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α-Terpineol - >80.0%(GC,sum of isomers), high purity , CAS No.98-55-5

    Grade & Purity:
  • ≥80%(GC)
  • mixture of isomers
In stock
Item Number
A151627
Grouped product items
SKU Size
Availability
Price Qty
A151627-25ml
25ml
3
$18.90
A151627-100ml
100ml
4
$64.90
A151627-500ml
500ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$292.90

Basic Description

Synonyms CHEBI:22469 | 1-Menthene-8-ol | CAS-8000-41-7 | D70165 | ALPHA-TERPINEOL [FCC] | DSSTox_GSID_40775 | ALPHA-TERPINEOL [HSDB] | 3-Cyclohexene-1-methanol, .alpha.,.alpha.4-trimethyl- | PC 593 | TERPIN MONOHYDRATE IMPURITY A [EP IMPURITY] | UNII-21334LVV8W |
Specifications & Purity ≥80%(GC), mixture of isomers
Shipped In Normal
Product Description

α-Terpineol is a monoterpene alcohol. It is one of the components responsible for the antifungal activity in Melaleuca alternifolia (tea tree) essential oil.[1] The reaction rate constant of α-terpineol with the OH radical and ozone was found to be (1.9±0.5)×10-10cm3 molecule-1s-1 and (3.0±0.2)×10-16cm3 molecule-1s-1, respectively.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Prenol lipids
Subclass Monoterpenoids
Intermediate Tree Nodes Not available
Direct Parent Menthane monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Tertiary alcohols  Hydrocarbon derivatives  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Tertiary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
Description This 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 a monoterpenol

Associated Targets(Human)

DGAT1 Tclin Diacylglycerol O-acyltransferase 1 (1719 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB1 Tclin Adrenergic receptor beta (1214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gardnerella vaginalis (35 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gabrg2 GABA-A receptor; alpha-1/beta-2/gamma-2 (554 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Smooth muscle of trachea (74 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488182345
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182345
IUPAC Name 2-(4-methylcyclohex-3-en-1-yl)propan-2-ol
INCHI InChI=1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3
InChIKey WUOACPNHFRMFPN-UHFFFAOYSA-N
Smiles CC1=CCC(CC1)C(C)(C)O
Isomeric SMILES CC1=CCC(CC1)C(C)(C)O
RTECS WZ6700000
Molecular Weight 154.25
Beilstein 6(4)251
Reaxy-Rn 1906604
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1906604&ln=

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.

7 results found

Lot Number Certificate Type Date Item
H1714079 Certificate of Analysis Mar 04, 2025 A151627
F1920210 Certificate of Analysis Apr 12, 2023 A151627
H2219119 Certificate of Analysis Jul 23, 2022 A151627
H2219410 Certificate of Analysis Jul 23, 2022 A151627
B2314046 Certificate of Analysis Jul 23, 2022 A151627
H2219117 Certificate of Analysis Jul 23, 2022 A151627
C2307584 Certificate of Analysis Aug 12, 2021 A151627

Chemical and Physical Properties

Solubility Solubility in water: Practically Insoluble; Degree of Solubility in water: 1,980 mg/l 20 °C; Very soluble in Ether,Alcohol
Refractive Index 1.483
Flash Point(°F) 194°F
Flash Point(°C) 90℃
Boil Point(°C) 210-219℃
Melt Point(°C) 31-32℃
Molecular Weight 154.250 g/mol
XLogP3 1.800
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 1
Exact Mass 154.136 Da
Monoisotopic Mass 154.136 Da
Topological Polar Surface Area 20.200 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 168.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

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