α-Terpineol - ≥98% , CAS No.10482-56-1

CAS: 10482-56-1 Cat. No.: T111437 Molecular Weight: 154.25 Beilstein Registry Number: 2325137 EC Number: 233-986-8
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(S)-2-(4-methylcyclohex-3-en-1-yl)propan-2-ol | (S)-alpha-terpineol | (-)-.alpha.-Terpineol | 3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, (1S)- | alpha-Terpinenol | (1S)-alpha,alpha,4-trimethyl-3-cyclohexene-1-methanol | (S)-(-)-Terpineol | 3-Cycl
Storage
Room temperature,Argon charged,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
10ml
T111437-10ml
2
$9.90
50ml
T111437-50ml
3
$27.90
100ml
T111437-100ml
2
$39.90
250ml
T111437-250ml
3
$79.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature,Argon charged,Cool Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 52 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

α-Citronellol can be used to synthesize α-citronellol esters of acetic acid and acetic anhydride through an esterification reaction mediated by lipases. 

α-Citronellol is a type of monoterpene alcohol. It is one of the antifungal active components in the essential oil of the inter-leaf white mulberry (tea tree). The reaction rate constants of α-citronellol with OH free radicals and ozone are (1.9 ± 0.5) × 10-10 cm3 molecule-1 s-1 and (3.0 ± 0.2) × 10-16 cm3 molecule-1 s-1, respectively.

Specifications

Synonyms
(S)-2-(4-methylcyclohex-3-en-1-yl)propan-2-ol | (S)-alpha-terpineol | (-)-.alpha.-Terpineol | 3-Cyclohexene-1-methanol, alpha, alpha, 4-trimethyl-, (1S)- | alpha-Terpinenol | (1S)-alpha, alpha, 4-trimethyl-3-cyclohexene-1-methanol | (S)-(-)-Terpineol | 3-Cycl
Specifications & Purity
≥98%
Storage
Room temperature, Argon charged, Cool
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid504758794
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758794
Canonical SmilesCC1=CCC(CC1)C(C)(C)O
IUPAC Name2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-ol
InChIKeyWUOACPNHFRMFPN-SECBINFHSA-N
INCHI1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1
Isomeric SMILES CC1=CC[C@H](CC1)C(C)(C)O
WGK Germany 2
RTECS WZ6700000
Alternate CAS 98-55-5
Molecular Weight 154.25
Beilstein 2325137
Reaxy-Rn 1906604
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1906604&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 ParentMenthane monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Tertiary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Tertiary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
DescriptionThis 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 Menthane monoterpenoids - Cyclic monoterpenes
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella aerogenes (4963 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus mutans (2687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus flavus (8875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cyberlindnera jadinii (900 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Corynebacterium ammoniagenes (75 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cutibacterium acnes (887 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Penicillium chrysogenum (1593 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Musca domestica (713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tetranychus urticae (2600 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rdl GABA receptor subunit (76 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leptinotarsa decemlineata (1161 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Malassezia furfur (70 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Psoroptes ovis (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Corticium (78 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.

29 results found

Lot NumberCertificate TypeDateItem
F2603671Certificate of AnalysisMay 14, 2026 T111437
F2603595Certificate of AnalysisMay 14, 2026 T111437
F2603594Certificate of AnalysisMay 14, 2026 T111437
F2603593Certificate of AnalysisMay 14, 2026 T111437
F2603592Certificate of AnalysisMay 14, 2026 T111437
F2603487Certificate of AnalysisMay 14, 2026 T111437
C2611119Certificate of AnalysisMar 19, 2026 T111437
D2602557Certificate of AnalysisMar 19, 2026 T111437
E2218243Certificate of AnalysisMar 10, 2026 T111437
E2218093Certificate of AnalysisMar 10, 2026 T111437
K2120605Certificate of AnalysisSep 04, 2025 T111437
A2506173Certificate of AnalysisApr 26, 2024 T111437
C2301808Certificate of AnalysisNov 28, 2022 T111437
J2517207Certificate of AnalysisNov 28, 2022 T111437
I2423617Certificate of AnalysisNov 28, 2022 T111437
I2403004Certificate of AnalysisNov 28, 2022 T111437
H2429111Certificate of AnalysisNov 28, 2022 T111437
G2512036Certificate of AnalysisNov 28, 2022 T111437
B2507195Certificate of AnalysisNov 28, 2022 T111437
C2301807Certificate of AnalysisNov 28, 2022 T111437
D2515034Certificate of AnalysisNov 28, 2022 T111437
C2301809Certificate of AnalysisNov 28, 2022 T111437
C2301834Certificate of AnalysisNov 28, 2022 T111437
C2302389Certificate of AnalysisNov 28, 2022 T111437
F2417070Certificate of AnalysisNov 28, 2022 T111437
E2509007Certificate of AnalysisNov 28, 2022 T111437
D2402006Certificate of AnalysisNov 28, 2022 T111437
E2218100Certificate of AnalysisMar 26, 2022 T111437
E2218099Certificate of AnalysisMar 26, 2022 T111437

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Chemical and Physical Properties
Solubility1 part of terpineol can be dissolved in 2 parts (volume) of 70% ethanol solution, slightly soluble in water and glycerol.
SensitivityMoisture sensitive.
Refractive Index1.482
Flash Point(°F)194 °F
Flash Point(°C)90 °C
Boil Point(°C)217-218 °C
Melt Point(°C)31-35 °C
Molecular Weight154.250 g/mol
XLogP31.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass154.136 Da
Monoisotopic Mass154.136 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity168.000
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
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