3-Methylindole - 10mM in DMSO , CAS No.83-34-1

CAS: 83-34-1 Cat. No.: M426157 Peso molecular: 131.17 Beilstein Registry Number: 111296 Número EC: 201-471-7
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
BRD-K73824630-001-03-2 | s4959 | .beta.-Methylindole | 3-Methylindole, 98% | CCG-214598 | FEMA No. 3019 | Skatole, >=98% | M-3898 | WLN: T56 BMJ D1 | C08313 | DTXCID601775 | CHEBI:9171 | HSDB 3511 | SKATOLUM | 3-methyl indole | M0347 | CG-0502 | HY-W00735
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
Size
Estado
Price
Qty
1ml
M426157-1ml
1

120,90US$

176,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

3-Methylindole is a naturally abundant pneumotoxin. In lower concentrations, the compound has a pleasant aroma, giving orange blossoms and jasmine their pleasing scent.
A naturally abundant pneumotoxin.

Specifications

Sinónimos
BRD-K73824630-001-03-2 | s4959 | .beta.-Methylindole | 3-Methylindole, 98% | CCG-214598 | FEMA No. 3019 | Skatole, >=98% | M-3898 | WLN: T56 BMJ D1 | C08313 | DTXCID601775 | CHEBI:9171 | HSDB 3511 | SKATOLUM | 3-methyl indole | M0347 | CG-0502 | HY-W00735
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Pubchem Sid528759036
Sonrisas canónicasCC1=CNC2=CC=CC=C12
IUPAC Name3-methyl-1H-indole
InChIKeyZFRKQXVRDFCRJG-UHFFFAOYSA-N
INCHI1S/C9H9N/c1-7-6-10-9-5-3-2-4-8(7)9/h2-6,10H,1H3
Isómeros SMILES CC1=CNC2=CC=CC=C12
WGK Alemania 2
RTECS NM0350000
Peso molecular 131.17
Beilstein 111296
Reaxy-Rn 111296
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=111296&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
ClaseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes 3-alkylindoles
Direct Parent3-methylindoles
Alternative Parents Substituted pyrroles  Benzenoids  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 3-methylindole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 3-methylindoles. These are aromatic heterocyclic compounds that contain an indole moiety substituted at the 3-position with a methyl group.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATM Tchem Serine-protein kinase ATM (4198 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
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.

1 results found

Lot NumberCertificate TypeFechaArticulo
J2210002Certificate of AnalysisMay 20, 2026 M426157
Propiedades químicas y físicas
SensibilidadLight & Air Sensitive.
Punto de inflamación (°F)269.6 °F
Punto de inflamación (°C)132℃
Punto de ebullición (°C)265-266°C
Punto de fusión (°C)95°C
Peso molecular131.170 g/mol
XLogP32.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass131.073 Da
Monoisotopic Mass131.073 Da
Topological Polar Surface Area15.800 Ų
Heavy Atom Count10
Formal Charge0
Complexity122.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Bingbing Luo, Kai Wu, Jiajun Yu, Siyu Wang, Yihan Wang, Chenyang Chu, Huiyan Zhang.  (2022)  Enhancement of renewable N-heterocycles production via catalytic co-pyrolysis of glycerol and cellulose over HZSM-5 under ammonia atmosphere.  JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,      [PMID:] [10.1016/j.jaap.2022.105649]
2. Qiao Ma, Nan Meng, Jiancheng Su, Yujie Li, Jiazheng Gu, Yidi Wang, Jingwei Wang, Yuanyuan Qu, Zelong Zhao, Yeqing Sun.  (2022)  Unraveling the skatole biodegradation process in an enrichment consortium using integrated omics and culture-dependent strategies.  Journal of Environmental Sciences,      [PMID:36522097] [10.1016/j.jes.2022.06.025]
3. Jia Yin, Yujie Song, Yaozhong Hu, Yuanyifei Wang, Bowei Zhang, Jin Wang, Xuemeng Ji, Shuo Wang.  (2021)  Dose-Dependent Beneficial Effects of Tryptophan and Its Derived Metabolites on Akkermansia In Vitro: A Preliminary Prospective Study.  Microorganisms,  (7): (1511).  [PMID:34361945] [10.3390/microorganisms9071511]
4. Yanjuan Gao, Guoying Wang, Aijuan Zhou, Xiuping Yue, Yanqing Duan, Xin Kong, Xiao Zhang.  (2019)  Effect of nitrate on indole degradation characteristics and methanogenesis under mixed denitrification and methanogenesis culture.  BIOCHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.bej.2019.02.009]
5. Zhang S., Quan Y., Song L., Duan P., Fan Y.-Сh..  (2017)  Three-Dimensional Fluorescence Characteristics of Algal Bio-Oil.  Journal of Applied Spectroscopy,  84  (3): (508-511).  [PMID:] [10.1007/s10812-017-0501-8]
6. Qian Yao, Lujiang Xu, Zheng Han, Ying Zhang.  (2015)  Production of indoles via thermo-catalytic conversion and ammonization of bio-derived furfural.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2015.05.094]
7. Pengfei Ma, Wenming Yang, Ting Fan, Hong Liu, Zhiping Zhou, Jinhui Li, Lin Zhang, Wanzhen Xu.  (2015)  Surface imprinted polymers for oil denitrification with the combination of computational simulation and multi-template molecular imprinting.  POLYMERS FOR ADVANCED TECHNOLOGIES,  26  (5): (476-486).  [PMID:] [10.1002/pat.3476]
8. Lukuan Liu, Yang Cao, Pengfei Ma, Chunxiao Qiu, Wanzhen Xu, Hong Liu, Weihong Huang.  (2013)  Rational design and preparation of magnetic imprinted polymers for removal of indole by molecular simulation and improved atom transfer radical polymerization.  RSC Advances,  (2): (605-616).  [PMID:] [10.1039/C3RA43875A]
9. Yufei Deng, Xiaoying Hou, Qian Fang, Haiping Wang, Xiaoxuan Li, Zhiyong Hu, Zhaolu Liu, Limei Fan, Yunyi Liu, Zhengqi Fu, Xiji Shu, Binlian Sun, Lijun Huang, Yuchen Liu.  (2025)  High-salt diet decreases FOLFOX efficacy via gut bacterial tryptophan metabolism in colorectal cancer.  MOLECULAR MEDICINE,      [PMID:39972411] [10.1186/s10020-025-01122-8]
10. Yuan-yuan Zhai, Qiang Wang, Qi-yao Nong, Mei-yu Gao, Ying Zhang, Qin-wen Xiao, Yuan Tian, Zun-jian Zhang, Feng-guo Xu, Pei Zhang.  (2025)  Pitavastatin overcomes multi-drug resistance in CRC and NSCLC by targeting the NRP1-ZFX axis.  BIOCHEMICAL PHARMACOLOGY,      [PMID:40684995] [10.1016/j.bcp.2025.117183]
11. Miao Tian, Mingchao Li, Hongxia Tan, Tianying Lu, Lintao Zeng.  (2025)  A portable, reusable, and highly sensitive colorimetric probe for rapid screening of meat freshness.  FOOD CONTROL,      [PMID:] [10.1016/j.foodcont.2025.111803]
12. Nan Meng, Genxiu Li, Jiaxin Zhang, Jingwen Zhu, Xutong Kang, Jiahao Duan, Qiao Ma.  (2026)  A novel and evolutionarily distinct flavoprotein monooxygenase drives skatole degradation in Rhodococcus.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,      [PMID:] [10.1128/aem.00228-26]
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