Borneol - ≥55% , CAS No.507-70-0

CAS: 507-70-0 Cat. No.: B109561 Molecular Weight: 154.25 Beilstein Registry Number: 6,73 EC Number: 208-080-0
AVAILABLE TO ORDER
GRADE & PURITY ≥55%
Synonyms
Endo-2-camphanol | 4,7,7-trimethylbicyclo[2.2.1]heptan-3-ol | AC-34416 | SR-05000002386 | SCHEMBL56714 | (+)-Borneol 100 microg/mL in Methanol | Bingpia | exo-2-Bornanol | BORNEOL, (L) | Endo-2-hydroxycamphane | CCG-231498 | AKOS017278270 | BBL028096 | En
Storage
Store at 2-8°C
Shipped In
Wet ice,FedEx DG Service
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25g
B109561-25g
1
$15.90
100g
B109561-100g
2
$27.90
250g
B109561-250g
1
$54.90
500g
B109561-500g
2
$72.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥55% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice,FedEx DG Service 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.

Specifications

Synonyms
Endo-2-camphanol | 4, 7, 7-trimethylbicyclo[2.2.1]heptan-3-ol | AC-34416 | SR-05000002386 | SCHEMBL56714 | (+)-Borneol 100 microg/mL in Methanol | Bingpia | exo-2-Bornanol | BORNEOL, (L) | Endo-2-hydroxycamphane | CCG-231498 | AKOS017278270 | BBL028096 | En
Specifications & Purity
≥55%
Storage
Store at 2-8°C
Shipped In
Wet ice, FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
MODULATOR
Purity
≥55%
Names and Identifiers
Canonical SmilesCC1(C2CCC1(C(C2)O)C)C
IUPAC Name1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
InChIKeyDTGKSKDOIYIVQL-UHFFFAOYSA-N
INCHI1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3
Isomeric SMILES CC1(C2CCC1(C(C2)O)C)C
RTECS ED7000000
UN Number 1312
Packing Group III
Molecular Weight 154.25
Beilstein 6,73
Reaxy-Rn 6052111
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6052111&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
ClassPrenol lipids
SubclassMonoterpenoids
Intermediate Tree Nodes Not available
Direct ParentBicyclic monoterpenoids
Alternative Parents Secondary alcohols  Cyclic alcohols and derivatives  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Bicyclic monoterpenoid - Bornane monoterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
DescriptionThis 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 monoterpenol
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
Pyricularia grisea (1253 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Phytophthora infestans (820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cutibacterium acnes (887 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Puccinia recondita (281 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Blumeria graminis (462 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tetranychus urticae (2600 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 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
Fusarium culmorum (260 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium oxysporum f. sp. lycopersici (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leptinotarsa decemlineata (1161 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium graminearum (1554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Corticium (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pythium (470 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

