Suitable for molecular biology, 40% in H2O(8.8 M) Suitable for molecular biology 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 198 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos

Especificações e pureza

Suitable for molecular biology, 40% in H2O(8.8 M)

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Grau

Suitable for molecular biology

Nomes e identificadores

Pubchem Sid

488180588

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180588

Sorrisos canónicos

C(=O)C=O

IUPAC Name

oxaldehyde

InChIKey

LEQAOMBKQFMDFZ-UHFFFAOYSA-N

INCHI

1S/C2H2O2/c3-1-2-4/h1-2H

SMILES isoméricas

C(=O)C=O

WGK Alemanha

RTECS

MD2700000

Número UN

2810

Grupo de embalagem

Peso molecular

58.04

Beilstein

1732463

Reaxy-Rn

1732463

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732463&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 oxygen compounds
  - Classe Organooxygen compounds
    - Subclass Carbonyl compounds
      - Level5 Aldehydes
        Level6 Short-chain aldehydes

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Classe	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Aldehydes
Direct Parent	Short-chain aldehydes
Alternative Parents	Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Aliphatic acyclic compound
Descrição	This compound belongs to the class of organic compounds known as short-chain aldehydes. These are an aldehyde with a chain length containing between 2 and 5 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

Estrutura 3D

Alvos associados (humanos)

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

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

MPO Tchem Myeloperoxidase (1002 Activities)

Discover Target: MPO

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

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

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

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

Alvos associados (não humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mecanismos de ação

Certificados（CoA,COO,BSE/TSE e Mapa de Análise)

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.

5 results found

Lot Number	Certificate Type	Data	Item
I2608146	Certificate of Analysis	Sep 11, 2026	G103130
G2318198	Certificate of Analysis	Apr 09, 2025	G103130
D2117064	Certificate of Analysis	Oct 24, 2024	G103130
D2117066	Certificate of Analysis	Oct 24, 2024	G103130
I1804054	Certificate of Analysis	Jul 14, 2023	G103130

Propriedades químicas e físicas

Solubilidade	Soluble in ethanol and ether, soluble in water.
Índice de refração	1.3826
Ponto de ebulição (°C)	104℃
Ponto de fusão (°C)	-14℃
Peso molecular	58.040 g/mol
XLogP3	-0.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	58.0055 Da
Monoisotopic Mass	58.0055 Da
Topological Polar Surface Area	34.100 Å²
Heavy Atom Count	4
Formal Charge	0
Complexity	25.000
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 e artigos

Molecular Biology Grade

Categories: Reagent Specifications, Grading and Purity

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Grade Molecular Biology Grade

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Antioxidant Glycation reaction

Skin Anti-Aging Mechanisms of Carnosine and Decarboxy Carnosine: Active Carbonyl Scavenging, Oxidative-Stress Buffering, and Inhibition of Collagen Glycation Cross-Linking

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Carnosine β-alanine L-histidine

How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis

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

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Extracellular matrix Fibroblasts stratum corneum delivery collagen tripeptide (CTP) Gly–X–Y sequence stratum corneum hydration matrix protection collagen homeostasis

What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling

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

Tags:

Collagen

Storage Stability and Deoxyfluorination Reactivity of ImCl[H₂F₃]—Reactivity Modulation of the H₂F₃⁻ Fluoride Source and Substrate Activation by 2-Chloroimidazolium

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

Tags:

Deoxyfluorination

Citations of This Product

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Revisões

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Glyoxal solution - Suitable for molecular biology, 40% in H2O(8.8 M) , CAS No.107-22-2

Storage & shipping

Quality documents

Literature proof

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

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