🌎 Livrer à: United States
Basculer la navigation
Panier
Rechercher
Expédition le jour même pour tous les articles en stock.
Recherche Avancée
Commande rapide SDS / CoA Structure En vrac et personnalisé
Menu
Compte
Paramètres
྾
340,000+ produits de recherche · Triple ISO certified · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock

Ethylacetate - PureSpectra™, ACS, Spectrum pure, ≥99.5% , CAS No.141-78-6

CAS: 141-78-6 Cat. No.: E116137 Formule: C4H8O2 Poids moléculaire: 88.11 Beilstein Registry Number: 506104 Numéro CE: 205-500-4
1847 Citations COA
Ethylacetate - PureSpectra™, ACS, Spectrum pure, ≥99.5% CAS No(141-78-6) by Aladdin Scientific
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ PureSpectra™ ? PureSpectra™ — Aladdin's premium line for spectroscopy applications. Use where low spectral background ensures clean UV/Vis/IR measurements. ACS ? ACS grade — meets American Chemical Society specifications, the analytical benchmark in the US. Use for analytical and QC work needing ACS-defined purity. Spectrum pure ? Spectrum-pure grade with impurities controlled to a spectroscopically clean baseline. Use for spectroscopy where background signals must be minimal. ≥99.5%
Synonyms
ethyl aceate | ETHYL ACETATE [FCC] | Ethyle(acetate d') | acetic acid ethyl | acetic ethyl ester | DTXSID1022001 | Etile (acetato di) [Italian] | ETHYL ACETATE (EP MONOGRAPH) | Ethyl acetate (natural) | CH3COOC2H5 | ethy acetate | Ethyl acetate [NF] | ETH
Storage
Room temperature
Shipped In
FedEx DG Service
★
Taille
Allemagne (EU)
USA*
Prix
Qté
250ml
E116137-250ml
—
5 En stock
24,21€
500ml
E116137-500ml
—
3 En stock

31,15€

36,36€
Enregistrer 5,21 € (14.32%)
Enter a quantity for the sizes you want to add.
Vrac / Sur mesure
♡ Ajouter à ma liste d’envie ⇅ Ajouter au comparateur ⎙ Imprimer la page
SDS
Safety data
COA
Certificate
DS
Fiche technique
SP
Fiche de spécifications
Spécifications Noms et identifiants Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

Spécifications

Synonymes
ethyl aceate | ETHYL ACETATE [FCC] | Ethyle(acetate d') | acetic acid ethyl | acetic ethyl ester | DTXSID1022001 | Etile (acetato di) [Italian] | ETHYL ACETATE (EP MONOGRAPH) | Ethyl acetate (natural) | CH3COOC2H5 | ethy acetate | Ethyl acetate [NF] | ETH
Spécifications et pureté
PureSpectra™, ACS, Spectrum pure, ≥99.5%
Conditions de stockage de stockage
Room temperature
Expédié en
FedEx DG Service
Grade
ACS, PureSpectra™, Spectrum pure
Pureté
≥99.5%
Noms et identifiants
Pubchem Sid
508811903
Sourires canoniques
CCOC(=O)C
IUPAC Name
ethyl acetate
InChIKey
XEKOWRVHYACXOJ-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
Isomères SMILES
CCOC(=O)C
WGK Allemagne
1
RTECS
AH5425000
Numéro ONU
1173
Groupe d'emballage
II
Poids moléculaire
88.11
Beilstein
506104
Reaxy-Rn
506104
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506104&ln=

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acid esters
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
External Descriptors a small molecule
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTSB Tchem Cathepsin B (3822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KG-1 (867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Cruzipain (33337 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTSL Cathepsin L (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vibrio parahaemolyticus (473 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Listeria monocytogenes (2626 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus cereus (7522 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryctolagus cuniculus (11301 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.

