3-Methylthiophene - ≥98% , CAS No.616-44-4

CAS: 616-44-4 Cat. No.: M113676 Peso molecular: 98.17 Beilstein Registry Number: 1300 Número EC: 210-482-6
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
beta-Methylthiophene | FT-0616025 | 3-THIENYLMETHANE | EN300-55387 | NSC65439 | NSC-65439 | Q-100711 | 3-Methylthiophene, 98% | 3-Methylthiophene, analytical standard | BRN 0001300 | Methyl-3-thiophene | PS-9336 | Thiophene, 3-methyl- | DTXSID8060666 | CC
Storage
Room temperature
Shipped In
FedEx DG Service
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
M113676-5g
2
9,90US$
5ml
M113676-5ml
9
9,90US$
25ml
M113676-25ml
8
19,90US$
100ml
M113676-100ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
55,90US$
500ml
M113676-500ml
3
189,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships FedEx DG Service 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 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Conducting polymer precursor

Specifications

Sinónimos
beta-Methylthiophene | FT-0616025 | 3-THIENYLMETHANE | EN300-55387 | NSC65439 | NSC-65439 | Q-100711 | 3-Methylthiophene, 98% | 3-Methylthiophene, analytical standard | BRN 0001300 | Methyl-3-thiophene | PS-9336 | Thiophene, 3-methyl- | DTXSID8060666 | CC
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
FedEx DG Service
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488181514
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181514
Sonrisas canónicasCC1=CSC=C1
IUPAC Name3-methylthiophene
InChIKeyQENGPZGAWFQWCZ-UHFFFAOYSA-N
INCHI1S/C5H6S/c1-5-2-3-6-4-5/h2-4H,1H3
Isómeros SMILES CC1=CSC=C1
WGK Alemania 3
RTECS XM9800000
Número ONU 1993
Peso molecular 98.17
Beilstein 1300
Reaxy-Rn 1300
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1300&ln=

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
SuperclassOrganoheterocyclic compounds
ClaseHeteroaromatic compounds
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentHeteroaromatic compounds
Alternative Parents Thiophenes  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Heteroaromatic compound - Thiophene - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

13 results found

Lot NumberCertificate TypeFechaArticulo
D2620014Certificate of AnalysisApr 29, 2026 M113676
K1913103Certificate of AnalysisApr 10, 2024 M113676
B2627197Certificate of AnalysisSep 28, 2022 M113676
D2319384Certificate of AnalysisSep 28, 2022 M113676
D2319394Certificate of AnalysisSep 28, 2022 M113676
D2501037Certificate of AnalysisSep 28, 2022 M113676
D2521003Certificate of AnalysisSep 28, 2022 M113676
H2513089Certificate of AnalysisSep 28, 2022 M113676
L2201318Certificate of AnalysisSep 28, 2022 M113676
L2201373Certificate of AnalysisSep 28, 2022 M113676
L2201402Certificate of AnalysisSep 28, 2022 M113676
L2201827Certificate of AnalysisSep 28, 2022 M113676
C2201059Certificate of AnalysisMar 29, 2022 M113676

