(E)-Labd-13-ene-8,15-diol - ≥95% , CAS No.10267-31-9

Name: (E)-Labd-13-ene-8,15-diol - ≥95% , CAS No.10267-31-9
SKU: E345210
Availability: InStock

CAS: 10267-31-9 Cat. No.: E345210 Formula: C₂₀H₃₆O₂ Peso molecolare: 308.5

COA

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(E)-Labd-13-ene-8,15-diol - ≥95% CAS No(10267-31-9) by Aladdin Scientific

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Disponibile su ordine

GRADE & PURITY ≥95%

Synonyms

Labd-13(E)-ene-8α,15-diol | 13E-Labdene-8α,15-diol | Copal-8α,15-diol | [1R-[1a(E),2ß,4aß,8aa]]-Decahydro-1-(5-hydroxy-3-methyl-3-pentenyl)-2,5,5,8a-tetramethyl-2-naphthalenol | (1R,2R,4aS,8aS)-Decahydro-1-[(3E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8a-tet

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Calcolatori di soluzioni Recensioni

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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Labd-13(E)-ene-8α,15-diol is a diterpene with the labdane skeleton which can be extracted from Cistus symphytijbfolius.

Specifications

Sinonimi

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%

Nomi e identificatori

Pubchem Sid	504763856
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504763856
Sorrisi canonici	CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C
IUPAC Name	(1R,2R,4aS,8aS)-1-[(E)-5-hydroxy-3-methylpent-3-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
InChIKey	LEOHDQKUMQKLMP-NUKBDRAPSA-N
INCHI	1S/C20H36O2/c1-15(10-14-21)7-8-17-19(4)12-6-11-18(2,3)16(19)9-13-20(17,5)22/h10,16-17,21-22H,6-9,11-14H2,1-5H3/b15-10+/t16-,17+,19-,20+/m0/s1
Isomeri SMILES	C/C(=C\CO)/CC[C@@H]1[C@]2(CCCC([C@@H]2CC[C@@]1(C)O)(C)C)C
Peso molecolare	308.5
Reaxy-Rn	2561434
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2561434&ln=

Documentazione

📋 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 Diterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Classe	Prenol lipids
Subclass	Diterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Diterpenoids
Alternative Parents	Fatty alcohols Tertiary alcohols Cyclic alcohols and derivatives Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Diterpenoid - Labdane diterpenoid - Fatty alcohol - Fatty acyl - Tertiary alcohol - Cyclic alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
Descrizione	This compound belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.
External Descriptors	Not available
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

Struttura 3D

Obiettivi associati (umani)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

A498 (42825 Activities)

Lot Number	Certificate Type	Data	Oggetto
B2605156	Certificate of Analysis	Jan 31, 2026	E345210
B2605157	Certificate of Analysis	Jan 31, 2026	E345210
B2605158	Certificate of Analysis	Jan 31, 2026	E345210
K2229379	Certificate of Analysis	Sep 08, 2025	E345210
K2229392	Certificate of Analysis	Sep 08, 2025	E345210
K2229398	Certificate of Analysis	Sep 08, 2025	E345210
K2229403	Certificate of Analysis	Sep 08, 2025	E345210
E2512234	Certificate of Analysis	Apr 24, 2025	E345210
E2512235	Certificate of Analysis	Apr 24, 2025	E345210
E2512236	Certificate of Analysis	Apr 24, 2025	E345210
E2512247	Certificate of Analysis	Apr 24, 2025	E345210

Indice di rifrazione	n20D1.49 (Predicted)
Punto di ebollizione (°C)	~408.5° C at 760 mmHg (Predicted)
Punto di fusione (°C)	142.90° C (Predicted)
Peso molecolare	308.500 g/mol
XLogP3	5.100
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	4
Exact Mass	308.272 Da
Monoisotopic Mass	308.272 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	22
Formal Charge	0
Complexity	425.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

(E)-Labd-13-ene-8,15-diol - ≥95% , CAS No.10267-31-9

Why this grade

Storage & shipping

Quality documents

Literature proof

Panoramica

Specifications

Documentazione

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

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