Name: Diacetylmonoxime - AR , CAS No.57-71-6
SKU: D111028
Availability: InStock

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

CAS: 57-71-6 Cat. No.: D111028 Formule: C₄H₇NO₂ Poids moléculaire: 101.1 Beilstein Registry Number: 605582 Numéro CE: 200-348-5

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Diacetylmonoxime - AR CAS No(57-71-6) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY AR ?

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 FAQ et articles Citations of This Product Calculateurs de solution Avis

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Why this grade

AR AR 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.

Specifications

Synonymes

Spécifications et pureté

Mécanismes biochimiques et physiologiques

Non-selective myosin ATPase inhibitor (K i = 5 mM at myosin II). Potent Kv2.1 (DRK1) and L-Type Ca 2+ channel inhibitor (K i and IC 50 values are 10.7 nM and 5.8 mM, respectively). Blood-brain barrier permeable. Inhibits muscle contraction.

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Noms et identifiants

Pubchem Sid

488195739

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488195739

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.

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 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)

Discover Target: THRB

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)

Discover Target: PMP22

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.

33 results found

Lot Number	Certificate Type	Date	Article
H2612446	Certificate of Analysis	Aug 19, 2026	D111028
H2612473	Certificate of Analysis	Aug 19, 2026	D111028
H2612482	Certificate of Analysis	Aug 19, 2026	D111028
C2625386	Certificate of Analysis	Mar 28, 2026	D111028
C2625406	Certificate of Analysis	Mar 28, 2026	D111028
C2625440	Certificate of Analysis	Mar 28, 2026	D111028
J2509398	Certificate of Analysis	Oct 16, 2025	D111028
J2509397	Certificate of Analysis	Oct 16, 2025	D111028
J2509332	Certificate of Analysis	Oct 16, 2025	D111028
J2119372	Certificate of Analysis	Aug 07, 2025	D111028
E2527512	Certificate of Analysis	Jun 07, 2025	D111028
E2527392	Certificate of Analysis	Jun 07, 2025	D111028
E2527530	Certificate of Analysis	Jun 07, 2025	D111028
J2415376	Certificate of Analysis	Oct 22, 2024	D111028
J2415378	Certificate of Analysis	Oct 22, 2024	D111028
J2415381	Certificate of Analysis	Oct 22, 2024	D111028
A2215414	Certificate of Analysis	Feb 05, 2024	D111028
K2320120	Certificate of Analysis	Nov 24, 2023	D111028
G2327164	Certificate of Analysis	Aug 03, 2023	D111028
G2327171	Certificate of Analysis	Aug 03, 2023	D111028
G2327177	Certificate of Analysis	Aug 03, 2023	D111028
D2308912	Certificate of Analysis	Apr 15, 2023	D111028
D2308910	Certificate of Analysis	Apr 15, 2023	D111028
D2308901	Certificate of Analysis	Apr 15, 2023	D111028
B2328417	Certificate of Analysis	Mar 07, 2023	D111028
B2328413	Certificate of Analysis	Mar 07, 2023	D111028
B2328412	Certificate of Analysis	Mar 07, 2023	D111028
B2328409	Certificate of Analysis	Mar 07, 2023	D111028
B2327022	Certificate of Analysis	Feb 18, 2023	D111028
B2314164	Certificate of Analysis	Feb 18, 2023	D111028
B2307138	Certificate of Analysis	Feb 14, 2023	D111028
B2315552	Certificate of Analysis	Jan 19, 2022	D111028
A2215415	Certificate of Analysis	Jan 19, 2022	D111028

Propriétés chimiques et physiques

Solubilité	Soluble in water; Soluble in Benzene,Chloroform,Ethanol,Ether,Acetone
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

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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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