Geranylgeraniol - ≥95% , CAS No.24034-73-9

CAS: 24034-73-9 Cat. No.: G132893 Summenformel: C20H34O Molekulargewicht: 290.483 EG-Nummer: 623-656-5
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GRADE & PURITY ≥95%
Synonyms
all trans-3,7,11-15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol | Tetraprenol | Trans,Trans,Trans-Geranylgeraniol | Geranylgeraniol (Natural) | BCP25724 | FLUOROLINK(R) D | trans,trans,trans-Geranylgeraniol | 3,7,11,15-tetramethylhexadeca-2E,6E,10E,14-tetr
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Size
Deutschland (EU)
USA*
Price
Qty
20mg
G132893-20mg
—
2 Auf Lager
34,62€
100mg
G132893-100mg
—
2 Auf Lager
101,44€
500mg
G132893-500mg
—
2 Auf Lager
336,60€
1g
G132893-1g
—
2 Auf Lager
392,13€
5g
G132893-5g
—
2 Auf Lager
1.550,56€
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at -20°C,Argon charged 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.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. This compound has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro When working with statins, geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. It has been found to induce apoptosis in HL-60 cells.
An intermediate in the mevalonate pathway.

Specifications

Synonyme
all trans-3,7,11-15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol | Tetraprenol | Trans,Trans,Trans-Geranylgeraniol | Geranylgeraniol (Natural) | BCP25724 | FLUOROLINK(R) D | trans,trans,trans-Geranylgeraniol | 3,7,11,15-tetramethylhexadeca-2E,6E,10E,14-tetr
Spezifikationen & Reinheit
≥95%
Biochemische und physiologische Mechanismen
As the pyrophosphate, the metabolic precursor of all diterpenes. Screening in vitro shows this to be a potent and selective agent against Mycobacterium tuberculosis.Mevalonate pathway intermediate and geranylgeranylpyrophosphate precursor. Prevents bone r
Storage
Store at -20°C,Argon charged
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Hinweis
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Reinheit
≥95%
Namen und Kennungen
Pubchem Sid504763351
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504763351
Kanonisches LächelnCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C
IUPAC Name(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ol
InChIKeyOJISWRZIEWCUBN-QIRCYJPOSA-N
INCHI1S/C20H34O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h9,11,13,15,21H,6-8,10,12,14,16H2,1-5H3/b18-11+,19-13+,20-15+
Isomere SMILES CC(=CCC/C(=C/CC/C(=C/CC/C(=C/CO)/C)/C)/C)C
Molekulargewicht 290.483
Reaxy-Rn 1797446
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1797446&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
KlassePrenol lipids
SubclassDiterpenoids
Intermediate Tree Nodes Not available
Direct ParentAcyclic diterpenoids
Alternative Parents Long-chain fatty alcohols  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Acyclic diterpenoid - Long chain fatty alcohol - Fatty alcohol - Fatty acyl - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.
External Descriptors Acyclic diterpenoids
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DGAT1 Tclin Diacylglycerol O-acyltransferase 1 (1719 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus mutans (2687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 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
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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 NumberCertificate TypeDatumArtikel
B23011087Certificate of AnalysisAug 13, 2026 G132893
B23011056Certificate of AnalysisAug 13, 2026 G132893
B23011003Certificate of AnalysisAug 13, 2026 G132893
B2301844Certificate of AnalysisAug 13, 2026 G132893
B23011005Certificate of AnalysisAug 03, 2026 G132893
B23011086Certificate of AnalysisAug 03, 2026 G132893
C2507186Certificate of AnalysisMar 20, 2025 G132893
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in DMSO (>25 mg/ml), ethanol (>25 mg/ml), chloroform, dichloromethane, ethyl acetate, hexane, ether, and acetone.
Molekulargewicht290.500 g/mol
XLogP36.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count10
Exact Mass290.261 Da
Monoisotopic Mass290.261 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count21
Formal Charge0
Complexity390.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count3
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds3
Covalently-Bonded Unit Count1
Citations of This Product
Referenzen
1. Haichun Zeng, Jiatong Zeng, Beilin Meng, Yuxin Zhou, Kai Zhou, Li Rao.  (2025)  A Novel Sesquiterpene Synthase from Neophaeococcomyces mojaviensis for α-Santalene Production.  ACS Synthetic Biology,      [PMID:41258727] [10.1021/acssynbio.5c00559]
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