Palladium CAS#: 7440-05-3

By Janice Zhang,
Palladium-CAS-7440-05-3
IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

英文名Palladium
IUPAC Namepalladium
分子结构Palladium-CAS-7440-05-3
CAS编号 7440-05-3
EINECS Number231-115-6
MDL NumberMFCD03457879
别名palladium, palladium on carbon, palladium atom, palladium(0), palladium,, palladiun, Palladium; 7440-05-3; CAS Number 7440-05-3; CAS NO 7440-05-3
分子式Pd
分子量106.42
InChIInChI=1S/Pd
InChI KeyKDLHZDBZIXYQEI-UHFFFAOYSA-N
Canonical SMILES[Pd]
Patent Information
Patent IDTitlePublication Date
US2013/300039-[4-(3-CHLORO-2-FLUORO-PHENYLAMINO)-7-METHOXY-QUINAZOLINE-6-YLOXY]-1,4-DIAZA-SPIRO[5.5]UNDECANE-5-ONE DIMALEATE, USE THEREOF AS A MEDICAMENT AND METHOD FOR THE PRODUCTION THEREOF2013
US2013/79412Branched 3-phenylpropionic acid derivatives and their use2013
US2013/851286-(4-HYDROXY-PHENYL)-3-ALKYL-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIC ACID AMIDE DERIVATIVES AS KINASE INHIBITORS2013

Physical Data

AppearanceWet black powder
Melting Point1,554.69 °C (2,830.44 °F)
Resistivity9.96 μΩ-cm, 20°C
Boiling Point, °C Pressure (Boiling Point), Torr
2200750
2540750
3000 – 3300750
3980750
Density, g·cm-3Measurement Temperature, °C
12.053527.2
1219.85
11.9920
Refractive IndexWavelength (Refractive Index), nmComment (Refractive Index)
1.65 – 3.4600depending on the thickness of Pd layer
1.62579

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Temperature (NMR Spectroscopy), °C Comment (NMR Spectroscopy)
Spectrum2Dneat (no solvent, solid phase)
SpectrumothersolidSignals given
Spectrum, Linewidth of NMR absorption105Pdsolid matrix-268.95 – 26.85
Description (IR Spectroscopy)Solvent (IR Spectroscopy)Comment (IR Spectroscopy)
Bandsneat (no solvent, solid phase)500 cm**-1 – 4000 cm**-1
Spectrumneat (no solvent, solid phase) 1900 cm**-1 – 2200 cm**-1
Spectrumneat (no solvent, solid phase) 690 cm**-1 – 4000 cm**-1
Description (UV/VIS Spectroscopy)Solvent (UV/VIS Spectroscopy)Comment (UV/VIS Spectroscopy)
Spectrum, Band assignmentwater600 nm – 1500 nm
Spectrum, Band assignmentethane-1,2-diol250 nm – 550 nm
Spectrumsolid400 nm – 1000 nm
Spectrum, Band assignmentisopropyl alcohol200 nm – 1200 nm
Spectrum, Band assignmentdimethylformamide450 nm – 750 nm

Route of Synthesis (ROS)

Route of Synthesis (ROS) of Palladium CAS 7440-05-3
ConditionsYield
With hydrazine hydrate In methanol cellulose (5 g) added to soln. of PdCl2 (0.443 g) in MeOH; stirred (15 min); 80% hydrazine hydrate added dropwise (15 min); stirred (12 h, room temp.); solid filtered; washed with methanol and acetone; dried (vac.);99%
With hydrogenchloride; hydrazine In water98%
With formic acid In not given refluxing a soln. of PdCl2 and HCOOH for 30 min; decantation, washing with water, drying for 2 h at 120°C;96%
With perchloric acid; 2,4-dichlorophenol; phosphododecatungstate In water Kinetics; Irradiation (UV/VIS); irradiated (>320 nm) at pH 1 (HClO4) at 18.3°C for 150 min; ppt. collected, dried, elem. anal.;83%
With 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclo-hexadiene In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;

Toa THFsuspension (5.0 mL) of 89 mg (0.50 mmol) of brownpalladium (II) chloride prepared in a Schlenk tube under an argonatmosphere was added 141mg (0.50 mmol) of Me4BTDP in THF The solution (5.0 mL) was added dropwise at room temperature.It quickly became a black suspension.After 12 hours, stirring was stopped and the mixture was allowed to stand to precipitate a black solid.The brown supernatant was filtered off and the resulting precipitate was washed three times with 5.0 mL of THF.The solid after washing was dried to obtain 27 mg of black palladium powder (0.25 mmol, yield 50%).
50%

