Isoborneol - ≥90%(GC) , CAS No.124-76-5

CAS: 124-76-5 Cat. No.: I138125 Fórmula: C10H18O Peso molecular: 154.25 Beilstein Registry Number: 6(2)80 Número EC: 204-712-4
Disponible para pedir
GRADE & PURITY ≥90%(GC)
Synonyms
CAS-124-76-5 | CHEBI:141542 | ethyl butyl amine | Exoborneol | SCHEMBL115722 | UNII-L88RA8N5EG | (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2alpha-ol | 2-Camphanol, exo- | A828291 | Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel- | ISOBORNEO
Storage
Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
5g
I138125-5g
—
3 Disponible

8,59€

12,93€
Guardar 4,34 € (33.56%)
25g
I138125-25g
—
3 Disponible

12,06€

18,14€
Guardar 6,07 € (33.49%)
100g
I138125-100g
—
3 Disponible

24,21€

36,36€
Guardar 12,15 € (33.41%)
500g
I138125-500g
—
2 Disponible

65,86€

98,84€
Guardar 32,97 € (33.36%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥90%(GC) 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Used as a synthetic flavor, as a moth repellent, cold sore topical medication, muscle liniment, and steam-inhaled cough suppressant. It is also used in Used in perfumes.

Specifications

Sinónimos
CAS-124-76-5 | CHEBI:141542 | ethyl butyl amine | Exoborneol | SCHEMBL115722 | UNII-L88RA8N5EG | (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2alpha-ol | 2-Camphanol, exo- | A828291 | Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel- | ISOBORNEO
Especificaciones y pureza
≥90%(GC)
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥90%(GC)
Nombres e identificadores
Pubchem Sid504764031
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764031
Sonrisas canónicasCC1(C2CCC1(C(C2)O)C)C
IUPAC Name(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
InChIKeyDTGKSKDOIYIVQL-MRTMQBJTSA-N
INCHI1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1
Isómeros SMILES C[C@@]12CC[C@@H](C1(C)C)C[C@H]2O
WGK Alemania 2
RTECS NP7300000
Peso molecular 154.25
Beilstein 6(2)80
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
ClasePrenol 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
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 Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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
H2209360Certificate of AnalysisFeb 04, 2026 I138125
H2209366Certificate of AnalysisFeb 04, 2026 I138125
H2209367Certificate of AnalysisFeb 04, 2026 I138125
H2209369Certificate of AnalysisFeb 04, 2026 I138125
A2619146Certificate of AnalysisJan 26, 2026 I138125
H1611030Certificate of AnalysisOct 14, 2025 I138125
L2427168Certificate of AnalysisDec 31, 2024 I138125
Propiedades químicas y físicas
SolubilidadInsoluble in water. Soluble in dipropylene glycol, ethyl alcohol (1gm. in 2ml. 70% alcohol).
Punto de inflamación (°F)199.4 °F
Punto de inflamación (°C)93 °C
Punto de fusión (°C)212-214 °C
Peso molecular154.250 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 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. 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. Xiaoming Zeng, Hao He, Liejiang Yuan, Haizhi Wu, Cong Zhou.  (2024)  Determination of 24 Trace Aromatic Substances in Rosemary Hydrosol by Dispersed Liquid–Liquid Microextraction–Gas Chromatography.  Processes,  12  (3): (498).  [PMID:] [10.3390/pr12030498]
3. Miao Liang, Runhu Xin, Wei Guan, Yuping Liu.  (2024)  Effect of moisture loss on aroma profile, key odorants, and fatty acids of Amomum tsaoko during vacuum oven drying.  FOOD CHEMISTRY,      [PMID:39674017] [10.1016/j.foodchem.2024.142421]
4. Yan Yang, Siying Liu, Yan Wang, Qin Yang, Baoan Wang, Yuting Zhang, Zaikang Tong, Junhong Zhang.  (2025)  Antifungal mechanisms of Phoebe bournei wood essential oil against Botryosphaeria dothidea and its application in apples.  POSTHARVEST BIOLOGY AND TECHNOLOGY,      [PMID:] [10.1016/j.postharvbio.2025.113703]
5. Shijie Xu, Ying Li, Xingsheng Wan, Mingen Fei, Wendi Liu, Renhui Qiu.  (2026)  Sustainable 4D printing of bio-based shape memory polymer composites derived from isoborneol–thioctic acid with photothermal actuation.  COMPOSITES COMMUNICATIONS,      [PMID:] [10.1016/j.coco.2026.102807]
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