6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate
C16H23NO4
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Identification
- CAS Number
- 63740-41-0
- EC Number
- 404-870-6
- UN Number
- 3082
- Index Number
- 607-222-00-2
- PubChem CID
- 5463785
Physical-chemical properties
- Molecular Formula
- C16H23NO4
- Molar Mass
- 293.36 g/mol
- IUPAC Name
- 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate
Chemical Identifiers
- InChI
- InChI=1S/C16H23NO4/c1-11(2)16(20)21-10-8-6-5-7-9-17-14(18)12(3)13(4)15(17)19/h1,5-10H2,2-4H3
- InChI Key
- SGONPVYGYALKRZ-UHFFFAOYSA-N
Overview
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate (CAS 63740-41-0) is a specialized maleimide-functionalized methacrylate monomer with dual reactive functionality for advanced polymer synthesis. This technical-grade chemical compound combines the reactivity of both maleimide and methacrylate functional groups within a single molecular structure, making it particularly valuable for creating crosslinked polymer networks and functionalized materials. With a molecular formula of C16H23NO4 and molecular weight of 293.36 g/mol, this bifunctional monomer enables precise control over polymer architecture and properties. The compound features a hexyl spacer chain connecting the maleimide ring system to the methacrylate group, providing flexibility for various polymerization strategies. From a safety perspective, this substance is classified as Skin Sens. 1 under GHS regulations, indicating potential for skin sensitization, and carries Aquatic Chronic 2 classification for environmental considerations. The compound displays GHS07 and GHS09 pictograms with a "Warning" signal word, requiring appropriate handling protocols including personal protective equipment and controlled storage conditions. Its ADR Class 9 designation classifies it as a miscellaneous dangerous substance for transport purposes. Primary industrial applications include specialty adhesive formulations, biomedical polymer synthesis, and advanced composite materials where controlled crosslinking is essential. The maleimide functionality enables specific protein conjugation reactions, while the methacrylate group participates in free radical polymerization processes. Unlike simpler compounds such as ethyl 6,8-dichlorooctanoate, this bifunctional monomer offers enhanced design flexibility for sophisticated material engineering applications. OYSI maintains reliable European supply chains for this specialized monomer, supporting customers across polymer science, materials engineering, and specialty chemical manufacturing sectors.
Safety & Classification
Skin Sens. 1; Aquatic Chronic 2
GHS Pictograms
HHazard Statements (H-Statements)
Describe the nature and severity of the hazard
Classification according to CLP Regulation (EC) No 1272/2008. The complete list of hazard and precautionary statements can be found in the Safety Data Sheet (SDS).
First Aid Measures
Skin Contact
Measures if substance contacts the skin
First Aid Actions
- +P302IF ON SKIN:
- +P352Wash with plenty of water.
- +P361Take off immediately all contaminated clothing.
- +P313Get medical advice/attention.
Related hazard statements:
General Measures
Emergency 112 | Poison Control: +49 30 19240 (DE), +33 1 45 42 59 59 (FR), +31 30 274 88 88 (NL)
First aid measures are based on CLP classification and associated P-statements. They do not replace the Safety Data Sheet (SDS). In case of emergency, always consult the full SDS and a physician.
Transport (ADR)
| UN Number | 3082 |
| ADR Class | 9 |
| Packing Group | III |
| Tunnel Code | - |
| Proper Shipping Name | 6-(2,3-Dimethylmaleimido)hexylmethacrylat |
| Marine Pollutant | No |
Frequently Asked Questions
What is 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is a specialized organic compound with the molecular formula C16H23NO4 and CAS number 63740-41-0. This substance has a molecular weight of 293.36 g/mol and features a complex structure combining a pyrrol ring system with a methacrylate ester group. It is classified as a skin sensitizer and poses chronic aquatic toxicity concerns, requiring careful handling in industrial applications.
What are the physicochemical properties of 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is an organic compound with a molecular weight of 293.36 g/mol and molecular formula C16H23NO4. As a methacrylate ester derivative, it likely exists as a liquid at room temperature with moderate volatility. The compound contains both hydrophilic and lipophilic portions, suggesting intermediate solubility characteristics. Specific physical properties such as boiling point, density, and exact solubility parameters would require detailed technical documentation.
What is 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate used for?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is primarily used as a specialized monomer in polymer chemistry and materials science applications. The methacrylate functionality enables polymerization reactions, while the pyrrol ring system provides unique chemical properties. It is typically employed in the synthesis of functional polymers, specialty coatings, or advanced materials where specific chemical reactivity or biocompatibility is required. Professional use is recommended due to its sensitizing properties.
How to handle 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate safely?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate requires careful handling due to its skin sensitizing properties (Skin Sens. 1). Mandatory personal protective equipment includes chemical-resistant gloves, safety glasses, and protective clothing to prevent skin contact. Work in well-ventilated areas or under fume hoods to minimize inhalation exposure. Avoid direct skin and eye contact, and ensure emergency eyewash stations and safety showers are readily accessible during handling operations.
How to store 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate correctly?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate should be stored in tightly sealed containers in a cool, dry, and well-ventilated area away from heat sources and direct sunlight. As a methacrylate compound, it may require stabilizers to prevent unwanted polymerization during storage. Keep containers upright and properly labeled, and store away from incompatible materials such as strong oxidizers. Regular temperature monitoring and inventory rotation following FIFO principles are recommended for optimal product stability.
What to do in case of contact with 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate?
Immediate action is required for any contact with 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate due to its sensitizing properties. For skin contact, immediately remove contaminated clothing and wash affected areas thoroughly with soap and water for at least 15 minutes. In case of eye contact, flush with clean water for 15 minutes while holding eyelids open. If inhaled, move to fresh air immediately. Seek medical attention if irritation develops or persists, and inform medical personnel of the substance's sensitizing nature.
How to dispose of 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate appropriately?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate must be disposed of through licensed hazardous waste contractors in accordance with local and European waste regulations. The substance cannot be disposed of in regular waste streams due to its hazardous classification and environmental concerns (Aquatic Chronic 2). Waste containers must be properly labeled and documented for traceability. Small quantities may require special incineration at high temperatures in approved facilities to ensure complete destruction while preventing environmental contamination.
How to transport 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is classified as ADR Class 9 (Miscellaneous Dangerous Goods), Packing Group III for transportation purposes. This classification requires appropriate packaging, labeling with Class 9 hazard labels, and proper shipping documentation including transport documents and emergency response information. The substance must be transported by qualified carriers familiar with hazardous materials regulations. Packaging must meet UN specification standards and be compatible with the chemical properties of the substance.
Is 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate subject to specific regulations?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is subject to European REACH and CLP regulations due to its hazardous classification. The substance is classified as Skin Sens. 1 and Aquatic Chronic 2, requiring appropriate safety data sheets and hazard communication. It is not currently identified as a Substance of Very High Concern (SVHC). Companies using this substance must comply with registration requirements, exposure assessment obligations, and implement appropriate risk management measures according to REACH provisions.
Where to buy 6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate in Europe?
6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is available through OYSI, a specialized European distributor of technical chemical products. OYSI provides professional-grade chemicals with proper documentation, including safety data sheets and certificates of analysis. As an established European chemical distributor, OYSI ensures compliance with REACH and CLP regulations, offering reliable supply chain solutions for industrial and research applications. Contact OYSI directly for availability, technical specifications, and customized packaging options for your specific requirements.
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6-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)hexyl 2-methylprop-2-enoate is a dangerous good. We support you with labeling, packaging, and transport documentation.
Data Sources
Classification per CLP Regulation (EC) No 1272/2008. Data from ECHA and PubChem.