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

COA COA
    Grade & Purity:
  • ≥95%
In stock
Item Number
E345210
Grouped product items
SKU Size
Availability
 Price Qty
E345210-5mg
5mg
3
$241.90
E345210-10mg
10mg
3
$344.90
E345210-25mg
25mg
2
$550.90
E345210-100mg
100mg
2
$1,374.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Half day flower family - diterpenes (1) Jinyeyan Rose (1) Plant terpenes (1)

Basic Description

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
Specifications & Purity ≥95%
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

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

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class 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
Description 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

Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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Hs-578T (29457 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
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IGROV-1 (47897 Activities)
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LOX IMVI (44321 Activities)
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MDA-MB-435 (38290 Activities)
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MDA-N (28205 Activities)
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Malme-3M (44254 Activities)
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Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
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Mus musculus (284745 Activities)
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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 504763856
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504763856
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
INCHI 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
InChIKey LEOHDQKUMQKLMP-NUKBDRAPSA-N
Smiles CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C
Isomeric SMILES C/C(=C\CO)/CC[C@@H]1[C@]2(CCCC([C@@H]2CC[C@@]1(C)O)(C)C)C
Molecular Weight 308.5
Reaxy-Rn 2561434
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2561434&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.

8 results found

Lot Number Certificate Type Date Item
E2512234 Certificate of Analysis Apr 24, 2025 E345210
E2512235 Certificate of Analysis Apr 24, 2025 E345210
E2512247 Certificate of Analysis Apr 24, 2025 E345210
E2512236 Certificate of Analysis Apr 24, 2025 E345210
K2229379 Certificate of Analysis Oct 10, 2022 E345210
K2229398 Certificate of Analysis Oct 10, 2022 E345210
K2229392 Certificate of Analysis Oct 10, 2022 E345210
K2229403 Certificate of Analysis Oct 10, 2022 E345210

Chemical and Physical Properties

Refractive Index n20D1.49 (Predicted)
Boil Point(°C) ~408.5° C at 760 mmHg (Predicted)
Melt Point(°C) 142.90° C (Predicted)
Molecular Weight 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 Ų
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

Solution Calculators

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