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Propiedades químicas y físicas
SolubilidadSoluble in water (0.4 mg/ml at 25 °C), ethanol, ether, acetone, and benzene.
Índice de refracción1.518-1.52
Punto de inflamación (°F)53.6 °F
Punto de inflamación (°C)11℃
Punto de ebullición (°C)114°C
Punto de fusión (°C)-69°C
Peso molecular98.170 g/mol
XLogP32.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass98.019 Da
Monoisotopic Mass98.019 Da
Topological Polar Surface Area28.200 Ų
Heavy Atom Count6
Formal Charge0
Complexity43.200
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
Referencias
1. Wen Wang, Jie Cao, Jiawen Yu, Fajuan Tian, Xiaoyu Luo, Yiting Hao, Jiyan Huang, Fucheng Wang, Weiqiang Zhou, Jingkun Xu, Ximei Liu, Hanjun Yang.  (2023)  Flexible Supercapacitors Based on Stretchable Conducting Polymer Electrodes.  Polymers,  15  (8): (1856).  [PMID:37112003] [10.3390/polym15081856]
2. Biao Ma, Bin Li, Yang Li, Xiaobin Fan, Fengbao Zhang, Guoliang Zhang, Yuanzhi Zhu, Wenchao Peng.  (2021)  Synthesis of nitrogen and sulfur Co-doped carbon with special hollow sphere structure for enhanced catalytic oxidation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119522]
3. Hao Zhan, Jiajun Chen, Chi Zhang, Jincheng Zhang, Li-Juan Fan.  (2021)  Design, Synthesis, and Adhesion of Fluorescent Conjugated Polymers with Pendant Catechol Groups.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.1c00603]
4. Yuhao Zhang, Liang Zhao, Feng Chen, Yongtao Wang, Jinsen Gao, Liyuan Cao, Hui Wang, Chunming Xu.  (2021)  High efficient separation of olefin from fluid catalytic cracking naphtha: Separation mechanism and universal simulation method.  AICHE JOURNAL,  67  (5): (e17153).  [PMID:] [10.1002/aic.17153]
5. Hong Li, Yuhao Zhang, Liang Zhao, Dexin Sun, Jinsen Gao, Chunming Xu.  (2020)  Liquid-liquid equilibria and mechanism exploration for the extraction of sulfides from FCC naphtha via organic solvent as extractant.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2020.114821]
6. Songjie Hua, Yuqi Hu, Liang Zhao, Liyuan Cao, Xiaoqin Wang, Jinsen Gao, Chunming Xu.  (2019)  Selective Removal of Thiophene Using Surface Molecularly Imprinted Polymers Based on β-Cyclodextrin Porous Carbon Nanospheres and Polycarboxylic Acid Functional Monomers.  ENERGY & FUELS,      [PMID:] [10.1021/acs.energyfuels.9b02909]
7. Yuhao Zhang, Hui Wang, Liang Zhao, Jinsen Gao, Chunming Xu.  (2019)  Olefin separation from FCC naphtha by dimethyl sulfoxide: Effect of structure on the separation and correlation of thermodynamic models.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2019.115757]
8. Wen Bing Wu, Sun Xue, Jian Hua Chen, Xiao Li.  (2018)  High removal of thiophene from model gasoline by porous MIL-101(Cr)/SA hybrid membrane.  RSC Advances,  (71): (41003-41011).  [PMID:35557909] [10.1039/C8RA06579A]
9. Xiafei Guo, Faqiong Zhao, Baizhao Zeng.  (2018)  Graphene-doped electrochemical copolymer coating of 2,2-bithiophene and 3-methylthiophene for the highly effective solid-phase microextraction of volatile benzene homologues.  JOURNAL OF SEPARATION SCIENCE,  41  (10): (2197-2206).  [PMID:29436177] [10.1002/jssc.201701330]
10. Shuai Li, Guoliang Liu, Xiuping Ju, Yan Zhang, Jinsheng Zhao.  (2017)  Synthesis, Characterization and Application of Four Novel Electrochromic Materials Employing Nitrotriphenylamine Unit as the Acceptor and Different Thiophene Derivatives as the Donor.  Polymers,  (5): (173).  [PMID:30970853] [10.3390/polym9050173]
11. Xiafei Guo, Aiziguli mulati, Mian Wu, Jie Zhang, Liu Yang, Faqiong Zhao, Baizhao Zeng.  (2017)  An ionic liquid doped electrochemical copolymer coating of indole and 3-methylthiophene for the solid-phase microextraction of polycyclic aromatic hydrocarbons.  RSC Advances,  (36): (22256-22262).  [PMID:] [10.1039/C7RA02372C]
12. Liu Yang, Jie Zhang, Faqiong Zhao, Baizhao Zeng.  (2016)  Electrodeposition of self-assembled poly(3,4-ethylenedioxythiophene) @gold nanoparticles on stainless steel wires for the headspace solid-phase microextraction and gas chromatographic determination of several polycyclic aromatic hydrocarbons.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:27765417] [10.1016/j.chroma.2016.10.041]
13. Junjie Li, Lei Wang, Xiaole Jia, Xiongzhi Xiang, Cheuk-Lam Ho, Wai-Yeung Wong, Hua Li.  (2014)  Preparation and thermoelectric properties of diphenylaminobenzylidene-substituted poly(3-methylthiophene methine)/graphite composite.  RSC Advances,  (107): (62096-62104).  [PMID:] [10.1039/C4RA09621E]
14. Lianyi Xu, Qiang Ye, Xuemin Lu, Qinghua Lu.  (2014)  Electro-Responsively Reversible Transition of Polythiophene Films from Superhydrophobicity to Superhydrophilicity.  ACS Applied Materials & Interfaces,      [PMID:25116074] [10.1021/am5043627]
15. Jie Zhao, Yu Xie, Zhanggao Le, Yan Luo, Yunhua Gao, Rong Zhong, Yuancheng Qin, Jianfei Pan, Yan Huang.  (2013)  Preparation and electromagnetic properties of the BaFe12O19/multiwall carbon nanotubes/poly(3-methyl-thiophene) composites.  POLYMER COMPOSITES,  34  (11): (1801-1808).  [PMID:] [10.1002/pc.22584]
16. Junhao Chen, Yafei Lou, Linan Sun, Azadeh Nilghaz, Shan Liu, Junfei Tian.  (2024)  Precise and efficient release of pilocarpine for sweat wearables.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2024.136403]
17. Yanlong Zhao, Fan Lan, Yunrui Li, Ya Huang, Fei Wang, Kangkang Wang, Rufan Zhang.  (2025)  Coaxial Electroluminochromic Fibers with Dynamic RGB Switching for Pixelated Smart Textiles.  ADVANCED MATERIALS,      [PMID:40557502] [10.1002/adma.202505012]
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