10 results found

Lot NumberCertificate TypeDateItem
I2202446Certificate of AnalysisJun 11, 2026 B109561
I2202447Certificate of AnalysisJun 11, 2026 B109561
I2202448Certificate of AnalysisJun 11, 2026 B109561
F2109018Certificate of AnalysisMar 04, 2025 B109561
F2109019Certificate of AnalysisMar 04, 2025 B109561
B2428016Certificate of AnalysisJul 23, 2022 B109561
C2517138Certificate of AnalysisJul 23, 2022 B109561
H2401006Certificate of AnalysisJul 23, 2022 B109561
I2202685Certificate of AnalysisJul 23, 2022 B109561
C2211234Certificate of AnalysisMay 06, 2021 B109561
Chemical and Physical Properties
SolubilityInsoluble in water; Very soluble in Benzene,Ether,Alcohol; Soluble in Toluene,Acetone,Chloroform
Boil Point(°C)212°C
Melt Point(°C)208°C
Molecular Weight154.250 g/mol
XLogP32.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass154.136 Da
Monoisotopic Mass154.136 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity185.000
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
Citations of This Product
References
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. Chuanhui Teng, Wei Lv, Yuqin Chen, Linfeng Liu, Jiaqing Yin, Shengnan Li, Zhiyi Min, Qi Zhang, Weichong He, Kunfang Ma, Xinrui Li, Xiang Cao, Hongliang Xin.  (2023)  Enhanced the treatment of ischemic stroke through intranasal temperature-sensitive hydrogels of edaravone and borneol inclusion complex.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:38154533] [10.1016/j.ijpharm.2023.123748]
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. Zinan Zhang, Wenbin Cao, Huanchun Xing, Shuai Guo, Lijuan Huang, Lin Wang, Xin Sui, Kui Lu, Yuan Luo, Yongan Wang, Jun Yang.  (2023)  A mix & act liposomes of phospholipase A2-phosphatidylserine for acute brain detoxification by blood‒brain barrier selective-opening.  Acta Pharmaceutica Sinica B,      [PMID:38572103] [10.1016/j.apsb.2023.11.015]
5. Fanchang Wu, Mingjun Huang, Xue Zuo, Ruiye Xie, Jinman Liu, Junyu Ke, Weirong Li, Qi Wang, Yong Liang.  (2023)  Osthole/borneol thermosensitive gel via intranasal administration enhances intracerebral bioavailability to improve cognitive impairment in APP/PS1 transgenic mice.  Frontiers in Pharmacology,      [PMID:37521471] [10.3389/fphar.2023.1224856]
6. Zehao Wang, Ru Zhao, Hongfei Gao, Yang Yang, Xinyu Yang, Huiyan Gu, Lei Yang, Xiaonan Zhang, Tingting Liu.  (2023)  Solvent-free microwave extraction of essential oil and hydrosol from fresh leaves of Cinnamomum burmannii (Nees et T. Nees) Blume after screw extrusion treatment and evaluation of pancreatic lipase inhibitory activities in vitro compared to its main components.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2023.116983]
7. Xin Shen, Zhixiang Cui, Yidan Wei, Yingnan Huo, Duo Yu, Xin Zhang, Shirui Mao.  (2023)  Exploring the potential to enhance drug distribution in the brain subregion via intranasal delivery of nanoemulsion in combination with borneol as a guider.  Asian Journal of Pharmaceutical Sciences,      [PMID:38089837] [10.1016/j.ajps.2023.100778]
8. Liu Zhenyi, Wang Jing, Yin Meijuan, Liu Mengsheng, Gao Weijuan.  (2022)  Gas chromatography-mass spectrometry analysis of variations in the essential leaf oil of 6 Eucalyptus Species and allelopathy of mechanism 1,8-cineole.  CIENCIA RURAL,      [PMID:] [10.1590/0103-8478cr20210687]
9. Liu Zhen, Liu Kun.  (2022)  Reproducing ancient Chinese ink depending on gelatin/chitosan and modern experimental methodology.  Heritage Science,  10  (1): (1-12).  [PMID:] [10.1186/s40494-022-00739-w]
10. Huijuan Li, Xinghui Song, Huiru Li, Lifei Zhu, Shengbo Cao, Jifeng Liu.  (2022)  Sesquiterpenes and Monoterpenes from the Leaves and Stems of Illicium simonsii and Their Antibacterial Activity.  MOLECULES,  27  (3): (1115).  [PMID:35164380] [10.3390/molecules27031115]
