Ascorbic acid - Moligand™, suitable for plant cell culture , CAS No.50-81-7

CAS: 50-81-7 Cat. No.: A103540 Formula: C6H8O6 Peso molecolare: 176.12 Beilstein Registry Number: 84272 Numero EC: 200-066-2
Disponibile su ordine
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Suitable for plant cell culture ? Plant cell-culture grade — formulated for plant tissue and cell cultures. Use in plant biotechnology, callus, and suspension culture work.
Synonyms
Ascorbicap | C-Long | Ferrous ascorbate | phosphorus oxichloride | Ceglion | Cenetone | Cetemican | hexamethyl-disiloxane | Ascorb | Cemagyl | Cipca | Planavit C | Secorbate | Vitacee | Ascorbicab | Scorbacid | Cecon | C-Span | Duoscorb | pentakis(chloran
Storage
Protected from light,Room temperature,Desiccated
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
100g
A103540-100g
3 Disponibile
5 Disponibile

73,67€

85,82€
Salva 12,15 € (14.16%)
500g
A103540-500g
1 Disponibile
2 Disponibile

306,23€

357,42€
Salva 51,20 € (14.32%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

Moligand™, suitable for plant cell culture Adatto alla coltura di cellule vegetali,Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Desiccated 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 4238 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
Ascorbicap | C-Long | Ferrous ascorbate | phosphorus oxichloride | Ceglion | Cenetone | Cetemican | hexamethyl-disiloxane | Ascorb | Cemagyl | Cipca | Planavit C | Secorbate | Vitacee | Ascorbicab | Scorbacid | Cecon | C-Span | Duoscorb | pentakis(chloran
Specifiche e purezza
Moligand™, suitable for plant cell culture
Meccanismi biochimici e fisiologici
L-ascorbic acid mainly has antioxidant properties. It protects plants from oxidative stress and mammals from diseases related to oxidative stress. L-ascorbic acid mainly plays a protective role against hydroxyl radicals, superoxide, and singlet oxygen. In
Condizioni di conservazione di stoccaggio
Protected from light,Room temperature,Desiccated
Spedito in
Normal
Grado
Adatto alla coltura di cellule vegetali, Moligand™
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508813560
Sorrisi canonici
OC([C@]([C@@H](O)CO)([H])O1)=C(O)C1=O
IUPAC Name
(2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one
InChIKey
CIWBSHSKHKDKBQ-JLAZNSOCSA-N
INCHI
1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5+/m0/s1
Isomeri SMILES
C([C@@H]([C@@H]1C(=C(C(=O)O1)O)O)O)O
WGK Germania
1
RTECS
CI7650000
CAS alternativo
53262-66-1,6730-29-6,50-81-7,134-03-2 (monosodium salt)
Numero NSC
UN 1648
Numero UN
3
Termini MeSH
Acid, Ascorbic;Acid, L-Ascorbic;Ascorbate, Ferrous;Ascorbate, Magnesium;Ascorbate, Sodium;Ascorbic Acid;Ascorbic Acid, Monosodium Salt;di-L-Ascorbate, Magnesium;Ferrous Ascorbate;Hybrin;L Ascorbic Acid;L-Ascorbic Acid;Magnesium Ascorbate;Magnesium Ascorbi
Peso molecolare
176.12
Beilstein
84272
Reaxy-Rn
84272
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=84272&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
SuperclassOrganoheterocyclic compounds
ClasseDihydrofurans
SubclassFuranones
Intermediate Tree Nodes Not available
Direct ParentButenolides
Alternative Parents Vinylogous acids  Enoate esters  Secondary alcohols  Lactones  Enediols  1,2-diols  Oxacyclic compounds  Monocarboxylic acids and derivatives  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents 2-furanone - Vinylogous acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - 1,2-diol - Carboxylic acid ester - Enediol - Secondary alcohol - Lactone - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Primary alcohol - Organooxygen compound - Aliphatic heteromonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.
External Descriptors Water-soluble vitamins
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
ADRA2B Tclin Alpha-2B adrenergic receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 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.

