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Art. -Nr.: HY-W727466

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4,6-Dimethyldodecane

4,6-Dimethyldodecane is an alkane. 4,6-Dimethyldodecane can be derived from the oil of T. decandra. 4,6-Dimethyldodecane can be used in bacterial infection research.

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CAS. Nr.: 61141-72-8
Formel: C₁₄H₃₀
Molecular Weight:198.39

Speicherung:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (260 KB)

4,6-Dimethyldodecane Chemical Structure

CAS. Nr.: 61141-72-8

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Preis

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biologische Aktivität

Beschreibung

4,6-Dimethyldodecane is an alkane. 4,6-Dimethyldodecane can be derived from the oil of T. decandra. 4,6-Dimethyldodecane can be used in bacterial infection research^[1]^[2].

Chemical Information

CAS. Nr. 61141-72-8
Molecular Weight 198.39
Formel C₁₄H₃₀
SMILES

CCCCCCC(CC(CCC)C)C
Structure Classification
- Others
Initial Source
- Plants
- Labiatae
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

Protokoll

All Signal Pathway Related

Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (260 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Geethalakshmi R, et al. Evaluation of antimicrobial and antioxidant activity of essential oil of Trianthema decandra L. journal of pharmacy research, 2013, 6(1): 101-106.

[2]. Rubio-Sánchez R, et al. Feasibility of using volatile urine fingerprints for the differentiation of sexually transmitted infections. Appl Microbiol Biotechnol. 2023 Oct;107(20):6363-6376. [Content Brief]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Keywords

MOQ

Minimum order quantity

100 mg

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