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. 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]
13. Qun Ma, Manman Dai, Huimin Zhang, Luyu Bai, Ning He.  (2020)  Effect of different doses of borneol on the pharmacokinetics of vinpocetine in rat plasma and brain after intraocular administration.  XENOBIOTICA,      [PMID:31424307] [10.1080/00498254.2019.1658139]
14. Xiaocheng Fan, Li Yang, Ting Wang, Tiedong Sun, Shuting Lu.  (2019)  pH-responsive cellulose-based dual drug-loaded hydrogel for wound dressing.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2019.109290]
15. Lingwei Meng, Xiaoyang Chu, Haoyue Xing, Xuan Liu, Xin Xin, Liqing Chen, Mingji Jin, Youyan Guan, Wei Huang, Zhonggao Gao.  (2019)  Improving glioblastoma therapeutic outcomes via doxorubicin-loaded nanomicelles modified with borneol.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:31260781] [10.1016/j.ijpharm.2019.118485]
16. Yujia Zhang, Nan Zhang, Hui Song, He Li, Jin Wen, Xiaochuan Tan, Wensheng Zheng.  (2019)  Design, characterization and comparison of transdermal delivery of colchicine via borneol-chemically-modified and borneol-physically-modified ethosome.  DRUG DELIVERY,      [PMID:30744424] [10.1080/10717544.2018.1559258]
17. Xiaobang Liu, Jiaqun Du, Junpeng Sun, Han Wang, Jinyu An, Yingqiao Li, Yu Hu, Shuai Cheng, Huicong Feng, He Tian, Xifan Mei, Yang Qiu, Chao Wu.  (2024)  Borneol-Functionalized Macrophage Membrane-Encapsulated Mesoporous Selenium Nanoparticles Loaded with Resveratrol for the Treatment of Spinal Cord Injury.  ACS Applied Materials & Interfaces,      [PMID:39511843] [10.1021/acsami.4c12454]
18. He Rong-rong, Ma Chuan-rui, He Xin, Dong Yan-xi, Li Hui, Chu Zi-xuan, Yang Xi-he, Wang Jia-qi, Wang Ting, Wang Feng-qing, Du Fei-fei, Rao Ying, Yu Wen-xuan, Gao Xiu-mei, Fan Guan-wei, Cheng Chen, Li Chuan.  (2024)  Circulating metabolites of Borneolum syntheticum (Bingpian) ameliorate atherosclerosis in ApoE−/− mice via inhibiting macrophage foam-cell formation.  ACTA PHARMACOLOGICA SINICA,      [PMID:39472494] [10.1038/s41401-024-01406-5]
19. Long Yanqiu, Lei Fang, Hu Jie, Zheng Zhiyun, Gui Shuangying, He Ning.  (2024)  Design and Evaluation of Ophthalmic Thermosensitive In Situ Gel of Compound Salvia.  AAPS PHARMSCITECH,  25  (7): (1-19).  [PMID:39164556] [10.1208/s12249-024-02913-8]
20. Huanyan Liang, Feifei Lv, Mengting Xian, Chenghua Luo, Lei Zhang, Meihua Yang, Qian Li, Xiangsheng Zhao.  (2025)  Inhibition Mechanism of Cinnamomum burmannii Leaf Essential Oil Against Aspergillus flavus and Aflatoxins.  Foods,  14  (4): (682).  [PMID:40002124] [10.3390/foods14040682]
21. Guanlin Wang, Zizhao Zhai, Wenhao Wang, Xiao Xia, Haihua Guo, Xiao Yue, Xiaoyuan Wang, Bing Zhu, Zhengwei Huang, Xin Pan, Ying Huang, Chuanbin Wu, Xuejuan Zhang.  (2024)  Tailored Borneol-Modified Lipid Nanoparticles Nasal Spray for Enhanced Nose-to-Brain Delivery to Central Nervous System Diseases.  ACS Nano,      [PMID:39158142] [10.1021/acsnano.4c08279]
22. Yuhsien Lai, Xuesong Wu, Zhuoyu Jiang, Yifei Fang, Xiuting Liu, Dan Hong, Yanyun Jiang, Guozhen Tan, Shiqi Tang, Siyao Lu, David Wei, Sam T. Hwang, Kit S. Lam, Liangchun Wang, Yanyu Huang, Zhenrui Shi.  (2024)  Topical treatment of tyrosine kinase 2 inhibitor through borneol-embedded hydrogel: Evaluation for preventive, therapeutic, and Recurrent management of psoriasis.  Bioactive Materials,      [PMID:39104775] [10.1016/j.bioactmat.2024.07.013]
23. Xiangbin Sun, Yuanyuan Xie, Xiaobing Ma, Yufeng He, Pengfei Song, Rongmin Wang.  (2025)  Phosphonium Cationic Borneol Stereochemical Membrane Breaking Arrow: High Antibacterial and Antibiofilm Activity.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.5c00203]
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