(-)-Linalool - ≥95%, sum of enantiomers , CAS No.126-91-0

CAS: 126-91-0 Cat. No.: L302318 Molecular Weight: 154.25 EC Number: 204-811-2
AVAILABLE TO ORDER
GRADE & PURITY ≥95% sum of enantiomers
Synonyms
Spectrum2_001944 | (R)-3,7-dimethylocta-1,6-dien-3-ol | CHEBI:28 | SPECTRUM1501212 | BSPBio_002785 | Spectrum_000212 | (-)-Linalool | SCHEMBL891312 | (-)-Linalool, analytical standard | BPBio1_000150 | Spectrum5_000393 | KBioSS_000692 | KBio2_000692 | KBi
Storage
Protected from light,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
L302318-5g
5
$16.90
25g
L302318-25g
4
$52.90
100g
L302318-100g
2
$150.90
500g
L302318-500g
3
$555.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥95%, sum of enantiomers for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,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.

Overview

product description:

(-)-Linalool is a monoterpene compound mainly found in many essential oils. It shows anti-nociceptive and anti-inflammatory activity.


application:

(-)-Linalool can be used as a reactant in:The enantioselective preparation of ophiobolin sesterterpene via diastereoselective reductive radical cascade cyclization.The total synthesis of (-)-5,6-dihydrocineromycin B via (-)-linalool O-triethylsilyl ether.The total synthesis of pladienolide B analog.

Specifications

Synonyms
Spectrum2_001944 | (R)-3, 7-dimethylocta-1, 6-dien-3-ol | CHEBI:28 | SPECTRUM1501212 | BSPBio_002785 | Spectrum_000212 | (-)-Linalool | SCHEMBL891312 | (-)-Linalool, analytical standard | BPBio1_000150 | Spectrum5_000393 | KBioSS_000692 | KBio2_000692 | KBi
Specifications & Purity
≥95%, sum of enantiomers
Storage
Protected from light, Room temperature
Shipped In
Normal
Action Type
ACTIVATOR
Purity
≥95%
Names and Identifiers
Pubchem Sid488189804
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189804
Canonical SmilesCC(=CCCC(C)(C=C)O)C
IUPAC Name(3R)-3,7-dimethylocta-1,6-dien-3-ol
InChIKeyCDOSHBSSFJOMGT-JTQLQIEISA-N
INCHI1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1
Isomeric SMILES CC(=CCC[C@](C)(C=C)O)C
WGK Germany 3
RTECS RG5800000
Molecular Weight 154.25
Reaxy-Rn 1362385
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1362385&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 ParentAcyclic monoterpenoids
Alternative Parents Tertiary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Acyclic monoterpenoid - Tertiary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle.
External Descriptors Acyclic monoterpenoids
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
rep Replicase polyprotein 1ab (378 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.

14 results found

Lot NumberCertificate TypeDateItem
F2303455Certificate of AnalysisMar 13, 2026 L302318
F2303460Certificate of AnalysisMar 13, 2026 L302318
F2303500Certificate of AnalysisMar 13, 2026 L302318
F2303501Certificate of AnalysisMar 13, 2026 L302318
F2303502Certificate of AnalysisMar 13, 2026 L302318
F2303503Certificate of AnalysisMar 13, 2026 L302318
F2303510Certificate of AnalysisMar 13, 2026 L302318
E2312248Certificate of AnalysisFeb 04, 2026 L302318
L2107541Certificate of AnalysisSep 13, 2024 L302318
L2107542Certificate of AnalysisSep 13, 2024 L302318
I2128282Certificate of AnalysisJul 12, 2024 L302318
I2128283Certificate of AnalysisJul 12, 2024 L302318
I2128284Certificate of AnalysisJul 12, 2024 L302318
I2128285Certificate of AnalysisJul 12, 2024 L302318

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Chemical and Physical Properties
SensitivityLight sensitive
Freezing Point(°C)−18±3°, neat
Refractive Index1.462
Flash Point(°F)168.8 °F
Flash Point(°C)76 °C
Boil Point(°C)198.5°C
Molecular Weight154.250 g/mol
XLogP32.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count4
Exact Mass154.136 Da
Monoisotopic Mass154.136 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity154.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
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
References
1. Jianjun Cheng, Qinghua Chen, Qianshuang Guo, Yongjun Du.  (2022)  Moth sex pheromones affect interspecific competition among sympatric species and possibly population distribution by modulating pre-mating behavior.  Insect Science,  30  (2): (501-516).  [PMID:35900899] [10.1111/1744-7917.13099]
2. Zhang Hongfei, Li Weizheng, Luo Qianwen, Yang Lei, Gong Dongfeng, Teng Xiaohui, Guo Xianru, Yuan Guohui.  (2018)  Fatal Attraction: Ricinus communis Provides an Attractive but Risky Mating Site for Holotrichia parallela Beetles.  JOURNAL OF CHEMICAL ECOLOGY,  44  (10): (965-974).  [PMID:30116996] [10.1007/s10886-018-0994-5]
3. Han Yan, Wei-Xuan Li, Ying-Lin Zhu, Zhi-Yuan Lin, Dan Chen, Yue Zhang, Hai-Peng Lv, Wei-Dong Dai, De-Jiang Ni, Zhi Lin, Yin Zhu.  (2024)  Comprehensive comparison of aroma profiles and chiral free and glycosidically bound volatiles in Fujian and Yunnan white teas.  FOOD CHEMISTRY,      [PMID:38547713] [10.1016/j.foodchem.2024.139067]
4. Yue Chen, Linbo Gou, Di Liu, Shengfang Wu, Xiuwen Zhou, Tai-Ping Fan, Long Wang, Yujie Cai.  (2025)  Engineering an ATP-saving mevalonate pathway for high-efficiency S-(+)-linalool production in Serratia marcescens.  Synthetic and Systems Biotechnology,      [PMID:] [10.1016/j.synbio.2025.11.010]
5. Jiarui Tong, Xiangrong Zhu, Xiumei Chen, Nengguo Tao.  (2026)  Trans-2-hexenal-loaded gelatin/dialdehyde starch/nanocellulose cushioning aerogel: synergistic postharvest preservation of Chinese bayberry with 1-MCP.  FOOD RESEARCH INTERNATIONAL,      [PMID:41794491] [10.1016/j.foodres.2026.118612]
Solution Calculators
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