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2,5-Hexanedione - analytical standard, ≥99.5%(GC) , CAS No.110-13-4

2,5-Hexanedione - analytical standard, ≥99.5%(GC) , CAS No.110-13-4

Name: 2,5-Hexanedione - analytical standard, ≥99.5%(GC) , CAS No.110-13-4
SKU: H106699
Availability: InStock

CAS: 110-13-4 Cat. No.: H106699 Formule: C₆H₁₀O₂ Poids moléculaire: 114.14 Beilstein Registry Number: 506525 Numéro CE: 203-738-3

18 Citations COA

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2,5-Hexanedione - analytical standard, ≥99.5%(GC) CAS No(110-13-4) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY Analytical standard ? ≥99.5%(GC)

Synonyms

Storage

Room temperature

Shipped In

Normal

Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Citations of This Product Calculateurs de solution Avis

🧪

Why this grade

analytical standard, ≥99.5%(GC) Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 18 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes

Spécifications et pureté

analytical standard, ≥99.5%(GC)

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

Analytical standard

Pureté

≥99.5%(GC)

Noms et identifiants

Pubchem Sid

528755593

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528755593

Sourires canoniques

CC(=O)CCC(=O)C

IUPAC Name

hexane-2,5-dione

InChIKey

OJVAMHKKJGICOG-UHFFFAOYSA-N

INCHI

1S/C6H10O2/c1-5(7)3-4-6(2)8/h3-4H2,1-2H3

Isomères SMILES

CC(=O)CCC(=O)C

WGK Allemagne

RTECS

MO3150000

Numéro ONU

1224

Groupe d'emballage

Poids moléculaire

114.14

Beilstein

506525

Reaxy-Rn

506525

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506525&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
  - Classe Organooxygen compounds
    - Subclass Carbonyl compounds

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Classe	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Not available
Direct Parent	Ketones
Alternative Parents	Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
External Descriptors	Oxygenated hydrocarbons
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

Structure 3D

Cibles associées (humaines)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

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

Discover Target: APEX1

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

Cibles associées (non humaines)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

1 results found

Lot Number	Certificate Type	Date	Article
H1305014	Certificate of Analysis	Jul 07, 2026	H106699

Propriétés chimiques et physiques

Solubilité	Easily soluble in water and most organic solvents.
Indice de réfraction	1.425
Point d'éclair (°F)	174.2 ℉
Point d'éclair (°C)	79 ℃
Point d'ébullition (°C)	191°C
Point de fusion (°C)	-6--5°C
Poids moléculaire	114.140 g/mol
XLogP3	-0.300
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	3
Exact Mass	114.068 Da
Monoisotopic Mass	114.068 Da
Topological Polar Surface Area	34.100 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	91.100
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

Citations of This Product

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Avis

📚 Citations by Application

Organic synthesis — reaction medium18

Extraction & workup solvent7

Industrial & non-pharma application4

Cross-coupling reactions6

Drug / compound screening2

Electrochemistry & battery electrolyte1

Polymer synthesis & polymerization1

Chromatography (HPLC / GC / TLC)1

Other applications3

View all 18 citations →

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