D-Menthol - ≥99% , Activator of TRPM8, CAS No.15356-60-2, Activator of TRPM8

CAS: 15356-60-2 Cat. No.: M105270 Peso molecular: 156.27 Beilstein Registry Number: 1902292 Número EC: 239-387-8 PubChem CID: 165675
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
M3170 | UNII-C6B1OE8P3W | (1S,2R,5S)-2-Isopropyl-5-methylcyclohexanol | A815982 | (1S,2R,5S)-5-methyl-2-(propan-2-yl)cyclohexan-1-ol | (1S,2R,5S)-Menthol | (1S,2R,5S)-(+)-Menthol, 99% | (1S,2R,5S)-2-Isopropyl-5-methylcyclohexan-1-ol | Menthol, cis-1,3,tra
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
M105270-5g
1

43,90US$

55,90US$
Guardar 12,00 US$ (21.47%)
25g
M105270-25g
2

158,90US$

199,90US$
Guardar 41,00 US$ (20.51%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

(1S,2R,5S)-(+)-menthol is a chiral secondary alcohol. Its alcohol group can be protected as 2-tetrahydrofuranyl ether by reacting with bromotrichloromethane and tetrahydrofuran.

(1S,2R,5S)-(+)-menthol can undergo acylation with acid anhydrides in the presence of trimethylsilyl trifluoromethanesulfonate to form the corresponding acylated products.


Specifications

Sinónimos
M3170 | UNII-C6B1OE8P3W | (1S, 2R, 5S)-2-Isopropyl-5-methylcyclohexanol | A815982 | (1S, 2R, 5S)-5-methyl-2-(propan-2-yl)cyclohexan-1-ol | (1S, 2R, 5S)-Menthol | (1S, 2R, 5S)-(+)-Menthol, 99% | (1S, 2R, 5S)-2-Isopropyl-5-methylcyclohexan-1-ol | Menthol, cis-1, 3, tra
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
ACTIVATOR
Mecanismo de acción
Activator of TRPM8
Pureza
≥99%
Nombres e identificadores
Sonrisas canónicasCC1CCC(C(C1)O)C(C)C
IUPAC Name(1S,2R,5S)-5-methyl-2-propan-2-ylcyclohexan-1-ol
InChIKeyNOOLISFMXDJSKH-AEJSXWLSSA-N
INCHI1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m0/s1
Isómeros SMILES C[C@H]1CC[C@@H]([C@H](C1)O)C(C)C
WGK Alemania 2
RTECS OT0700000
CAS alternativo 15356-70-4,15356-60-2,89-78-1
PubChem CID 165675
Peso molecular 156.27
Beilstein 1902292

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 p-menthan-3-ol
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TRPM8 Tclin Transient receptor potential cation channel subfamily M member 8 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
D23181095Certificate of AnalysisDec 26, 2022 M105270
D23181269Certificate of AnalysisDec 21, 2022 M105270
D23181273Certificate of AnalysisDec 21, 2022 M105270
L22151038Certificate of AnalysisNov 21, 2022 M105270
L2215945Certificate of AnalysisNov 21, 2022 M105270
G2219750Certificate of AnalysisJul 04, 2022 M105270
G2219751Certificate of AnalysisJul 04, 2022 M105270
Propiedades químicas y físicas
SolubilidadSoluble in methanol (almost transparency), chloroform, alcohols, water (456 mg/l at 25 °C), and ether.
Rotación específica [α]50 ° (C=10, EtOH)
Punto de inflamación (°F)213.8 °F
Punto de inflamación (°C)101 °C
Punto de ebullición (°C)103-104 °C/9 mmHg
Punto de fusión (°C)42°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 Count3
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. Yi Chen, Xuan Wang, Hongyang Ma, Shyam Venkateswaran, Benjamin S. Hsiao.  (2025)  Chiral electrospun nanofibrous membranes for selective adsorption of chiral compounds.  POLYMER,      [PMID:] [10.1016/j.polymer.2025.128893]
2. Xiaofei Shen, Hailong Huang, Hao Qian, Longxiang Tang, Yan Zhang, Min Xu, Huiqing Wang, Zhongkai Wang.  (2021)  Super Chirality Promotion of Helical Poly(Phenyl Isocyanide)s by Grafting onto Ethyl Cellulose.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  222  (15): (2100103).  [PMID:] [10.1002/macp.202100103]
3. Hao Qian, Xiaofei Shen, Hailong Huang, Yan Zhang, Mingtao Zhang, Huiqing Wang, Zhongkai Wang.  (2019)  Helical poly(phenyl isocyanide)s grafted selectively on C-6 of cellulose for improved chiral recognition ability.  CARBOHYDRATE POLYMERS,      [PMID:31888853] [10.1016/j.carbpol.2019.115737]
4. Jiawei Zhou, Yumin Sang, Zhuang Wang, Jiacheng Feng, Linjiang Zhu, Xiaolong Chen.  (2024)  Enhancing the Enantioselectivity and Catalytic Efficiency of Esterase from Bacillus subtilis for Kinetic Resolution of l-Menthol through Semirational Design.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:38235660] [10.1021/acs.jafc.3c08321]
5. Zang Yu, Hou Rui, Wei Bohua, Liu Yuting, Wang Jianjun, Liu Jiao, Xu Liang, Zhang Wei.  (2026)  Cascade-controlled porous composite membranes: pore-supporting synergy enabling high-flux enantioseparation of amino acids and pharmaceuticals.  Science China-Materials,      [PMID:] [10.1007/s40843-025-3936-8]
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