Edrophonium Chloride - ≥98% , Acetylcholinesterase inhibitor, CAS No.116-38-1, Acetylcholinesterase inhibitor

CAS: 116-38-1 Cat. No.: E131855 Formule: C10H16ClNO Poids moléculaire: 201.69 Numéro CE: 204-138-4
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%
Synonyms
Edrophonium chloride (USP:INN:BAN:JAN) | SR-01000000275 | Cloruro de edrofonio (INN-Spanish) | SR-01000000275-4 | FT-0657849 | MFCD00055064 | NCGC00093908-03 | DS-0552 | EDROPHONIUM CHLORIDE [USP-RS] | EU-0100511 | NCGC00261196-01 | AKOS015890417 | Ethyl(
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Allemagne (EU)
USA*
Price
Qty
50mg
E131855-50mg
—
2 En stock

12,06€

18,14€
Enregistrer 6,07 € (33.49%)
250mg
E131855-250mg
—
1 En stock

45,04€

67,60€
Enregistrer 22,56 € (33.38%)
1g
E131855-1g
Sur commande · 8–12 semaines

116,19€

174,33€
Enregistrer 58,14 € (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Edrophonium chloride is a readily reversible acetylcholinesterase inhibitor; prevents breakdown of the neurotransmitter acetylcholine and acts by competitively inhibiting the enzyme acetylcholinesterase, mainly at the neuromuscular junction.

Specifications

Synonymes
Edrophonium chloride (USP:INN:BAN:JAN) | SR-01000000275 | Cloruro de edrofonio (INN-Spanish) | SR-01000000275-4 | FT-0657849 | MFCD00055064 | NCGC00093908-03 | DS-0552 | EDROPHONIUM CHLORIDE [USP-RS] | EU-0100511 | NCGC00261196-01 | AKOS015890417 | Ethyl(
Spécifications et pureté
≥98%
Conditions de stockage de stockage
Protected from light,Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Type d'action
INHIBITOR
Mécanisme d'action
Acetylcholinesterase inhibitor
Pureté
≥98%
Noms et identifiants
Pubchem Sid504751643
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751643
Sourires canoniquesCC[N+](C)(C)C1=CC(=CC=C1)O.[Cl-]
IUPAC Nameethyl-(3-hydroxyphenyl)-dimethylazanium;chloride
InChIKeyBXKDSDJJOVIHMX-UHFFFAOYSA-N
INCHI1S/C10H15NO.ClH/c1-4-11(2,3)9-6-5-7-10(12)8-9;/h5-8H,4H2,1-3H3;1H
Isomères SMILES CC[N+](C)(C)C1=CC(=CC=C1)O.[Cl-]
CAS alternatif 312-48-1;302-83-0
Poids moléculaire 201.69
Reaxy-Rn 3748734
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3748734&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
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassAniline and substituted anilines
Intermediate Tree Nodes Not available
Direct ParentAniline and substituted anilines
Alternative Parents m-Aminophenols  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Quaternary ammonium salts  Organopnictogen compounds  Organooxygen compounds  Organic chloride salts  Hydrocarbon derivatives  Amines  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aminophenol - M-aminophenol - Aniline or substituted anilines - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Quaternary ammonium salt - Amine - Organic chloride salt - Hydrocarbon derivative - Organic salt - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors chloride salt - quaternary ammonium salt
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
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SMN1 Tchem Survival motor neuron protein (34246 Activities)
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BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Cholinesterases; ACHE & BCHE (1222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay 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.

5 results found

Lot NumberCertificate TypeDateArticle
G2403531Certificate of AnalysisApr 03, 2026 E131855
G2027134Certificate of AnalysisMay 09, 2024 E131855
B2422032Certificate of AnalysisMar 04, 2024 E131855
G2027133Certificate of AnalysisFeb 20, 2024 E131855
G2027135Certificate of AnalysisFeb 20, 2024 E131855
Propriétés chimiques et physiques
SensibilitéMoisture sensitive. Light sensitive.
Poids moléculaire201.690 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass201.092 Da
Monoisotopic Mass201.092 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count13
Formal Charge0
Complexity145.000
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 Count2
Calculateurs de solution
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