DL-Malic acid - AR, ≥99%(T) , CAS No.6915-15-7

Name: DL-Malic acid - AR, ≥99%(T) , CAS No.6915-15-7
Brand: Aladdin Scientific
SKU: M101126
Availability: InStock

CAS: 6915-15-7 Cat. No.: M101126 Summenformel: C₄H₆O₅ Molekulargewicht: 134.09 Beilstein Registry Number: 1723539 EG-Nummer: 230-022-8

249 Citations COA

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QUALITÄT & REINHEIT AR ? ≥99%(T)

Synonyms

DL-Hydroxybutanedioic acid | (±)-2-Hydroxysuccinic acid

Storage

Protected from light,Room temperature,Argon charged,Desiccated

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Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Warum diese Qualität

AR, ≥99%(T) AR für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Protected from light,Room temperature,Argon charged,Desiccated Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 249 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Spezifikationen

Synonyme

DL-Hydroxybutanedioic acid | (±)-2-Hydroxysuccinic acid

Spezifikationen & Reinheit

AR, ≥99%(T)

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Verschickt in

Normal

Note

Reinheit

≥99%(T)

Namen und Kennungen

Pubchem Sid

508810499

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810499

Kanonisches Lächeln

C(C(C(=O)O)O)C(=O)O

IUPAC Name

2-hydroxybutanedioic acid

InChIKey

BJEPYKJPYRNKOW-UHFFFAOYSA-N

INCHI

1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)

Isomere SMILES

C(C(C(=O)O)O)C(=O)O

WGK Deutschland

RTECS

ON7175000

Alternative CAS-Nummer

617-48-1

Molekulargewicht

134.09

Beilstein

1723539

Reaxy-Rn

1723539

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723539&ln=

Dokumentation

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Klasse Hydroxy acids and derivatives
    - Subclass Beta hydroxy acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Klasse	Hydroxy acids and derivatives
Subclass	Beta hydroxy acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Beta hydroxy acids and derivatives
Alternative Parents	Short-chain hydroxy acids and derivatives Fatty acids and conjugates Dicarboxylic acids and derivatives Alpha hydroxy acids and derivatives Secondary alcohols Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Short-chain hydroxy acid - Beta-hydroxy acid - Fatty acid - Dicarboxylic acid or derivatives - Alpha-hydroxy acid - Secondary alcohol - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.
External Descriptors	C4-dicarboxylic acid - 2-hydroxydicarboxylic 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

3D-Struktur

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PKD2L1 Tchem Polycystic kidney disease 2-like 1 protein (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

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

EGLN2 Tclin Hypoxia-inducible factor prolyl hydroxylase 1 (404 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

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

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

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

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

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

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

EGLN1 Tclin Egl nine homolog 1 (1702 Activities)

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EGLN3 Tclin Egl nine homolog 3 (250 Activities)

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

HIF1AN Tbio Hypoxia-inducible factor 1-alpha inhibitor (79 Activities)

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

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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

BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)

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FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)

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

Zugehörige Ziele (nicht menschlich)

ampC Beta-lactamase AmpC (62480 Activities)

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

Hdac6 Histone deacetylase 6 (222 Activities)

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

Plasmodium falciparum (966862 Activities)

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Meloidogyne incognita (862 Activities)

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

rep Replicase polyprotein 1ab (378 Activities)

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

Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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

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43 results found

Lot Number	Certificate Type	Datum	Artikel
J2619323	Certificate of Analysis	Aug 18, 2026	M101126
J2619306	Certificate of Analysis	Aug 18, 2026	M101126
H2631667	Certificate of Analysis	Aug 15, 2026	M101126
H2631651	Certificate of Analysis	Aug 15, 2026	M101126
H2631674	Certificate of Analysis	Aug 15, 2026	M101126
E2612353	Certificate of Analysis	Apr 30, 2026	M101126
E2612354	Certificate of Analysis	Apr 30, 2026	M101126
E2612355	Certificate of Analysis	Apr 30, 2026	M101126
J2516607	Certificate of Analysis	Aug 23, 2025	M101126
I2503790	Certificate of Analysis	Aug 23, 2025	M101126
I2503781	Certificate of Analysis	Aug 23, 2025	M101126
J2516608	Certificate of Analysis	Aug 23, 2025	M101126
J2516609	Certificate of Analysis	Aug 23, 2025	M101126
H2113239	Certificate of Analysis	May 12, 2025	M101126
E2513364	Certificate of Analysis	Apr 26, 2025	M101126
E2513365	Certificate of Analysis	Apr 26, 2025	M101126
E2513366	Certificate of Analysis	Apr 26, 2025	M101126
K2411455	Certificate of Analysis	Sep 25, 2024	M101126
K2411453	Certificate of Analysis	Sep 25, 2024	M101126
K2411454	Certificate of Analysis	Sep 25, 2024	M101126
D2521105	Certificate of Analysis	Jul 06, 2024	M101126
G2417138	Certificate of Analysis	Jul 03, 2024	M101126
G2417148	Certificate of Analysis	Jul 03, 2024	M101126
G2417136	Certificate of Analysis	Jul 03, 2024	M101126
D2416366	Certificate of Analysis	Mar 30, 2024	M101126
D2416362	Certificate of Analysis	Mar 30, 2024	M101126
D2416364	Certificate of Analysis	Mar 30, 2024	M101126
K2321505	Certificate of Analysis	Nov 08, 2023	M101126
K2321506	Certificate of Analysis	Nov 08, 2023	M101126
K2321511	Certificate of Analysis	Nov 08, 2023	M101126
I2305586	Certificate of Analysis	Aug 21, 2023	M101126
I2305585	Certificate of Analysis	Aug 21, 2023	M101126
I2305584	Certificate of Analysis	Aug 21, 2023	M101126
J2317053	Certificate of Analysis	Nov 24, 2022	M101126
C2317926	Certificate of Analysis	Nov 24, 2022	M101126
C2317892	Certificate of Analysis	Nov 24, 2022	M101126
C2317885	Certificate of Analysis	Nov 24, 2022	M101126
H2212317	Certificate of Analysis	Jul 22, 2022	M101126
H2212370	Certificate of Analysis	Jul 22, 2022	M101126
H2212307	Certificate of Analysis	Jul 22, 2022	M101126
B2216384	Certificate of Analysis	Dec 21, 2021	M101126
B2216419	Certificate of Analysis	Dec 21, 2021	M101126
B2216418	Certificate of Analysis	Dec 21, 2021	M101126

Chemische und physikalische Eigenschaften

Löslichkeit	Soluble in acetone, ether, water, methanol and ethanol.
Empfindlichkeit	Light sensitive.
Flammpunkt (°C)	203 °C
Schmelzpunkt (°C)	129-133°C
Molekulargewicht	134.090 g/mol
XLogP3	-1.300
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	3
Exact Mass	134.022 Da
Monoisotopic Mass	134.022 Da
Topological Polar Surface Area	94.800 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	129.000
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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DL-Malic acid - AR, ≥99%(T) , CAS No.6915-15-7

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DL-Malic acid - AR, ≥99%(T) , CAS No.6915-15-7

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