Ethylacetate - UltraPureChrom™, for LC-MS, ≥99.9%(GC) , CAS No.141-78-6

CAS: 141-78-6 Cat. No.: E116141 분자식: C4H8O2 분자량: 88.11 Beilstein Registry Number: 506104 EC 번호: 205-500-4
주문 가능
등급 & 순도 UltraPureChrom™ ? UltraPureChrom™ — Aladdin's ultra-pure line for chromatography and spectroscopy. Use as a premium solvent/reagent where the lowest impurity background is required. for LC-MS ? LC-MS grade — very low metal/ion and non-volatile residues to protect mass-spec signal. Use for LC-MS where ion suppression and background must be minimal. ≥99.9%(GC)
Synonyms
Acetic acid ethyl ester | Acetidin | Vinegar naphtha | Acetic acid, ethyl ester | Essigester | Ethylacetate | EtOAc | AcOEt | 1-acetoxyethane | Acetic ether | Acetoxyethane | Ethylacetat | Aethylacetat | Acetic ester | RCRA waste number U112 | Ethyl ethan
Storage
Room temperature
Shipped In
FedEx DG Service
★
크기
USA
독일 (EU)*
가격
수량
500ml
E116141-500ml
3 재고 있음
—
US$62.90
Enter a quantity for the sizes you want to add.

개요

It has a fruity aroma, is volatile, sensitive to air, can absorb moisture, and moisture can slowly decompose it into an acidic reaction. Can be miscible with chloroform, alcohol, acetone, and ether, and soluble in water (10% ml/ml). Can dissolve certain metal salts (such as lithium chloride, cobalt chloride, zinc chloride, ferric chloride, etc.). Flammable. Vapors can form explosive mixtures with air. LD50 (rat, oral) 11.13ml/kg. It is stimulating. This product is a high-purity solvent that ensures baseline stability, minimum impurity levels, and high UV transmittance in LC-MS applications.

사양

동의어
Acetic acid ethyl ester | Acetidin | Vinegar naphtha | Acetic acid, ethyl ester | Essigester | Ethylacetate | EtOAc | AcOEt | 1-acetoxyethane | Acetic ether | Acetoxyethane | Ethylacetat | Aethylacetat | Acetic ester | RCRA waste number U112 | Ethyl ethan
사양 및 순도
UltraPureChrom™, for LC-MS, ≥99.9%(GC)
보관 조건
Room temperature
배송
FedEx DG Service
등급
for LC-MS, UltraPureChrom™
순수함
≥99.9%(GC)
이름과 식별자
Pubchem Sid
정식 스마일
CCOC(=O)C
IUPAC Name
ethyl acetate
InChIKey
XEKOWRVHYACXOJ-UHFFFAOYSA-N
INCHI
1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
이성체 SMILES
CCOC(=O)C
WGK 독일
1
RTECS
AH5425000
UN 번호
1173
포장 그룹
II
분자량
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=

고급 데이터

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
분류Carboxylic 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
설명This 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
3D 구조
상호 작용 화학 구조 모델





관련 대상(인간)
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
관련 대상(비인간)
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
작용 메커니즘
인증서(CoA, COO, BSE/TSE 및 분석 차트)
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.

