(±)-Camphor - Moligand™, ≥96% , Gating inhibitor of TRPA1;Activator of TRPV1;Activator of TRPV3, CAS No.76-22-2, Gating inhibitor of TRPA1;Activator of TRPV1;Activator of TRPV3

CAS: 76-22-2 Cat. No.: C110690 Peso molecular: 152.23 Beilstein Registry Number: 1907611 Número EC: 200-945-0
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥96%
Synonyms
Alphanon | dl-Camphor (JP17) | 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one | CCG-266237 | CCG-266238 | NCGC00090730-02 | KBio1_000724 | Sarna (Salt/Mix) | Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)- | SYNTHETIC CAMPHOR | C1251 | Camphor, (1R,4R)-(+)
Storage
Room temperature
Shipped In
Normal
Size
Estado
Price
Qty
100g
C110690-100g
3

16,90US$

25,90US$
Guardar 9,00 US$ (34.75%)
500g
C110690-500g
3

33,90US$

50,90US$
Guardar 17,00 US$ (33.40%)
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥96% 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 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Camphor is a novel carbon nanotube precursor.
Camphor was used in the synthesis of single-walled nanotubes by chemical vapor deposition. It was used in two-phase based hollow fibre liquid-phase microextraction procedure for migration analysis of food packagings containing essential oils.

Specifications

Sinónimos
Alphanon | dl-Camphor (JP17) | 1, 7, 7-Trimethylbicyclo[2.2.1]heptan-2-one | CCG-266237 | CCG-266238 | NCGC00090730-02 | KBio1_000724 | Sarna (Salt/Mix) | Bicyclo[2.2.1]heptan-2-one, 1, 7, 7-trimethyl-, (1R)- | SYNTHETIC CAMPHOR | C1251 | Camphor, (1R, 4R)-(+)
Especificaciones y pureza
Moligand™, ≥96%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Moligand™
Tipo de acción
ACTIVATOR, GATING INHIBITOR
Mecanismo de acción
Gating inhibitor of TRPA1;Activator of TRPV1;Activator of TRPV3
Pureza
≥96%
Nombres e identificadores
Pubchem Sid504750577
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750577
Sonrisas canónicasCC1(C2CCC1(C(=O)C2)C)C
IUPAC Name1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
InChIKeyDSSYKIVIOFKYAU-UHFFFAOYSA-N
INCHI1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3
Isómeros SMILES CC1(C2CCC1(C(=O)C2)C)C
WGK Alemania 3
RTECS EX1225000
CAS alternativo 21368-68-3
Número ONU 2717
Grupo de embalaje III
Peso molecular 152.23
Beilstein 1907611
Reaxy-Rn 1907611
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907611&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 ParentBicyclic monoterpenoids
Alternative Parents Ketones  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Bicyclic monoterpenoid - Bornane monoterpenoid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
External Descriptors a small molecule
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)
TRPV1 Tclin Transient receptor potential cation channel subfamily V member 1 (0 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)
Objetivos asociados (no humanos)
Plasmodium berghei (192651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 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.

18 results found

Lot NumberCertificate TypeFechaArticulo
D2624073Certificate of AnalysisSep 24, 2025 C110690
G2603067Certificate of AnalysisSep 24, 2025 C110690
J2515299Certificate of AnalysisSep 24, 2025 C110690
J2515298Certificate of AnalysisSep 24, 2025 C110690
J2515297Certificate of AnalysisSep 24, 2025 C110690
I2107237Certificate of AnalysisJun 11, 2025 C110690
D2530115Certificate of AnalysisJul 08, 2024 C110690
D2530116Certificate of AnalysisJul 08, 2024 C110690
C2513194Certificate of AnalysisOct 26, 2023 C110690
K2320053Certificate of AnalysisOct 26, 2023 C110690
K2320050Certificate of AnalysisOct 26, 2023 C110690
I2425201Certificate of AnalysisOct 26, 2023 C110690
E2509040Certificate of AnalysisOct 26, 2023 C110690
C23101309Certificate of AnalysisMar 16, 2023 C110690
H2224246Certificate of AnalysisAug 26, 2022 C110690
J1823094Certificate of AnalysisAug 11, 2022 C110690
J2312041Certificate of AnalysisSep 11, 2021 C110690
I2107238Certificate of AnalysisSep 11, 2021 C110690

