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Tributylhexylphosphonium Bromide - >98.0%(T), high purity , CAS No.105890-71-9

    Grade & Purity:
  • ≥98%(T)
In stock
Item Number
T405095
Grouped product items
SKU Size
Availability
Price Qty
T405095-1g
1g
3
$10.90
T405095-5g
5g
2
$33.90
T405095-25g
25g
2
$113.90
T405095-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$374.90

Basic Description

Synonyms SCHEMBL1517962 | Tributyl(hexyl)phosphonium bromide | CS-0196427 | Tributyl(hexyl)phosphoniumbromide | NSC41947 | NSC-41947 | MFCD00134170 | T3840 | Tributylhexylphosphonium Bromide | E82322 | tributyl(hexyl)phosphanium;bromide | Phosphonium, tributylhexy
Specifications & Purity ≥98%(T)
Storage Temp Argon charged

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organophosphorus compounds
Class Tetraalkylphosphonium compounds
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Tetraalkylphosphonium compounds
Alternative Parents Organic bromide salts  Hydrocarbon derivatives  Organic cations  
Molecular Framework Aliphatic acyclic compounds
Substituents Tetraalkylphosphonium compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organic cation - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as tetraalkylphosphonium compounds. These are organophosphorus compounds that contain a tetravalent phosphorus atom substituted to four alkyl chains.
External Descriptors Not available

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella aerogenes (4963 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Enterococcus faecium (13803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

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 504769278
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504769278
IUPAC Name tributyl(hexyl)phosphanium;bromide
INCHI InChI=1S/C18H40P.BrH/c1-5-9-13-14-18-19(15-10-6-2,16-11-7-3)17-12-8-4;/h5-18H2,1-4H3;1H/q+1;/p-1
InChIKey ZBZFETNHIRABGK-UHFFFAOYSA-M
Smiles CCCCCC[P+](CCCC)(CCCC)CCCC.[Br-]
Isomeric SMILES CCCCCC[P+](CCCC)(CCCC)CCCC.[Br-]
PubChem CID 22712793
Molecular Weight 367.4
Reaxy-Rn 10315043

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.

4 results found

Lot Number Certificate Type Date Item
I2216533 Certificate of Analysis Jun 16, 2025 T405095
I2216638 Certificate of Analysis Jun 10, 2025 T405095
I2216626 Certificate of Analysis Jun 10, 2025 T405095
I2216637 Certificate of Analysis Jun 10, 2025 T405095

Chemical and Physical Properties

Sensitivity Hygroscopic
Molecular Weight 367.400 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 14
Exact Mass 366.205 Da
Monoisotopic Mass 366.205 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 155.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
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 2

Solution Calculators

Reviews

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