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

CAS: 107-22-2 Cat. No.: G103130 Formula: C2H2O2 Peso molecolare: 58.04 Beilstein Registry Number: 1732463 Numero EC: 203-474-9
198 Citations COA
Glyoxal solution - Suitable for molecular biology, 40% in H2O(8.8 M) CAS No(107-22-2) by Aladdin Scientific
Disponibile su ordine
GRADE & PURITY Suitable for molecular biology ? Molecular-biology grade — free of nucleases and contaminants that degrade DNA/RNA. Use in cloning, PCR, and nucleic-acid work needing clean reagents. 40% in H2O(8.8 M)
Synonyms
GLYOXAL|Ethanedial|107-22-2|Oxalaldehyde|oxaldehyde|1,2-Ethanedione|Biformyl|Diformyl|Glyoxylaldehyde|Biformal|Diformal|Oxal|Aerotex glyoxal 40|Glyoxal aldehyde|Ethanedione|CCRIS 952|Ethandial|HSDB 497|DTXSID5025364|Glyoxal, 29.2%|EINECS 203-474-9|ethane-
Storage
Room temperature
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
25ml
G103130-25ml
—
9 Disponibile
117,93€
100ml
G103130-100ml
—
4 Disponibile

353,08€

412,09€
Salva 59,01 € (14.32%)
Enter a quantity for the sizes you want to add.
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni
🧪
Why this grade

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

Specifications

Sinonimi
GLYOXAL | Ethanedial | 107-22-2 | Oxalaldehyde | oxaldehyde | 1,2-Ethanedione | Biformyl | Diformyl | Glyoxylaldehyde | Biformal | Diformal | Oxal | Aerotex glyoxal 40 | Glyoxal aldehyde | Ethanedione | CCRIS 952 | Ethandial | HSDB 497 | DTXSID5025364 | Glyoxal, 29.2% | EINECS 203-474-9 | ethane-
Specifiche e purezza
Suitable for molecular biology, 40% in H2O(8.8 M)
Condizioni di conservazione di stoccaggio
Room temperature
Spedito in
Normal
Grado
Suitable for molecular biology
Nomi e identificatori
Pubchem Sid
488180588
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180588
Sorrisi canonici
C(=O)C=O
IUPAC Name
oxaldehyde
InChIKey
LEQAOMBKQFMDFZ-UHFFFAOYSA-N
INCHI
1S/C2H2O2/c3-1-2-4/h1-2H
Isomeri SMILES
C(=O)C=O
WGK Germania
1
RTECS
MD2700000
Numero UN
2810
Gruppo di imballaggio
I
Peso molecolare
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=

Documentazione

📋 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

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree Nodes Aldehydes
Direct ParentShort-chain aldehydes
Alternative Parents Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Aliphatic acyclic compound
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPO Tchem Myeloperoxidase (1002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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 NumberCertificate TypeDataOggetto
I2608146Certificate of AnalysisSep 11, 2026 G103130
G2318198Certificate of AnalysisApr 09, 2025 G103130
D2117064Certificate of AnalysisOct 24, 2024 G103130
D2117066Certificate of AnalysisOct 24, 2024 G103130
I1804054Certificate of AnalysisJul 14, 2023 G103130
Proprietà chimiche e fisiche
SolubilitàSoluble in ethanol and ether, soluble in water.
Indice di rifrazione1.3826
Punto di ebollizione (°C)104℃
Punto di fusione (°C)-14℃
Peso molecolare58.040 g/mol
XLogP3-0.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass58.0055 Da
Monoisotopic Mass58.0055 Da
Topological Polar Surface Area34.100 Ų
Heavy Atom Count4
Formal Charge0
Complexity25.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Domande frequenti e articoli
Molecular Biology Grade
Categories: Reagent Specifications, Grading and Purity
Tags:
Grade Molecular Biology Grade
What Are the Differences Between Polyvinyl Alcohol 1788, 2488, and 2699? Understanding Workability, Bonding Strength, and Relative Water Resistance from the Perspective of Degree of Polymerization and Degree of Hydrolysis
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Paint Adhesive Water-soluble polymer materials Polymer materials
The Skin Anti-Aging Mechanisms of α-Lipoic Acid: ALA/DHLA Redox Cycling, the Antioxidant Network, and Regulation of Collagen AGE Formation
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
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
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
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
Tags:
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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Calcolatori di soluzioni
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