acid group at the 4-position.
External Descriptors	dithiolanes - sulfur-containing carboxylic acid - dithiolanecarboxylic acid
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

Mechanisms of Action

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

Names and Identifiers

IUPAC Name	dithiolane-4-carboxylic acid
INCHI	InChI=1S/C4H6O2S2/c5-4(6)3-1-7-8-2-3/h3H,1-2H2,(H,5,6)
InChIKey	AYGMEFRECNWRJC-UHFFFAOYSA-N
Smiles	C1C(CSS1)C(=O)O
Isomeric SMILES	C1C(CSS1)C(=O)O
PubChem CID	16682
Molecular Weight	150.2

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

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

Analytical Chart:

Chemical and Physical Properties

Solubility	DMSO : ≥ 46 mg/mL (306.22 mM)
Molecular Weight	150.200 g/mol
XLogP3	0.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	1
Exact Mass	149.981 Da
Monoisotopic Mass	149.981 Da
Topological Polar Surface Area	87.900 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	98.200
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

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