Isobutyl methacrylate - ≥99%, contains MEHQ as stabilizer , CAS No.97-86-9

CAS: 97-86-9 Cat. No.: I106679 Summenformel: C₈H₁₄O₂ Molekulargewicht: 142.2 Beilstein Registry Number: 1747595 EG-Nummer: 202-613-0

GRADE & PURITY ≥99%, contains MEHQ as stabilizer

Synonyms

ISOBUTYL METHACRYLATE [INCI] | DTXSID3025461 | EINECS 202-613-0 | NCGC00259117-01 | Isobutyl 2-methylacrylate # | 2-methylpropyl 2-methylprop-2-enoate | MFCD00084435 | AKOS005622614 | Isobutylmethacrylate | NCGC00091087-01 | M0132 | MFCD00008931 | CAS-97-

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Specifications

Synonyme

ISOBUTYL METHACRYLATE [INCI] | DTXSID3025461 | EINECS 202-613-0 | NCGC00259117-01 | Isobutyl 2-methylacrylate # | 2-methylpropyl 2-methylprop-2-enoate | MFCD00084435 | AKOS005622614 | Isobutylmethacrylate | NCGC00091087-01 | M0132 | MFCD00008931 | CAS-97-

Spezifikationen & Reinheit

≥99%, contains MEHQ as stabilizer

Storage

Store at 2-8°C

Verschickt in

Wet ice,FedEx DG Service

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥99%

Namen und Kennungen

• Pubchem Sid: 508814858
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508814858
• Kanonisches Lächeln: CC(C)COC(=O)C(=C)C
• IUPAC Name: 2-methylpropyl 2-methylprop-2-enoate
• InChIKey: RUMACXVDVNRZJZ-UHFFFAOYSA-N
• INCHI: 1S/C8H14O2/c1-6(2)5-10-8(9)7(3)4/h6H,3,5H2,1-2,4H3
• Isomere SMILES: CC(C)COC(=O)C(=C)C
• WGK Deutschland: 1
• RTECS: OZ4900000
• UN-Nummer: 2283
• Verpackungsgruppe: III
• Molekulargewicht: 142.2
• Beilstein: 1747595
• Reaxy-Rn: 1747595
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1747595&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Ebene5 Carboxylic acid esters
          • Ebene6 Alpha,beta-unsaturated carboxylic esters
            • Ebene7 Enoate esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters
• Direct Parent: Enoate esters
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Solubility in water: Practically insoluble; Miscible with Ether,Ethanol
• Brechungsindex: 1.4199
• Flammpunkt (°F): 107.6 °F
• Flammpunkt (°C): 49℃
• Siedepunkt (°C): 155°C
• Schmelzpunkt (°C): -37°C
• Molekulargewicht: 142.200 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 142.099 Da
• Monoisotopic Mass: 142.099 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 136.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referenzen

1. Weixing Xu, Jianfei Zhou, Ya’nan Wang, Bi Shi.  (2016)  Modification of Leather Split by In Situ Polymerization of Acrylates.  International Journal of Polymer Science,      [PMID:] [10.1155/2016/7460572]

2. Wen Jie, Lyu Yanjun, Zhang Lianhong, Ma Yuling, Huang Xia, Zhu Wanyu.  (2024)  β-Cyclodextrin-Grafted Cobalt-Aluminum Bimetallic Oxide Modified Acrylic Ester Resin for Oil/Water Separation.  KOREAN JOURNAL OF CHEMICAL ENGINEERING,      [PMID:] [10.1007/s11814-024-00208-z]

3. Huizhu Li, Chengyang Liu, Li Zhang, Jianbo Tan.  (2025)  High-Temperature Photoinitiated RAFT Dispersion Polymerization: A Light-Mediated Approach for Controlled Synthesis of Well-Defined Polymeric Microspheres.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c03661]