Butyl methacrylate - Standard for GC, ≥99.5%(GC), Containing MEHQ stabilizer , CAS No.97-88-1

CAS: 97-88-1 Cat. No.: B110904 Formula: C8H14O2 Peso molecolare: 142.2 Beilstein Registry Number: 773960 Numero EC: 202-615-1
Disponibile su ordine
GRADE & PURITY Standard for GC ? GC reference standard — characterized compound for calibrating GC methods. Use to build calibration curves and verify GC quantitation. ≥99.5%(GC) Containing MEHQ stabilizer
Synonyms
Butil metacrilato [Italian] | Butyl ester of methacrylic acid | EC 202-615-1 | nBMA | Butylester kyseliny methakrylove | DTXSID4024696 | NSC20956 | 2-Methyl-butylacrylat | 2-Propenoic acid, 2-methyl-, butyl ester | DTXCID704696 | n-butylmethacrylate | STL
Storage
Room temperature
Shipped In
FedEx DG Service
★
Size
Germania (EU)
USA*
Price
Qty
5ml
B110904-5ml
Disponibile ≥10
Disponibile ≥10
12,93€
25ml
B110904-25ml
—
5 Disponibile
43,30€
50ml
B110904-50ml
—
5 Disponibile
60,65€
Enter a quantity for the sizes you want to add.
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Why this grade

Standard for GC, ≥99.5%(GC), Containing MEHQ stabilizer Standard for GC for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships FedEx DG Service 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 96 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
Butil metacrilato [Italian] | Butyl ester of methacrylic acid | EC 202-615-1 | nBMA | Butylester kyseliny methakrylove | DTXSID4024696 | NSC20956 | 2-Methyl-butylacrylat | 2-Propenoic acid, 2-methyl-, butyl ester | DTXCID704696 | n-butylmethacrylate | STL
Specifiche e purezza
Standard for GC, ≥99.5%(GC), Containing MEHQ stabilizer
Condizioni di conservazione di stoccaggio
Room temperature
Spedito in
FedEx DG Service
Grado
Standard for GC
Purezza
≥99.5%(GC)
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508814849
Sorrisi canonici
CCCCOC(=O)C(=C)C
IUPAC Name
butyl 2-methylprop-2-enoate
InChIKey
SOGAXMICEFXMKE-UHFFFAOYSA-N
INCHI
1S/C8H14O2/c1-4-5-6-10-8(9)7(2)3/h2,4-6H2,1,3H3
Isomeri SMILES
CCCCOC(=O)C(=C)C
WGK Germania
1
RTECS
OZ3675000
Numero UN
2227
Gruppo di imballaggio
III
Peso molecolare
142.2
Beilstein
773960
Reaxy-Rn
773960
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773960&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
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters
Direct ParentEnoate esters
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





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.

8 results found

Lot NumberCertificate TypeDataOggetto
G1712091Certificate of AnalysisAug 13, 2026 B110904
B2310449Certificate of AnalysisJul 30, 2026 B110904
F2413050Certificate of AnalysisMar 09, 2026 B110904
F2413051Certificate of AnalysisMar 09, 2026 B110904
F2413052Certificate of AnalysisMar 09, 2026 B110904
E1921182Certificate of AnalysisJan 25, 2023 B110904
B2311001Certificate of AnalysisDec 06, 2022 B110904
B2311029Certificate of AnalysisDec 06, 2022 B110904
Proprietà chimiche e fisiche
Indice di rifrazione1.4229
Punto di infiammabilità (°F)129.2 °F
Punto di infiammabilità (°C)41℃
Punto di ebollizione (°C)160-163°C
Punto di fusione (°C)-75°C
Peso molecolare142.200 g/mol
XLogP32.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Exact Mass142.099 Da
Monoisotopic Mass142.099 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count10
Formal Charge0
Complexity127.000
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
Domande frequenti e articoli
Standard for GC: A Practical Guide
Structural and Performance Design of Acrylic Resins for Coatings: Monomer Composition, Key Parameters, and Film Formation/Curing Mechanisms
When Should You Choose Silicone Resin? Selection Comparison with Epoxy, Acrylic, Polyurethane, Fluororesin, and Other Coating Resins
Vinyl Acetate-Acrylic Emulsion (Vinyl Acrylic Emulsion): A Cost-Performance Balance Solution for Architectural Coatings
From Water to Film: Film-Formation Mechanisms and Performance Development of Waterborne Emulsions and Dispersions
Diagnosis of Coating Performance Issues and Selection of Resin Modification Routes
Structural Design Logic of Common Resin Modification Technologies: Molecular Chain Structure, Functional Groups, Phase Structure, Crosslinked Networks, and Hybrid/Functional Design
Citations of This Product
Calcolatori di soluzioni
Recensioni

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