7 results found

Lot NumberCertificate TypeDataOggetto
F2611169Certificate of AnalysisJun 23, 2026 A103540
F1820087Certificate of AnalysisJan 27, 2026 A103540
J2514085Certificate of AnalysisOct 20, 2025 A103540
J2116390Certificate of AnalysisJul 15, 2025 A103540
J2116392Certificate of AnalysisJul 15, 2025 A103540
A2331221Certificate of AnalysisSep 22, 2021 A103540
I2403060Certificate of AnalysisSep 22, 2021 A103540
Proprietà chimiche e fisiche
SensibilitàLight sensitive.
Rotazione specifica [α]21 ° (C=10, H2O)
Punto di fusione (°C)190-192°C
Peso molecolare176.120 g/mol
XLogP3-1.600
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass176.032 Da
Monoisotopic Mass176.032 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity232.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
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
For Cell Culture
Suitable for Plant Cell Culture
EdU Staining: Basic Principle and Experimental Workflow
Bio-based Chemicals: From Platform Molecules to Application Scenarios — Trend Insights and Aladdin’s Product Portfolio
Nanowires: Properties, Preparation Routes, and Process Selection (Comprehensive Analysis of Top-Down and Bottom-Up Approaches with Recommended Aladdin Reagents)
Tyrosinase: a key regulatory enzyme in melanin synthesis and its biological and applied significance
Installing a Redox Switch on Biomolecules: Principles, Conjugation Essentials, and an Application Guide for ATTO MB2 NHS ester
Functions and Significance of Common Physiological and Biochemical Indices in Animals and Plants
How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)
Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics
Lipid Panel Testing in Research (TC, TG, HDL-C, LDL-C): Indicator System, Assay Principles, Technical Routes, and Application Overview
Glucose Content Determination: A Systematic Review of Detection Principles, Method Validation, and Research Application Frameworks
Procyanidins: Structural Features and Key Points for Research and Application
Phytase: Enzymological Properties, Mechanism of Action, and Applications in Feed and Food
Chlorophyll: Structural Features, Physicochemical Properties, and Key Points for Research and Industrial Applications
Ferulic Acid: Structural Features, Preparation Routes, and Key Points for Research Applications
Physicochemical Properties of Diphenylamine, Analytical Applications, and a Review of Its DNA Colorimetric Reaction
Review of Glucose-6-phosphate Dehydrogenase (G6PD): Structural Features, Metabolic Functions, and Research Applications
Review of the Structural Characteristics, Biological Functions, and Application Advances of Lycopene
Analytical Basis, Methodological Systems, and Quality Control for Vitamin C Content Determination
Antioxidant Enzyme Networks in Skin Cells and Their Applications in Skincare and Cosmetics
Progress in Research on Sugar-Nucleotide Metabolism Related to Ascorbate Biosynthesis in Plants
Galactose-Related Precursor Conversion and Redox Regulation in Plant Ascorbate Biosynthesis
Coupling Mechanisms Between Terminal Reducing-Power Allocation in Photosynthetic Electron Transport and Metabolic Demand
Research Progress on the Moonlighting Functions of Carbohydrate-Metabolic Enzymes in Replication Programs, DNA Damage Repair, and Inflammatory Activation
Mechanisms and Experimental Applications of β-GP, Ascorbic Acid, and Dexamethasone in Osteogenic Induction Systems
Enzymatic Hydroxylation Mechanism of Salicylate Conversion to Catechol
Waterborne Resin Technology Explained: Waterborne Forms, Performance Balance, and a Technology Map
Signal Transduction Mechanism of Graphene Biosensors: From Molecular Recognition to Electrical/Optical Signal Readout and Materials Selection
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Common Chromogenic Reagents and Method Selection for Copper Ion Content Determination
Comparison of Bilirubin Detection Methods: Application Selection of the Diazo Method, Vanadate Oxidation Method, Bilirubin Oxidase Method, and HPLC
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
Mechanism of Kojic Acid in Reducing Hyperpigmentation: From Tyrosinase Inhibition to Melanin Production Regulation
If the DNA Sequence Remains Unchanged, Why Does Gene Expression Change? Core Mechanisms and Research Methods of Epigenetic Regulation
The Skin Anti-Aging Mechanisms of α-Lipoic Acid: ALA/DHLA Redox Cycling, the Antioxidant Network, and Regulation of Collagen AGE Formation
Comparison of Iron Content Detection Methods: TPTZ, 1,10-Phenanthroline, Ferrozine, 2,2'-Bipyridine, and Instrumental Analysis
Tocopherols in the Vitamin E Family: How They Block the Chain Reaction of Lipid Peroxidation in Skin Lipids
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
The Dual-Targeted Skin-Brightening Mechanism of 4-MSK: Inhibiting Melanin Production and Reducing Epidermal Pigment Retention
Antioxidant Mechanisms, Stability, and Delivery Strategies of Resveratrol in Skincare Research
Antioxidant Mechanisms of Ferulic Acid in Skincare, Vitamin C/E Synergy, and Stable Delivery Applications
Skin Anti-Aging Mechanisms of Carnosine and Decarboxy Carnosine: Active Carbonyl Scavenging, Oxidative-Stress Buffering, and Inhibition of Collagen Glycation Cross-Linking
How Do Collagen Peptides Act on the Skin? From Surface Hydration and Percutaneous Delivery to Fibroblasts and Collagen Homeostasis
Phenylethyl Resorcinol (377): Structural Characteristics, Melanogenesis-Regulating Mechanisms, and Related Applications in Formulation Research
Anti-Photoaging Potential of Artemia Extract: UV-Induced Damage Cascades, HSP70-Related Stress Protection, and GP4G Metabolic Insights
Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications
Potential Mechanisms of Tea Polyphenols in Oily, Acne-Prone Skin: Effects of EGCG on Sebum Production, Lipid Peroxidation, and Inflammatory Responses
Mechanism of Action of Tranexamic Acid in Pigmentation Care: From the Plasmin System to Regulation of Inflammation-Driven Pro-Melanogenic Signaling
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis
What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling
Mechanisms of Retinol Action in the Skin: From Metabolic Activation and RAR/RXR-Mediated Transcriptional Regulation to Epidermal Renewal and Collagen Homeostasis
Mechanisms by Which PDRN Participates in Skin Repair: A2A Receptor-Related Signaling, Nucleotide Salvage, and Extracellular Matrix Remodeling
What Is “Plant Collagen”? Distinguishing Ingredient Types, Structural Differences, Production Methods, and Skincare Effects
How Coenzyme Q10 Acts on the Skin: Mitochondrial Electron Transfer, Antioxidant Protection of Membrane Lipids, and Lipid-Carrier Delivery
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
How Arbutin Regulates Melanin Production: α/β Anomeric Configuration and Tyrosinase Action
Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies
Structural Characteristics of Ergothioneine, OCTN1-Mediated Uptake by Skin Cells, and Antioxidant Mechanisms
Differences Between Animal-Derived Collagen and Recombinant Collagen in Skincare: Sequence and Structure, Safety, Skin Effects, and Evidence Evaluation
Regulatory Mechanisms of 5mC DNA Methylation
Structural and Functional Differences Between Idebenone and Coenzyme Q10: From Side-Chain Structure to Redox Cycling and Mitochondrial Electron Transport
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View Moligand™ grade guide → View Suitable for plant cell culture grade guide →

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.