47 results found

Lot NumberCertificate Type날짜항목
J2621149J2621149Certificate of AnalysisOct 12, 2026 E116141
J2621148J2621148Certificate of AnalysisOct 12, 2026 E116141
J2621147J2621147Certificate of AnalysisOct 12, 2026 E116141
J2621146J2621146Certificate of AnalysisOct 12, 2026 E116141
J2616789J2616789Certificate of AnalysisOct 12, 2026 E116141
J2615833J2615833Certificate of AnalysisOct 12, 2026 E116141
H2631261H2631261Certificate of AnalysisAug 13, 2026 E116141
H2631250H2631250Certificate of AnalysisAug 13, 2026 E116141
H2631262H2631262Certificate of AnalysisAug 13, 2026 E116141
E2607393E2607393Certificate of AnalysisApr 24, 2026 E116141
E2607376E2607376Certificate of AnalysisApr 24, 2026 E116141
E2607361E2607361Certificate of AnalysisApr 24, 2026 E116141
I2510336I2510336Certificate of AnalysisAug 27, 2025 E116141
I2510636I2510636Certificate of AnalysisAug 27, 2025 E116141
I2510641I2510641Certificate of AnalysisAug 27, 2025 E116141
E2529368E2529368Certificate of AnalysisMay 09, 2025 E116141
E2529370E2529370Certificate of AnalysisMay 09, 2025 E116141
E2529369E2529369Certificate of AnalysisMay 09, 2025 E116141
A2521369A2521369Certificate of AnalysisDec 31, 2024 E116141
A2521366A2521366Certificate of AnalysisDec 31, 2024 E116141
A2521315A2521315Certificate of AnalysisDec 31, 2024 E116141
K2405472K2405472Certificate of AnalysisOct 25, 2024 E116141
K2405473K2405473Certificate of AnalysisOct 25, 2024 E116141
K2405474K2405474Certificate of AnalysisOct 25, 2024 E116141
F2424213F2424213Certificate of AnalysisJun 13, 2024 E116141
F2424214F2424214Certificate of AnalysisJun 13, 2024 E116141
C23301055C23301055Certificate of AnalysisJan 12, 2024 E116141
A2426409A2426409Certificate of AnalysisJan 05, 2024 E116141
A2426407A2426407Certificate of AnalysisJan 05, 2024 E116141
A2426410A2426410Certificate of AnalysisJan 05, 2024 E116141
A2426411A2426411Certificate of AnalysisJan 05, 2024 E116141
G2315687G2315687Certificate of AnalysisJul 01, 2023 E116141
G2315679G2315679Certificate of AnalysisJul 01, 2023 E116141
G2315692G2315692Certificate of AnalysisJul 01, 2023 E116141
E23061007E23061007Certificate of AnalysisMar 22, 2023 E116141
C2330143C2330143Certificate of AnalysisMar 06, 2023 E116141
C2330105C2330105Certificate of AnalysisMar 06, 2023 E116141
B2310147B2310147Certificate of AnalysisDec 09, 2022 E116141
B2310149B2310149Certificate of AnalysisDec 09, 2022 E116141
B2310199B2310199Certificate of AnalysisDec 09, 2022 E116141
J2225605J2225605Certificate of AnalysisOct 09, 2022 E116141
J2225572J2225572Certificate of AnalysisOct 09, 2022 E116141
J2225571J2225571Certificate of AnalysisOct 09, 2022 E116141
I2203204I2203204Certificate of AnalysisAug 19, 2022 E116141
I2203198I2203198Certificate of AnalysisAug 19, 2022 E116141
I2203197I2203197Certificate of AnalysisAug 19, 2022 E116141
G2131206G2131206Certificate of AnalysisMay 09, 2022 E116141
화학 및 물리적 특성
굴절률1.3720
발화점(°C)-3°C
끓는점(°C)76.5-77.5 °C
녹는점(°C)-84 °C
분자량88.110 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
자주 묻는 질문과 기사
UltraPureChrom™: The Pinnacle of Purity for Chromatography
LC-MS Grade Solvents and Reagents
A New Esterification Method — Rapid Esterification Mediated by the Coupling Reagent NDTP
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
Calcium Gluconate: Physicochemical Properties, Pharmacopoeial Quality Control, and Application Guidelines
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
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
Experimental Judgment in Oxyma Coupling Systems: Coupling Efficiency, Racemization Control, and the HCN Risk in DIC-Based Systems
Preparation Methods and Precautions for Silane Coupling Agent Primer Solutions
Key Control Points in Polyurethane Coating Formulation Design and Application
Silicone Resin Coating Formulation Design: From Application Conditions to Matching Resins, Pigments and Fillers, Curing, and Substrates
VC/VAc Resins and Their Modification: An Analysis of VC/VAc Vinyl Resins for Coatings and Inks
Formulation Design of Chlorinated Rubber Coatings: Component Synergy and Performance Control
How to Select Vinyl-Related Resins: Building Formulation Judgment Based on Substrate, Performance Targets, and Failure Risks
What Is Chlorinated Rubber Resin? An Analysis of Structural Characteristics, Chlorination Modification, and Coating Film-Formation Mechanisms
Applicability Boundaries, Failure Risks, and Alternative System Selection for Chlorinated Rubber Resin in Coatings
The Chemical Basis of Natural Lacquer Durability: Urushiol Structure, Oxidative Polymerization Film Formation, and Coating Film Properties
Guide to Traditional Natural Varnish Resins: Transparency, Gloss, Film Formation, Aging, and Application Selection of Dammar, Mastic, and Copal
Mechanism, Diagnosis, and Control of Coating Lifting: Solvent Penetration, Film Swelling, and Interlayer Instability
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
Solvents, Co-solvents, and Solubilization Systems in Home and Personal Care Formulations: Classification, Functions, and Selection Guide
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Discovery and Structural Optimization of the Noncovalent 3CL Protease Inhibitor S-217622
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
Stereoretentive Decarboxylative Amidation with Dioxazolones: A Two-Electron Rearrangement Mechanism for Stereochemical Transfer from Chiral Carboxylic Acids
Construction of the Key α-Bromoketone Intermediate for LY3509754: A β-Keto Ester Strategy and Concomitant Decarboxylation Following Enzymatic Ester Hydrolysis
How to Evaluate Reaction Generality through Substrate Scope: From the Number of Examples to Standardized Substrate Selection
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
Citations of This Product
솔루션 계산기
리뷰

고객 리뷰

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.