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DL-Aspartic acid - 98%, high purity , CAS No.617-45-8

13 Citations

COA

Grade & Purity:

≥98%

Cas Number: 617-45-8
Molecular Weight: 133.1
Beilstein Registry Number: 774618
MDL number: MFCD00063083
PubChem CID: 424
PubChem SID: 488179522

In stock

Item Number

A108708

Grouped product items
SKU	Size	Availability	Price
A108708-25g	25g	4	$9.90
A108708-100g	100g	3	$19.90
A108708-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$29.90

View related series

Chemical Biology (1255) Peptide chemistry (314)

Basic Description

Synonyms	DL-Asp-OH \| H-DL-Asp-OH \| DL-Aminosuccinic acid \| (+/-)-2-Aminosuccinic acid \| (+-)-Aspartic acid \| (R,S)-Aspartic acid \| 2-aminobutanedioic acid \| Aminosuccinic acid \| MFCD00063083 \| DL-Asparagic acid \| Acid D,L-aspart
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	DL-Aspartic acid (DL-Asp) is a racemic mixture of the proteinogenic amino acid L-aspartate and the non-proteinogenic amino acid D-aspartate. DL-Aspartic acid is used in studies on factors and conditions that enhance semen and sperm quality.
Storage Temp	Room temperature
Shipped In	Normal

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 Alpha amino acids and derivatives
        Level7 Aspartic acid 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 - Alpha amino acids and derivatives
Direct Parent	Aspartic acid and derivatives
Alternative Parents	Alpha amino acids Fatty acids and conjugates Dicarboxylic acids and derivatives Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Aspartic acid or derivatives - Alpha-amino acid - Dicarboxylic acid or derivatives - Fatty acid - Amino acid - Carboxylic acid - Hydrocarbon derivative - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic oxide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors	C4-dicarboxylic acid - alpha-amino 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

Names and Identifiers

Pubchem Sid	488179522
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488179522
IUPAC Name	2-aminobutanedioic acid
INCHI	InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)
InChIKey	CKLJMWTZIZZHCS-UHFFFAOYSA-N
Smiles	C(C(C(=O)O)N)C(=O)O
Isomeric SMILES	C(C(C(=O)O)N)C(=O)O
WGK Germany	1
RTECS	CI9097800
Molecular Weight	133.1
Beilstein	774618
Reaxy-Rn	774618
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774618&ln=

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.

18 results found

Lot Number	Certificate Type	Date	Item
I2412098	Certificate of Analysis	Aug 27, 2024	A108708
I2412099	Certificate of Analysis	Aug 27, 2024	A108708
I2412092	Certificate of Analysis	Aug 27, 2024	A108708
G2507113	Certificate of Analysis	Aug 27, 2024	A108708
I2412262	Certificate of Analysis	Aug 27, 2024	A108708
B2324349	Certificate of Analysis	Mar 02, 2023	A108708
I2217023	Certificate of Analysis	Mar 18, 2022	A108708
I2217025	Certificate of Analysis	Mar 18, 2022	A108708
A2425078	Certificate of Analysis	Mar 18, 2022	A108708
A2303330	Certificate of Analysis	Mar 18, 2022	A108708
I2217024	Certificate of Analysis	Mar 18, 2022	A108708
I2217027	Certificate of Analysis	Mar 18, 2022	A108708
H2412473	Certificate of Analysis	Mar 18, 2022	A108708
B2324353	Certificate of Analysis	Mar 18, 2022	A108708
H2308233	Certificate of Analysis	Mar 18, 2022	A108708
H2412502	Certificate of Analysis	Mar 18, 2022	A108708
C2413092	Certificate of Analysis	Mar 18, 2022	A108708
C2414076	Certificate of Analysis	Mar 18, 2022	A108708

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Chemical and Physical Properties

Solubility	Soluble in water, and hydrochloric acid. Insoluble in ether, and alcohol.
Sensitivity	Moisture sensitive.
Melt Point(°C)	300°C
Molecular Weight	133.100 g/mol
XLogP3	-2.800
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	3
Exact Mass	133.038 Da
Monoisotopic Mass	133.038 Da
Topological Polar Surface Area	101.000 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	133.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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