3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctyl methacrylate - ≥98%, contains MEHQ as inhibitor , CAS No.2144-53-8

CAS: 2144-53-8 Cat. No.: T122282 Molecular Weight: 432.18 EC Number: 218-407-9
AVAILABLE TO ORDER
GRADE & PURITY ≥98% contains MEHQ as inhibitor
Synonyms
FAMAC 6 | 4(3H)-Quinazolinone, 3-(2-ethylphenyl)-2-methyl- | C12H9F13O2 | A3INR94K4A | Methacrylic Acid 1H,1H,2H,2H-Tridecafluoro-n-octyl Ester | CAPSTONE 62MA | 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctyl methacrylate | EC 218-407-9 | SCHEMBL476532 | 1h
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
T122282-5g
2
$12.90
25g
T122282-25g
3
$20.90
100g
T122282-100g
8
$65.90
500g
T122282-500g
1
$228.90
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Why this grade

≥98%, contains MEHQ as inhibitor for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
FAMAC 6 | 4(3H)-Quinazolinone, 3-(2-ethylphenyl)-2-methyl- | C12H9F13O2 | A3INR94K4A | Methacrylic Acid 1H, 1H, 2H, 2H-Tridecafluoro-n-octyl Ester | CAPSTONE 62MA | 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 8-Tridecafluorooctyl methacrylate | EC 218-407-9 | SCHEMBL476532 | 1h
Specifications & Purity
≥98%, contains MEHQ as inhibitor
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504754903
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754903
Canonical SmilesCC(=C)C(=O)OCCC(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F
IUPAC Name3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-methylprop-2-enoate
InChIKeyCDXFIRXEAJABAZ-UHFFFAOYSA-N
INCHI1S/C12H9F13O2/c1-5(2)6(26)27-4-3-7(13,14)8(15,16)9(17,18)10(19,20)11(21,22)12(23,24)25/h1,3-4H2,2H3
Isomeric SMILES CC(=C)C(=O)OCCC(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F
WGK Germany 3
RTECS UD3580000
Molecular Weight 432.18
Reaxy-Rn 6239006

Documentation

📋 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
ClassCarboxylic 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  Organofluorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl fluorides  
Molecular FrameworkAliphatic acyclic compounds
Substituents Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

26 results found

Lot NumberCertificate TypeDateItem
D2428006Certificate of AnalysisFeb 05, 2026 T122282
D2403644Certificate of AnalysisJan 19, 2026 T122282
J2515796Certificate of AnalysisSep 23, 2025 T122282
J2515728Certificate of AnalysisSep 23, 2025 T122282
D2014039Certificate of AnalysisAug 15, 2025 T122282
E2508425Certificate of AnalysisApr 27, 2025 T122282
E2508439Certificate of AnalysisApr 27, 2025 T122282
F2328875Certificate of AnalysisApr 02, 2025 T122282
F2328874Certificate of AnalysisApr 02, 2025 T122282
F2328871Certificate of AnalysisApr 02, 2025 T122282
F2328862Certificate of AnalysisApr 02, 2025 T122282
K2427791Certificate of AnalysisOct 16, 2024 T122282
K2427790Certificate of AnalysisOct 16, 2024 T122282
D2403557Certificate of AnalysisMar 21, 2024 T122282
D2416547Certificate of AnalysisMar 16, 2024 T122282
D2416543Certificate of AnalysisMar 16, 2024 T122282
K2314571Certificate of AnalysisNov 02, 2023 T122282
K2314572Certificate of AnalysisNov 02, 2023 T122282
F2328870Certificate of AnalysisJun 05, 2023 T122282
F2328873Certificate of AnalysisJun 05, 2023 T122282
F2101354Certificate of AnalysisMar 10, 2023 T122282
F2101335Certificate of AnalysisMar 10, 2023 T122282
F2101334Certificate of AnalysisMar 10, 2023 T122282
A2122101Certificate of AnalysisNov 14, 2022 T122282
G2223053Certificate of AnalysisJun 14, 2022 T122282
G2223054Certificate of AnalysisJun 14, 2022 T122282

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Chemical and Physical Properties
Refractive Index1.346
Boil Point(°C)92°C/8mmHg
Molecular Weight432.180 g/mol
XLogP35.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count15
Rotatable Bond Count9
Exact Mass432.039 Da
Monoisotopic Mass432.039 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count27
Formal Charge0
Complexity576.000
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
Citations of This Product
References
1. Kunlin Chen, Zhonghua Yuan, Sheng Dai, Jianlin Zhou, Kejing Yu.  (2023)  Preparation and performance of self-cleaning photothermal-induced self-healing flexible sensors.  COMPOSITES SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.compscitech.2023.110194]
2. Liangyun Yu, Yingzhuo Shen, Lu Chen, Qi Zhang, Xiaoya Hu, Qin Xu.  (2023)  Molecularly imprinted ultrasensitive cholesterol photoelectrochemical sensor based on perfluorinated organics functionalization and hollow carbon spheres anchored organic-inorganic perovskite.  BIOSENSORS & BIOELECTRONICS,      [PMID:37421798] [10.1016/j.bios.2023.115496]
3. Jianlin Zhou, Zhonghua Yuan, Han Liu, Weixing He, Kejing Yu, Kunlin Chen.  (2022)  Bio-inspired self-healing flexible films with pomegranate-shaped nanosphere loaded graphene for electromagnetic interference shielding and superhydrophobicity performances.  Journal of Materials Chemistry A,  10  (45): (24331-24344).  [PMID:] [10.1039/D2TA05088A]
4. Xiaowei Li, Ting Zhao, Huimin Wang, Xiaomeng Chu, Xuteng Xing, Shaojie Liu, Erjun Tang, Xiaodong Xu.  (2021)  External surfactant-free waterborne polyurethane grafted fluorine-containing acrylic copolymer with high hardness and low water absorption using chlorinated soybean oil-based urethane acrylate as polyol.  JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY,      [PMID:] [10.1080/01694243.2020.1862470]
5. Qiumeng Chen, Yahui Li, Ming Liu, Xuan Wu, Jianliang Shen, Liangliang Shen.  (2021)  Constructing helical nanowires via polymerization-induced self-assembly.  RSC Advances,  11  (15): (8986-8992).  [PMID:35423399] [10.1039/D1RA00439E]
6. Kun Li, Anjun Hu, Ruizhe Xu, Wang Xu, Borui Yang, Ting Li, Yuanjian Li, Zhi Wei Seh, Jianping Long, Shimou Chen.  (2025)  Decoupled Ion Transport via Triadic Molecular Synergy in Flame-Retardant Quasi-Solid Electrolytes for Safe Lithium Metal Batteries.  Advanced Energy Materials,      [PMID:] [10.1002/aenm.202501236]
7. Jinsong Wang, Huining Xiao, Haijiao Xie, Yang Huang, Farzad Seidi.  (2025)  Tailoring disulfide-embedded lignin-based hydrophobic self-healing coatings for metal protection.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40280525] [10.1016/j.ijbiomac.2025.143448]
8. Jin Zhang, Jianfeng Li, Dingguo Zhao, Mingjun Chen, Zhaohui Zheng, Ting Wang, Wenli An, Zhicheng Fu, Guoxing Sun, Jinni Deng.  (2026)  Chitosan aerogel composites with durable flame retardancy and prominent water resistance by one-step blending method.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41722800] [10.1016/j.ijbiomac.2026.151025]
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