Name: α-Terpineol - ≥98% , CAS No.10482-56-1
SKU: T111437
Availability: InStock

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

CAS: 10482-56-1 Cat. No.: T111437 Formule: C₁₀H₁₈O Poids moléculaire: 154.25 Beilstein Registry Number: 2325137 Numéro CE: 233-986-8

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α-Terpineol - ≥98% CAS No(10482-56-1) T111437 by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥98%

Synonyms

Storage

Room temperature,Argon charged

Shipped In

Normal

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Citations of This Product Calculateurs de solution Avis

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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 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.

Vue d’ensemble

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

Synonymes

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

Pubchem Sid

504758794

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504758794

Sourires canoniques

CC1=CCC(CC1)C(C)(C)O

IUPAC Name

2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-ol

InChIKey

WUOACPNHFRMFPN-SECBINFHSA-N

INCHI

1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1

Isomères SMILES

CC1=CC[C@H](CC1)C(C)(C)O

WGK Allemagne

RTECS

WZ6700000

CAS alternatif

98-55-5

Poids moléculaire

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

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Classe Prenol lipids
    - Subclass Monoterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Classe	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	Menthane monoterpenoids - Cyclic monoterpenes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)

Discover Target: UGT1A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)

Discover Target: UGT1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Pseudomonas aeruginosa (123386 Activities)

Lot Number	Certificate Type	Date	Article
F2603671	Certificate of Analysis	May 14, 2026	T111437
F2603595	Certificate of Analysis	May 14, 2026	T111437
F2603594	Certificate of Analysis	May 14, 2026	T111437
F2603593	Certificate of Analysis	May 14, 2026	T111437
F2603592	Certificate of Analysis	May 14, 2026	T111437
F2603487	Certificate of Analysis	May 14, 2026	T111437
C2611119	Certificate of Analysis	Mar 19, 2026	T111437
D2602557	Certificate of Analysis	Mar 19, 2026	T111437
E2218243	Certificate of Analysis	Mar 10, 2026	T111437
E2218093	Certificate of Analysis	Mar 10, 2026	T111437
K2120605	Certificate of Analysis	Sep 04, 2025	T111437
A2506173	Certificate of Analysis	Apr 26, 2024	T111437
C2301808	Certificate of Analysis	Nov 28, 2022	T111437
J2517207	Certificate of Analysis	Nov 28, 2022	T111437
I2423617	Certificate of Analysis	Nov 28, 2022	T111437
I2403004	Certificate of Analysis	Nov 28, 2022	T111437
H2429111	Certificate of Analysis	Nov 28, 2022	T111437
G2512036	Certificate of Analysis	Nov 28, 2022	T111437
B2507195	Certificate of Analysis	Nov 28, 2022	T111437
C2301807	Certificate of Analysis	Nov 28, 2022	T111437
D2515034	Certificate of Analysis	Nov 28, 2022	T111437
C2301809	Certificate of Analysis	Nov 28, 2022	T111437
C2301834	Certificate of Analysis	Nov 28, 2022	T111437
C2302389	Certificate of Analysis	Nov 28, 2022	T111437
F2417070	Certificate of Analysis	Nov 28, 2022	T111437
E2509007	Certificate of Analysis	Nov 28, 2022	T111437
D2402006	Certificate of Analysis	Nov 28, 2022	T111437
E2218100	Certificate of Analysis	Mar 26, 2022	T111437
E2218099	Certificate of Analysis	Mar 26, 2022	T111437

Solubilité	1 part of terpineol can be dissolved in 2 parts (volume) of 70% ethanol solution, slightly soluble in water and glycerol.
Sensibilité	Moisture sensitive.
Indice de réfraction	1.482
Point d'éclair (°F)	194 °F
Point d'éclair (°C)	90 °C
Point d'ébullition (°C)	217-218 °C
Point de fusion (°C)	31-35 °C
Poids moléculaire	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 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	168.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations by Application

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