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Propiedades químicas y físicas
SolubilidadSolubility in water: 1.5 g/L (20°C) Solubility in other solvents: at 25°C 1 g dissolves in 1 ml Alcohol, 1 ml Ether, 0.5 ml Chloroform, 0.4 ml Benzene, 0.4 ml Acetone, 1.5 ml Turpentine oil, 0.5 ml Glacial acetic acid.
SensibilidadMoisture sensitive.
Punto de inflamación (°F)147.2 °F
Punto de inflamación (°C)65.5℃
Punto de ebullición (°C)204°C
Punto de fusión (°C)175-177°C
Peso molecular152.230 g/mol
XLogP32.200
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass152.12 Da
Monoisotopic Mass152.12 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count11
Formal Charge0
Complexity217.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
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. Shishi Shao, Jiaqiang Zhao, Wei Wang, Hanbing Nie, Yan Jie Li, Xuepeng Zhang, Cheng Zhi Huang, Peng Fei Gao.  (2023)  Ratiometric room-temperature phosphorescence platform for visual and spectral analysis of naphthalene.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2023.135047]
2. Yuyan Cai, Haozhe Xu, Chenyi Xu, Zhaojiang Zuo.  (2023)  Adjusting function of camphor on primary metabolism in Cinnamomum camphora stressed by high temperature.  PLANT SCIENCE,      [PMID:38101618] [10.1016/j.plantsci.2023.111956]
3. Tianyu Huang, Meng Lai, Zhenwei Lin, Ruiqi Luo, Xuezheng Xiang, Haozhe Xu, Ning Pan, Zhaojiang Zuo.  (2023)  Identification of algicidal monoterpenoids from four chemotypes of Cinnamomum camphora and their algicidal mechanisms on Microcystis aeruginosa.  ENVIRONMENTAL RESEARCH,      [PMID:37989462] [10.1016/j.envres.2023.117714]
4. Qian Pan, Junhui Hu, Chengzhi Hu, Ying Yan.  (2023)  Reparation and characterization of carbon nanotubes coated on expanded perlite as sound absorption composite materials.  Materials Science and Engineering B-Advanced Functional Solid-State Materials,      [PMID:] [10.1016/j.mseb.2023.116697]
5. Chengzhi Hu, Huiping Zhang, Ying Yan.  (2023)  Toluene combustion over Co3O4-CNTs/PSSF catalysts and investigation of the effects of acid treatment on catalytic activity.  Journal of the Taiwan Institute of Chemical Engineers,      [PMID:] [10.1016/j.jtice.2023.105002]
6. Xiaomin Zhang, Gaofeng Hu, Chaoyang Xu, Wen Nie, Kezhou Cai, Hongmei Fang, Baocai Xu.  (2023)  Inhibition of benzo[a]pyrene formation in charcoal-grilled pork sausages by ginger and its key compounds.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  103  (6): (2838-2847).  [PMID:36700254] [10.1002/jsfa.12470]
7. Ying Yan, Chengzhi Hu, Zijian Wang, Huiping Zhang.  (2023)  Mass transfer enhancement of toluene adsorption over CNTs films on paper-like sintered stained steel fibers.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2023.130955]
8. 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]
9. Xinying Duan, Li Zhang, Hongyan Si, Jie Song, Peng Wang, Shangxing Chen, Hai Luo, Xiaoping Rao, Zongde Wang, Shengliang Liao.  (2022)  Synthesis, Antifungal Activity, Cytotoxicity and QSAR Study of Camphor Derivatives.  Journal of Fungi,  (8): (762).  [PMID:35893130] [10.3390/jof8080762]
10. 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]
11. Xu Chenyi, Ma Yuandan, Tian Zhengfeng, Luo Qingyun, Zheng Tiefeng, Wang Bin, Zuo Zhaojiang.  (2021)  Monoterpene emissions and their protection effects on adult Cinnamomum camphora against high temperature.  TREES-STRUCTURE AND FUNCTION,  36  (2): (711-721).  [PMID:] [10.1007/s00468-021-02242-4]
12. 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]
13. Zhengfeng Tian, Qingyun Luo, Zhaojiang Zuo.  (2021)  Seasonal emission of monoterpenes from four chemotypes of Cinnamomum camphora.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2021.113327]
14. Xiao‑Yu Li, Li Xu, Hong‑Li Li, Jing Du, Xue‑Song Liu, Feng‑Hua Li.  (2017)  Au-poly(lactic-co-glycolic) acid complex nanoparticles as ultrasound contrast agents: Preparation, characterization and in vitro study.  Molecular Medicine Reports,  17  (3): (3763-3768).  [PMID:29286171] [10.3892/mmr.2017.8351]
15. Junling He, Yong Tang, Chiliang Lin, Shaoyun Peng, Stig Pedersen-Bjergaard, Frederik André Hansen, Chen Zhou.  (2024)  Electromembrane extraction of multi-class prohibited/restricted veterinary drugs from food samples – Exploring liquid membrane composition.  FOOD CHEMISTRY,      [PMID:39733624] [10.1016/j.foodchem.2024.142680]
16. You Zhou, De Qiang Qin, Min Xing Zhang, Miao Sun, Lu Sheng Wan, Jing Sheng Chen.  (2024)  Exploring bioactive molecules with fumigation toxicity against the red imported fire ant Solenopsis invicta Buren from commercial essential oils by GC–MS combined with chemometrics.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2023.117993]
Calculadoras de soluciones
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