DL-Menthol - Moligand™, analytical standard , Activator of TRPA1;Gating inhibitor of TRPA1;Activator of TRPM8;Activator of TRPV3, CAS No.89-78-1, Activator of TRPA1;Gating inhibitor of TRPA1;Activator of TRPM8;Activator of TRPV3

CAS: 89-78-1 Cat. No.: M105139 Peso molecular: 156.27 Beilstein Registry Number: 3194263 Número EC: 201-939-0
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
AKOS016843634 | DTXCID30805 | HY-75161 | MENTHOL, UNSPECIFIED FORM | DTXSID8029650 | Menthol (USP) | DL-Menthol, analytical standard | Menthol racemate | 5-methyl-2-(propan-2-yl)cyclohexan-1-ol | Fisherman's friend lozenges | MFCD00062979 | BBL009325 | Cy
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
20mg
M105139-20mg
4
49,90US$
100mg
M105139-100mg
3
148,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, analytical standard Analytical standard,Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 23 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

DL-Menthol triggers cold-sensitive TRPM8 receptors in the skin neurons in vitro. The (-)-Menthol form exists naturally in nature, primarily found in fruit extracts or spearmint extracts. This racemic mixture could theoretically be created by the hydrogenation of the monoterpene pulegone.
A chemical which triggers cold-sensitive TRPM8 receptors in the skin neurons in vitro.

Specifications

Sinónimos
AKOS016843634 | DTXCID30805 | HY-75161 | MENTHOL, UNSPECIFIED FORM | DTXSID8029650 | Menthol (USP) | DL-Menthol, analytical standard | Menthol racemate | 5-methyl-2-(propan-2-yl)cyclohexan-1-ol | Fisherman's friend lozenges | MFCD00062979 | BBL009325 | Cy
Especificaciones y pureza
Moligand™, analytical standard
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Analytical standard, Moligand™
Tipo de acción
ACTIVATOR, GATING INHIBITOR
Mecanismo de acción
Activator of TRPA1;Gating inhibitor of TRPA1;Activator of TRPM8;Activator of TRPV3
Nombres e identificadores
Sonrisas canónicasCC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
IUPAC Name5-methyl-2-propan-2-ylcyclohexan-1-ol
InChIKeyNOOLISFMXDJSKH-UHFFFAOYSA-N
INCHI1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3
Isómeros SMILES CC1CCC(C(C1)O)C(C)C
WGK Alemania 2
RTECS OT0350000
CAS alternativo 15356-70-4;1490-04-6
Peso molecular 156.27
Beilstein 3194263
Reaxy-Rn 1902293
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1902293&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
SuperclassLipids and lipid-like molecules
ClasePrenol lipids
SubclassMonoterpenoids
Intermediate Tree Nodes Not available
Direct ParentMenthane monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Cyclohexanols  Cyclic alcohols and derivatives  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexanol - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
External Descriptors a monoterpenol
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TRPV3 Tchem Transient receptor potential cation channel subfamily V member 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TRPM8 Tclin Transient receptor potential cation channel subfamily M member 8 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (787 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A3 Tbio UDP-glucuronosyltransferase 1-3 (217 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cutibacterium acnes (887 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Spodoptera littoralis (798 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cavia porcellus (23802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Musca domestica (713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tetranychus urticae (2600 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rdl GABA receptor subunit (76 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpm8 Transient receptor potential cation channel subfamily M member 8 (889 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colletotrichum gloeosporioides (560 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Culex pipiens (191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leptinotarsa decemlineata (1161 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Psoroptes ovis (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lipaphis erysimi (85 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Theba pisana (23 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.

