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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 Summenformel: C2H2O2 Molekulargewicht: 58.04 Beilstein Registry Number: 1732463 EG-Nummer: 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
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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
Deutschland (EU)
USA*
Price
Qty
25ml
G103130-25ml
—
9 Auf Lager
117,93€
100ml
G103130-100ml
—
4 Auf Lager

353,08€

412,09€
Speichern 59,01 € (14.32%)
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen
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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

Synonyme
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-
Spezifikationen & Reinheit
Suitable for molecular biology, 40% in H2O(8.8 M)
Storage
Room temperature
Verschickt in
Normal
Note
Suitable for molecular biology
Namen und Kennungen
Pubchem Sid
488180588
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180588
Kanonisches Lächeln
C(=O)C=O
IUPAC Name
oxaldehyde
InChIKey
LEQAOMBKQFMDFZ-UHFFFAOYSA-N
INCHI
1S/C2H2O2/c3-1-2-4/h1-2H
Isomere SMILES
C(=O)C=O
WGK Deutschland
1
RTECS
MD2700000
UN-Nummer
2810
Verpackungsgruppe
I
Molekulargewicht
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.

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
KlasseOrganooxygen 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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
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
Zugehörige Ziele (nicht menschlich)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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 TypeDatumArtikel
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
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in ethanol and ether, soluble in water.
Brechungsindex1.3826
Siedepunkt (°C)104℃
Schmelzpunkt (°C)-14℃
Molekulargewicht58.040 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
FAQs und Artikel
Molecular Biology Grade
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Tags:
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The Skin Anti-Aging Mechanisms of α-Lipoic Acid: ALA/DHLA Redox Cycling, the Antioxidant Network, and Regulation of Collagen AGE Formation
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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:
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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
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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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