13 results found

Lot NumberCertificate TypeDateArticle
K2208341K2208341Certificate of AnalysisAug 03, 2026 E116137
F2526028F2526028Certificate of AnalysisJul 04, 2025 E116137
F2526031F2526031Certificate of AnalysisJun 30, 2025 E116137
J2421320J2421320Certificate of AnalysisOct 26, 2024 E116137
J2421321J2421321Certificate of AnalysisOct 26, 2024 E116137
L2311222L2311222Certificate of AnalysisJan 04, 2024 E116137
L2311224L2311224Certificate of AnalysisDec 18, 2023 E116137
L2205445L2205445Certificate of AnalysisDec 08, 2022 E116137
B2210400B2210400Certificate of AnalysisFeb 14, 2022 E116137
B2210484B2210484Certificate of AnalysisFeb 14, 2022 E116137
F2221038F2221038Certificate of AnalysisFeb 14, 2022 E116137
F2221046F2221046Certificate of AnalysisDec 06, 2021 E116137
K2129626K2129626Certificate of AnalysisDec 06, 2021 E116137
Propriétés chimiques et physiques
SolubilitéSlightly soluble in water; Miscible with Chloroform; Soluble in Ether,Benzene,Acetone,Alcohol
Indice de réfraction1.3720
Point d'éclair (°C)-3°C
Point d'ébullition (°C)76.5-77.5 °C
Point de fusion (°C)-84 °C
Poids moléculaire88.110 g/mol
XLogP30.700
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass88.0524 Da
Monoisotopic Mass88.0524 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity49.500
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
FAQ et articles
PureSpectra™: Premium Quality for Spectroscopy Applications
Categories: Reagent Specifications, Grading and Purity
Tags:
Specification Purity Grade PureSpectra for spectroscopy
What is Spectrum Pure Grade? A Complete Guide
Categories: Reagent Specifications, Grading and Purity
Tags:
Spectrum pure
A New Esterification Method — Rapid Esterification Mediated by the Coupling Reagent NDTP
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Esterification Method
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
TEMPO
Calcium Gluconate: Physicochemical Properties, Pharmacopoeial Quality Control, and Application Guidelines
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Calcium Ion Quality control calcium gluconate D-gluconic acid hyperkalemia hydrofluoric acid exposure soy-product coagulation pharmacopeial standards
Chlorophyll: Structural Features, Physicochemical Properties, and Key Points for Research and Industrial Applications
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
stability HPLC Fluorescence Magnesium chlorophyll chlorophyll a chlorophyll b porphyrin ring phytol pheophytin Cu/Zn complexes
Ferulic Acid: Structural Features, Preparation Routes, and Key Points for Research Applications
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
ferulic acid 3-methoxy-4-hydroxycinnamic acid
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
AAAs β-Acyloxy Alkenyl Amides
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
DSC N,N′-disuccinimidyl carbonate
Experimental Judgment in Oxyma Coupling Systems: Coupling Efficiency, Racemization Control, and the HCN Risk in DIC-Based Systems
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Coupling Oxyma Coupling Systems Oxyma ethyl 2-cyano-2-(hydroxyimino)acetate OxymaPure
Preparation Methods and Precautions for Silane Coupling Agent Primer Solutions
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Silane Coupling Agent Primer Solutions
Key Control Points in Polyurethane Coating Formulation Design and Application
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Polyurethane Polyurethane Coatings
Silicone Resin Coating Formulation Design: From Application Conditions to Matching Resins, Pigments and Fillers, Curing, and Substrates
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Silicone Resins Silicone Resin Coating
VC/VAc Resins and Their Modification: An Analysis of VC/VAc Vinyl Resins for Coatings and Inks
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Ink thermoplastic resin VC/VAc resins Paint
Formulation Design of Chlorinated Rubber Coatings: Component Synergy and Performance Control
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
resin Paint Film-forming resin Chlorinated Rubber Coatings
How to Select Vinyl-Related Resins: Building Formulation Judgment Based on Substrate, Performance Targets, and Failure Risks
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
resin Paint
What Is Chlorinated Rubber Resin? An Analysis of Structural Characteristics, Chlorination Modification, and Coating Film-Formation Mechanisms
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Ink resin Paint Adhesive Chlorine containing film-forming resin
Applicability Boundaries, Failure Risks, and Alternative System Selection for Chlorinated Rubber Resin in Coatings
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
resin Paint Chlorinated rubber resin
The Chemical Basis of Natural Lacquer Durability: Urushiol Structure, Oxidative Polymerization Film Formation, and Coating Film Properties
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Coating Material Natural Paint
Guide to Traditional Natural Varnish Resins: Transparency, Gloss, Film Formation, Aging, and Application Selection of Dammar, Mastic, and Copal
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Natural resin Coating Material
Mechanism, Diagnosis, and Control of Coating Lifting: Solvent Penetration, Film Swelling, and Interlayer Instability
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Paint Paint biting bottom
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
resin Paint formulation Resin polarity
Solvents, Co-solvents, and Solubilization Systems in Home and Personal Care Formulations: Classification, Functions, and Selection Guide
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Solvents Co-solvents
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Peptide synthesis coupling reagent coupling reagents
Discovery and Structural Optimization of the Noncovalent 3CL Protease Inhibitor S-217622
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
3C-like protease main protease
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines
Stereoretentive Decarboxylative Amidation with Dioxazolones: A Two-Electron Rearrangement Mechanism for Stereochemical Transfer from Chiral Carboxylic Acids
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Dioxazolone Decarboxylative Amidation Decarboxylation coupling
Categories:
Tags:
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Categories:
Tags:
Categories:
Tags:
Categories:
Tags:
How to Evaluate Reaction Generality through Substrate Scope: From the Number of Examples to Standardized Substrate Selection
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
substrate scope
Bond-Formation Sequence and Process Improvement for 3-Bromo-6-alkyl-1,6-naphthyridin-5(6H)-ones: From Late-Stage N-Alkylation to Enamine Cyclization with Primary Amines
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Enamine cyclization 3-bromo-N-alkyl-1,6-naphthyridones
Citations of This Product
How to Cite Aladdin Scientific Products? Citations Search
Calculateurs de solution
Avis

Avis des clients

Nous utilisons des cookies pour garantir le bon fonctionnement du site et, lorsque cela est autorisé, pour améliorer votre expérience. Vous pouvez gérer vos préférences à tout moment dans les Paramètres. Pour en savoir plus, consultez notre Politique relative aux cookies.

Souhaitez-vous que nous vous envoyions un message lorsque des réductions seront disponibles?

Me rappeler plus tard

Merci ! Veuillez vérifier votre boîte de réception e-mail pour confirmer.

Oups ! Les notifications sont désactivées.

Privacy Policy Terms of Use Cookie Policy Terms and Conditions of Sale Sales Policy
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corporation. All rights reserved.