4 results found

Lot NumberCertificate TypeFechaArticulo
E2508295Certificate of AnalysisApr 27, 2025 M105139
E2508296Certificate of AnalysisApr 27, 2025 M105139
L1912138Certificate of AnalysisJul 12, 2023 M105139
K2006186Certificate of AnalysisSep 09, 2022 M105139
Propiedades químicas y físicas
SolubilidadSoluble in water (partly), and alcohol.
Punto de inflamación (°F)199.4 °F
Punto de inflamación (°C)93 °C
Punto de ebullición (°C)216°C
Punto de fusión (°C)32-36°C
Peso molecular156.260 g/mol
XLogP33.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass156.151 Da
Monoisotopic Mass156.151 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity120.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count3
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. Zhou Qian, Su XiaoLu, Yao YanXing, He Bin, Jin FengMei, Gao MengYue, Wang Qi, Feng GuiPing, Li BaoXi, Liu Rui, Dong Jun.  (2023)  Preparation of a hydrophobic deep eutectic solvent and its application in the detection of quinolone residues in cattle urine.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  415  (17): (3581-3592).  [PMID:37243734] [10.1007/s00216-023-04749-w]
2. Jingyu Zhang, Zhihui Zhang, Liping Yao, Mingrong Qian, Zuguang Li, Yulin Han, Shanshan Bai, Mawrong Lee.  (2023)  pH-responsive switchable deep eutectic solvents to mediate pretreatment method for trace analysis of triazole fungicides in peel wastes.  FOOD CHEMISTRY,      [PMID:36682163] [10.1016/j.foodchem.2023.135486]
3. Meichao Liao, Lin Yang, Xiaoyue Yang, Erxu Wang, Bin Lu, Jiye Wang, Li Duan.  (2022)  Vortex-assisted liquid–liquid microextraction based on hydrophobic deep eutectic solvent for the urinary excretion study of Taraxacum mongolicum extract in rats.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2022.108167]
4. Wen-wen Deng, Xue-ping Mei, Zi-jun Cheng, Tian-xiang gan, Xuan Tian, Jiang-nan Hu, Chuan-ru Zang, Bo Sun, Jing Wu, Yin Deng, Reza. A. Ghiladi, George H. Lorimer, Gizem Keceli, Jun Wang.  (2022)  Extraction of weak hydrophobic sulforaphane from broccoli by salting-out assisted hydrophobic deep eutectic solvent extraction.  FOOD CHEMISTRY,      [PMID:36370577] [10.1016/j.foodchem.2022.134817]
5. Heng Lu, Xiaohong Tan, Guobin Huang, Shaoru Wu, Yanmei Zhou, Junying Zhang, Qiaowen Zheng, Tianju Chen, Feiming Li, Zhixiong Cai, Jingbin Zeng, Maosheng Zhang.  (2022)  Green synthesis of highly stable CsPbBr3 perovskite nanocrystals using natural deep eutectic solvents as solvents and surface ligands.  Nanoscale,  14  (46): (17222-17229).  [PMID:36250272] [10.1039/D2NR04173A]
6. Jiaze Yan, Shaomin Ma, Mingrui Feng, Jiqi Zheng, Ming Guo.  (2022)  Hydrophobic deep eutectic solvent-based ultrasonic-assisted liquid-liquid microextraction combined with GC for eugenol, isoeugenol, and methyl isoeugenol determination in aquatic products.  Food Additives and Contaminants Part A-Chemistry Analysis Control Exposure & Risk Assessment,      [PMID:35997563] [10.1080/19440049.2022.2112764]
7. Meichao Liao, Yang Zhao, Xiaoyue Yang, Lin Yang, E-Hu Liu, Bin Lu, Jiye Wang, Xiaopeng Liu, Yanzhong Chang, Li Duan.  (2022)  A greener and sustainable route for medicinal plant analysis: Recycle utilization of hydrophobic deep eutectic solvent.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2022.107372]
8. Tian Quan, Dandan Wang, Lijuan Yang, Shaochi Liu, Yongqin Tao, Junji Wang, Linlin Deng, Xun Kang, Kailian Zhang, Zhining Xia, Die Gao.  (2021)  Effective extraction methods based on hydrophobic deep eutectic solvent coupled with functional molecularly imprinted polymers: Application on quercetagetin extraction from natural medicine and blood.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2021.107076]
9. Jing Li, Yanjun Jiao, Qin Luo, Weixin Hu, Shenwen Fang, Chunling Tang, Qiang Liu.  (2021)  Treatment of oil-based drill cuttings by hydrophobic deep eutectic solvents.  CANADIAN JOURNAL OF CHEMICAL ENGINEERING,  100  (8): (1747-1754).  [PMID:] [10.1002/cjce.24263]
10. Tong Wang, Qing Wang, Qing Guo, Ping Li, Hua Yang.  (2021)  A hydrophobic deep eutectic solvents-based integrated method for efficient and green extraction and recovery of natural products from Rosmarinus officinalis leaves, Ginkgo biloba leaves and Salvia miltiorrhiza roots.  FOOD CHEMISTRY,      [PMID:34144425] [10.1016/j.foodchem.2021.130282]
