Bis(tri-tert-butylphosphine)palladium(0) - Pd 20.8% , CAS No.53199-31-8

CAS: 53199-31-8 Cat. No.: B110179 Molecular Weight: 511.05 EC Number: 640-284-9
AVAILABLE TO ORDER
GRADE & PURITY Pd 20.8%
Synonyms
Fu catalyst | Pd(t-Bu3P)2 | BIS(TRI-T-BUTYLPHOSPHINE)PALLADIUM | Palladium, bis[tris(1,1-dimethylethyl)phosphine]- | PB42990 | palladium;tritert-butylphosphane | DTXSID80370359 | Bis[tris(tert-butyl)phosphine]palladium | STR08646 | MFCD03094580 | SC10403
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
B110179-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$28.90
1g
B110179-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$97.90
5g
B110179-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$428.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Pd 20.8% 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Product class

M-P, Homogeneous Catalysts, M-C, Alkyl Ligands, Monodentate Ligands


Reaction type

Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Carbonylation, Mizoroki Heck Coupling Reaction, Negishi Coupling Reaction, Stille Reaction, Suzuki-Miyaura Coupling Reaction


Chemical properties

Chemical formula

C24H54P2Pd

Empirical formula

[Pd(P(tBu3))2]

Molecular weight

511.06

Metal

Pd

Theoretical metal content

21

Physical state

crystalline

Color

white

Applications & references

Diastereoselctive synthesis of isochromans using a Palladium catalyzed carboiodination.


Reference: Org. Lett. 2012, 14, 4806. (DOI: 10.1021/ol302111y)


High yielding Palladium catalyzed C-H arylation of electron-enriched heteroarenes with aryl halides.


Reference: J. Org. Chem. 2010, 75, 6998. (DOI: 10.1021/jo101433g)


Arylation of hydrosiloxanes for the synthesis of symmetrical and unsymmetrical siloxanes. They are interesting substrates for the usage as liquid crystals, starting materials for cross coupling reactions and biologically active compounds.


Reference: Chem. Comm. 2013, 49, 11275. (DOI: 10.1039/c3cc46294c)



Specifications

Synonyms
Fu catalyst | Pd(t-Bu3P)2 | BIS(TRI-T-BUTYLPHOSPHINE)PALLADIUM | Palladium, bis[tris(1, 1-dimethylethyl)phosphine]- | PB42990 | palladium;tritert-butylphosphane | DTXSID80370359 | Bis[tris(tert-butyl)phosphine]palladium | STR08646 | MFCD03094580 | SC10403
Specifications & Purity
Pd 20.8%
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesCC(C)(C)P(C(C)(C)C)C(C)(C)C.CC(C)(C)P(C(C)(C)C)C(C)(C)C.[Pd]
IUPAC Namepalladium;tritert-butylphosphane
InChIKeyMXQOYLRVSVOCQT-UHFFFAOYSA-N
INCHI1S/2C12H27P.Pd/c2*1-10(2,3)13(11(4,5)6)12(7,8)9;/h2*1-9H3;
Isomeric SMILES CC(C)(C)P(C(C)(C)C)C(C)(C)C.CC(C)(C)P(C(C)(C)C)C(C)(C)C.[Pd]
WGK Germany 3
Molecular Weight 511.05
Reaxy-Rn 14300595
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14300595&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
SuperclassOrganophosphorus compounds
ClassOrganic phosphines and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentOrganic phosphines and derivatives
Alternative Parents Organic transition metal salts  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkNot available
Substituents Phosphine - Organic transition metal salt - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as organic phosphines and derivatives. These are organic compounds containing a phosphine derivative, with the general formula B1P(R2)R3 (R1-R3=alkyl, aryl).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

10 results found

Lot NumberCertificate TypeDateItem
E2627252Certificate of AnalysisMay 22, 2026 B110179
E2627255Certificate of AnalysisMay 22, 2026 B110179
E2627275Certificate of AnalysisMay 22, 2026 B110179
A2615039Certificate of AnalysisJun 28, 2025 B110179
H2529194Certificate of AnalysisJun 28, 2025 B110179
H2529197Certificate of AnalysisJun 28, 2025 B110179
I2509909Certificate of AnalysisJun 28, 2025 B110179
I2113010Certificate of AnalysisJun 16, 2023 B110179
I2113009Certificate of AnalysisJun 16, 2023 B110179
G1901008Certificate of AnalysisFeb 03, 2023 B110179
Chemical and Physical Properties
SolubilitySoluble in toluene benzene, slight soluble in chloroform and acetone. Decomposes in water.
Sensitivityair & heat & light & moisture sensitive
Melt Point(°C)>300°C
Molecular Weight511.100 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count6
Exact Mass510.274 Da
Monoisotopic Mass510.274 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count27
Formal Charge0
Complexity128.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Solution Calculators
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