Name: Diacetylmonoxime - ≥98%(GC) , CAS No.57-71-6
SKU: D111029
Availability: InStock

Diacetylmonoxime - ≥98%(GC) , CAS No.57-71-6

CAS: 57-71-6 Cat. No.: D111029 Formule: C₄H₇NO₂ Poids moléculaire: 101.1 Beilstein Registry Number: 605582 Numéro CE: 200-348-5

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Diacetylmonoxime - ≥98%(GC) CAS No(57-71-6) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥98%(GC)

Synonyms

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble 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 FAQ et articles Citations of This Product Calculateurs de solution Avis

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Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

2,3-Butanedione monoxime has been used: · in single-molecule myosin V motility assays · as an anesthetic in the approach of imaging transgenic animals · to reduce rigor tension in muscle fibres · as a media component for mice cardiomyocytes culture

Specifications

Synonymes

Spécifications et pureté

≥98%(GC)

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%(GC)

Noms et identifiants

Pubchem Sid

504764111

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504764111

Sourires canoniques

CC(=NO)C(=O)C

IUPAC Name

(3E)-3-hydroxyiminobutan-2-one

InChIKey

FSEUPUDHEBLWJY-HWKANZROSA-N

INCHI

1S/C4H7NO2/c1-3(5-7)4(2)6/h7H,1-2H3/b5-3+

Isomères SMILES

C/C(=N\O)/C(=O)C

WGK Allemagne

RTECS

EK3150000

Poids moléculaire

101.1

Beilstein

605582

Reaxy-Rn

605582

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605582&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.

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📊 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 nitrogen compounds
  - Classe Organonitrogen compounds
    - Subclass Oximes

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Classe	Organonitrogen compounds
Subclass	Oximes
Intermediate Tree Nodes	Not available
Direct Parent	Ketoximes
Alternative Parents	Ketones Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Ketoxime - Ketone - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as ketoximes. These are organic compounds with the general formula RC(R')=NOH (R,R' = organyl).
External Descriptors	ketoxime
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)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

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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

PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)

Discover Target: PIN1

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

BLM Tchem Bloom syndrome protein (4248 Activities)

Discover Target: BLM

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

PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

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

Cibles associées (non humaines)

Saccharomyces cerevisiae (19171 Activities)

Explore this target

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

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

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

Npsr1 Neuropeptide S receptor (260 Activities)

Discover Target: Npsr1

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

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

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.

42 results found

Lot Number	Certificate Type	Date	Article
L2228032	Certificate of Analysis	Sep 22, 2026	D111029
H2612457	Certificate of Analysis	Apr 17, 2026	D111029
H2612447	Certificate of Analysis	Apr 17, 2026	D111029
H2612456	Certificate of Analysis	Apr 17, 2026	D111029
H2612483	Certificate of Analysis	Apr 17, 2026	D111029
C2625381	Certificate of Analysis	Mar 14, 2026	D111029
C2625419	Certificate of Analysis	Mar 14, 2026	D111029
C2625430	Certificate of Analysis	Mar 14, 2026	D111029
C2625433	Certificate of Analysis	Mar 14, 2026	D111029
J2509399	Certificate of Analysis	Sep 23, 2025	D111029
J2509400	Certificate of Analysis	Sep 23, 2025	D111029
J2509401	Certificate of Analysis	Sep 23, 2025	D111029
J2509402	Certificate of Analysis	Sep 23, 2025	D111029
E2527520	Certificate of Analysis	May 16, 2025	D111029
E2527511	Certificate of Analysis	May 16, 2025	D111029
E2527510	Certificate of Analysis	May 16, 2025	D111029
D2514061	Certificate of Analysis	Apr 28, 2025	D111029
J2415377	Certificate of Analysis	Sep 29, 2024	D111029
J2415368	Certificate of Analysis	Sep 29, 2024	D111029
J2415367	Certificate of Analysis	Sep 29, 2024	D111029
D2518224	Certificate of Analysis	Jun 26, 2024	D111029
D2518223	Certificate of Analysis	Jun 26, 2024	D111029
D2518222	Certificate of Analysis	Jun 26, 2024	D111029
C2412029	Certificate of Analysis	Apr 01, 2023	D111029
G2327182	Certificate of Analysis	Apr 01, 2023	D111029
G2327173	Certificate of Analysis	Apr 01, 2023	D111029
G2327168	Certificate of Analysis	Apr 01, 2023	D111029
G2327165	Certificate of Analysis	Apr 01, 2023	D111029
D2308913	Certificate of Analysis	Mar 17, 2023	D111029
D2308900	Certificate of Analysis	Mar 17, 2023	D111029
D2308899	Certificate of Analysis	Mar 17, 2023	D111029
B2328416	Certificate of Analysis	Feb 16, 2023	D111029
B2328415	Certificate of Analysis	Feb 16, 2023	D111029
B2328414	Certificate of Analysis	Feb 16, 2023	D111029
B2307136	Certificate of Analysis	Feb 11, 2023	D111029
B2307139	Certificate of Analysis	Feb 11, 2023	D111029
B2307137	Certificate of Analysis	Feb 11, 2023	D111029
L2228031	Certificate of Analysis	Nov 28, 2022	D111029
A2215457	Certificate of Analysis	Dec 29, 2021	D111029
A2215460	Certificate of Analysis	Dec 29, 2021	D111029
A2215459	Certificate of Analysis	Dec 29, 2021	D111029
A2215458	Certificate of Analysis	Dec 29, 2021	D111029

Propriétés chimiques et physiques

Solubilité	solubility in hot Water lmost transparency
Point d'ébullition (°C)	185-186°C
Point de fusion (°C)	76°C
Poids moléculaire	101.100 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	101.048 Da
Monoisotopic Mass	101.048 Da
Topological Polar Surface Area	49.700 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	106.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

FAQ et articles

Comparison of Urea Detection Methods: Reaction Mechanisms, Interference Factors, and Application Scenarios of the Urease Method and Diacetyl Monoxime Method

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

Tags:

Diacetyl monoxime method BUN DAM method GLDH-coupled method Urea Detection Urea Nitrogen Detection Urease Method Urease Serum Urea Urinary Urea Urea Standard Indophenol Colorimetric Method Ammonia Interference Colorimetric Method Clinical Biochemical Detection

Citations of This Product

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Avis

📚 Citations by Application

Organic synthesis — reaction medium12

Extraction & workup solvent6

Electrochemistry & battery electrolyte8

Other applications6

Cross-coupling reactions2

View all 16 citations →

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Produits apparentés

Diacetylmonoxime - AR , CAS No.57-71-6

Diacetylmonoxime - 10mM in DMSO , CAS No.57-71-6