11. Ge Dandan, Gao Ying, Cao Yunxin, Dai Enrui, Yuan Lin.  (2020)  Preparation of a New Polymeric Deep Eutectic Solvent and Its Application in Vortex-Assisted Liquid-Liquid Microextraction of Parabens in Foods, Cosmetics and Pharmaceutical Products.  JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY,  31  (10): (2120-2128).  [PMID:] [10.21577/0103-5053.20200113]
12. Yingjie Zhang, Li Kang, Huajun Huang, Jianping Deng.  (2020)  Optically Active Janus Particles Constructed by Chiral Helical Polymers through Emulsion Polymerization Combined with Solvent Evaporation-Induced Phase Separation.  ACS Applied Materials & Interfaces,      [PMID:31939279] [10.1021/acsami.9b21222]
13. Ge Dandan, Wang Ying, Jiang Qian, Dai Enrui.  (2019)  A Deep Eutectic Solvent as an Extraction Solvent to Separate and Preconcentrate Parabens in Water Samples Using in situ Liquid-Liquid Microextraction.  JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY,  30  (6): (1203-1210).  [PMID:] [10.21577/0103-5053.20190014]
14. Dandan Ge, Yi Zhang, Yixiu Dai, Shumin Yang.  (2017)  Air-assisted dispersive liquid–liquid microextraction based on a new hydrophobic deep eutectic solvent for the preconcentration of benzophenone-type UV filters from aqueous samples.  JOURNAL OF SEPARATION SCIENCE,  41  (7): (1635-1643).  [PMID:29282887] [10.1002/jssc.201701282]
15. Linzhou Zhuang, Beibei Ma, Siyu Chen, Xunan Hou, Shuixia Chen.  (2015)  Fast synthesis of mesoporous silica materials via simple organic compounds templated sol–gel route in the absence of hydrogen bond.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2015.04.007]
16. Jiaze Yan, Chao Jiang, Jiqi Zheng, Ming Guo.  (2025)  Enhanced microdialysis based on hydrophobic deep eutectic solvents for sampling of eugenol in Glyptocidaris crenularis.  ANALYTICA CHIMICA ACTA,      [PMID:40021328] [10.1016/j.aca.2025.343774]
17. Yuxin Liu, Chenjie Ma, Mantang Chen, Jufang Hao, Wei Liu, Jingjing Yu.  (2025)  Hydrophobic deep eutectic solvent-based ferrofluid for the multi-residue analysis of pyrethroid insecticides in agricultural products: Facile pretreatment and MS-friendly detection.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40773813] [10.1016/j.chroma.2025.466262]
18. Xiaoyan Jiang, Renxiu Huang, Guohua Zhu, Lingqi Shen, Panfei Li, Xuerong Yang, Fangxi Xu, Zuguang Li.  (2025)  Determination of liquid crystal monomers in environmental water by ultrasound-assisted pH-responsive deep eutectic solvent based homogeneous liquid-liquid microextraction.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40819546] [10.1016/j.chroma.2025.466279]
19. Yan Li, Kun Hu, Chao Huang, Yong Hu, Hongwu Ji, Shucheng Liu, Jing Gao.  (2022)  Improvement of solubility, stability and antioxidant activity of carotenoids using deep eutectic solvent-based microemulsions.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:35679734] [10.1016/j.colsurfb.2022.112591]
20. Zixing Zhang, Yuxin Xu, Yun Hu.  (2025)  Enhancing the water resistance and functional properties of chitosan-based films using a hydrophobic deep eutectic solvent.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40446998] [10.1016/j.ijbiomac.2025.144776]
21. Yan Zhou, Xujing Dong, Xiaoyi Tian, Shuai Wang, Fanqing Meng, Jianguang Qi, Yinglong Wang, Ekemini Ituen.  (2025)  Highly efficient separation of adipic and glutaric acids from aqueous solutions by phosphonate-based deep eutectic solvents: Experimental and molecular insights.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.136258]
22. Yalu Liu, Zhenpeng Wang, Yapeng Zhang, Jiutao Hu, Sen Huang, Bin Hao, Xiaobo Huang.  (2025)  Photocurable 3D-Printed Hydrophobic Eutectic Gels for Underwater Wearable Sensors.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.139322]
23. Minjie Gao, Congfei Zhu, Yasen Dai, Bingru Wang, Shuhang Ren, Weize Wu.  (2026)  Physicochemical Properties of Ethylene Glycol-Based Deep Eutectic Solvents for CO2 Capture.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.5c00729]
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