Name: 2,3-Butanedione - ≥97% , CAS No.431-03-8
SKU: B432715
Availability: InStock

2,3-Butanedione - ≥97% , CAS No.431-03-8

CAS: 431-03-8 Cat. No.: B432715 Summenformel: C₄H₆O₂ Molekulargewicht: 86.09 Beilstein Registry Number: 1769 EG-Nummer: 207-069-8

Zum Ende der Bildgalerie springen

2,3-Butanedione - ≥97% CAS No(431-03-8) by Aladdin Scientific

Zum Anfang der Bildgalerie springen

Zu bestellen verfügbar

GRADE & PURITY ≥97%

Synonyms

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Übersicht Specifications Namen und Kennungen Documentation Advanced Data 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

🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice,FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 54 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Gene Information

human ... ACHE(43.Flammable liquid), BCHE(590), CES1(1066)

Application

Inactivates aminopeptidase-N. Cyclocondensation with amines has been used to form triazine and pteridine ring systems. Also used as a precursor to α-diones.

Specifications

Synonyme

Spezifikationen & Reinheit

≥97%

Storage

Store at 2-8°C

Verschickt in

Wet ice,FedEx DG Service

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥97%

Namen und Kennungen

Pubchem Sid

508807630

Kanonisches Lächeln

CC(=O)C(=O)C

IUPAC Name

butane-2,3-dione

InChIKey

QSJXEFYPDANLFS-UHFFFAOYSA-N

INCHI

1S/C4H6O2/c1-3(5)4(2)6/h1-2H3

Isomere SMILES

CC(=O)C(=O)C

WGK Deutschland

RTECS

EK2625000

UN-Nummer

2346

Verpackungsgruppe

Molekulargewicht

86.09

Beilstein

1769

Reaxy-Rn

605398

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605398&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Klasse Organooxygen compounds
    - Subclass Carbonyl compounds
      - Ebene5 Ketones
        Ebene6 Alpha-diketones

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Klasse	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Ketones
Direct Parent	Alpha-diketones
Alternative Parents	Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alpha-diketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as alpha-diketones. These are organic compounds containing two ketone groups on two adjacent carbon atoms.
External Descriptors	a small molecule
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

Zugehörige Ziele (menschlich)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

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

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

BCHE Tclin Butyrylcholinesterase (7174 Activities)

Discover Target: BCHE

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

ARSA Tbio Cerebroside-sulfatase (655 Activities)

Discover Target: ARSA

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

CES2 Tchem Carboxylesterase 2 (583 Activities)

Discover Target: CES2

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

CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)

Discover Target: CES1

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

ACLY Tclin ATP-citrate synthase (168 Activities)

Discover Target: ACLY

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)

Discover Target: EHMT2

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

THPO Tbio Thrombopoietin (834 Activities)

Discover Target: THPO

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

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

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

Zugehörige Ziele (nicht menschlich)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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

Impa1 Inositol monophosphatase 1 (16203 Activities)

Discover Target: Impa1

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

nfo Endonuclease 4 (425 Activities)

Discover Target: nfo

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

crtY Lycopene cyclase (9 Activities)

Discover Target: crtY

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):

Analytical Chart:

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

9 results found

Lot Number	Certificate Type	Datum	Artikel
F2612366	Certificate of Analysis	Jun 25, 2026	B432715
F2612398	Certificate of Analysis	Jun 25, 2026	B432715
G2609104	Certificate of Analysis	Jun 25, 2026	B432715
K2528041	Certificate of Analysis	Dec 03, 2025	B432715
L2505084	Certificate of Analysis	Dec 03, 2025	B432715
J2430411	Certificate of Analysis	Nov 02, 2024	B432715
J2430752	Certificate of Analysis	Nov 02, 2024	B432715
B2401061	Certificate of Analysis	Feb 20, 2024	B432715
B2401062	Certificate of Analysis	Feb 20, 2024	B432715

Chemische und physikalische Eigenschaften

Brechungsindex	1.394
Flammpunkt (°C)	7 °C
Siedepunkt (°C)	88°C
Schmelzpunkt (°C)	-4 °C
Molekulargewicht	86.090 g/mol
XLogP3	-1.300
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	86.0368 Da
Monoisotopic Mass	86.0368 Da
Topological Polar Surface Area	34.100 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	71.500
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

FAQs und Artikel

Why Bicyclo[1.1.1]pentane (BCP) Has Become an Important Medicinal Chemistry Building Block: Phenyl Ring Replacement, Strain Release, and Functional-Group Interfaces

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

BCP

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Lösungsrechner

Molarity Calculator

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

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Reconstitution Calculator

Bewertungen

📚 Citations by Application

Extraction & workup solvent11

Organic synthesis — reaction medium27

Spectroscopy sample preparation9

Polymer synthesis & polymerization3

Drug / compound screening7

Other applications26

Chromatography (HPLC / GC / TLC)10

Controlled-release & nanoparticle carrier3

Cell viability1

Electrochemistry & battery electrolyte3

Cross-coupling reactions1

IC50 determination1

Cytotoxicity screening1

Cancer cell line characterization1

Industrial & non-pharma application1

Nanoparticle / material biocompatibility1

View all 54 citations →

Bulk & Custom Packaging Need larger quantities or custom specifications? Contact our team for a tailored quote.