Safety and Hazards

Pictogram(s)flameexclamation-mark
SignalDanger
GHS Hazard StatementsH228: Flammable solid [Danger Flammable solids]
H315: Causes skin irritation [Warning Skin corrosion/irritation]
H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
H413: May cause long lasting harmful effects to aquatic life [Hazardous to the aquatic environment, long-term hazard]
Information may vary between notifications depending on impurities, additives, and other factors.
Precautionary Statement Codes P210, P240, P241, P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goods
Under the room temperature and away from light
HS Code381512
StorageUnder the room temperature and away from light
Shelf Life2 years
Market PriceUSD 2390/kg
Use Pattern
The product can be used as catalyst for;
• hydrogenation of alkenes, alkynes, ketones, nitriles, imines, azides, nitro groups, benzenoid and heterocyclic aromatics;
• hydrogenolysis of cyclopropanes, benzyl derivatives, epoxides, hydrazines, and halides;
• dehydrogenate aromatics and deformylate aldehydes.
Catalyst for:
• Stille reaction
• Hydrogenation reactions
• Suzuki-Miyaura cross-coupling and Heck-Mizoroki reactions
• Deoxygenation
• Oxidation reactions
• Coupling reactions

Ruthenium CAS#: 7440-18-8

By Janice Zhang,
Ruthenium-CAS-7440-18-8
IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

英文名Ruthenium
IUPAC Nameruthenium
分子结构Ruthenium-CAS-7440-18-8
CAS编号 7440-18-8
EINECS Number231-127-1
MDL NumberMFCD00011207
别名ruthenium, rhuthenium, ruthenium,, Rutenium, Ru, Rh, Ruthenium; CAS Number 7440-18-8; CAS NO 7440-18-8
分子式[Ru]
分子量101.07
InChIInChI=1S/Ru
InChI KeyKJTLSVCANCCWHF-UHFFFAOYSA-N
Canonical SMILES[Ru]
Patent Information
Patent IDTitlePublication Date
US2014/121400PROMOTED RUTHENIUM CATALYST FOR THE IMPROVED HYDROGENATION OF CARBOXYLIC ACIDS TO THE CORRESPONDING ALCOHOLS 2014
WO2009/53446NOVEL PREGABALIN INTERMEDIATES AND PROCESS FOR PREPARING THEM AND PREGABALIN 2009
WO2008/69984PRODUCTION OF BUTENES AND DERIVATIVES THEREFORM FROM DRY ETHANOL2008

Physical Data

AppearanceWet black powder
Melting Point2310 °C (lit.)
Boiling Point3900 °C(lit.)
Flash Point207.324°C
Density12.45 g/ml
Description (Adsorption (MCS)) Partner (Adsorption (MCS))
Adsorption to title compoundCO and H
Adsorption to title compoundcarbon monoxide
Adsorption to title compoundmethanol
Adsorption to title compoundCO
Adsorption to title compoundchlorine

Spectra

Description (IR Spectroscopy)Solvent (IR Spectroscopy)Temperature (IR Spectroscopy), °CComment (IR Spectroscopy)
Spectrumneat (no solvent, solid phase)1000 cm**-1 – 3000 cm**-1
Spectrumneat (no solvent)256.851900 cm**-1 – 2200 cm**-1
Spectrumneat (no solvent, solid phase)2800 cm**-1 – 4000 cm**-1
Description (UV/VIS Spectroscopy)Solvent (UV/VIS Spectroscopy)Comment (UV/VIS Spectroscopy)
Spectrum, Band assignmentethane-1,2-diol200 nm – 800 nm
Spectrum, Band assignmentsolid0.5 eV – 6.5 eV
Spectrum, Band assignmentneat (no solvent)260 nm – 380 nm

Route of Synthesis (ROS)

Route of Synthesis (ROS) of Ruthenium CAS 7440-18-8
ConditionsYield
With carbon monoxide In neat (no solvent) passing CO over RuO2, heating;
In neat (no solvent) heating at 1400 °C, cooling;
With hydrogen at 200℃; for 4h; α-aluminium oxide;

Experimental Procedure
300 g of a used catalyst comprising 2percent by weight of RuO2 on α-aluminum oxide as support was reduced in a stream of hydrogen at 200° C. in a rotary tube furnace for 3 hours. Here, the catalyst was firstly heated to 200° C. in a stream of nitrogen, and was then reduced in a stream of N2/H2 (5:1) for 1 hour and subsequently in pure H2 for 3 hours. The reduced catalyst was dispensed under a nitrogen atmosphere into a vessel into which nitrogen was passed. The reduced catalyst was subsequently transferred under a nitrogen atmosphere into a 2000 ml stirred apparatus and 1160 g of 32percent strength by weight hydrochloric acid were added. While stirring and introducing nitrogen, the mixture was heated to 100° C. The mixture was subsequently stirred at 100° C. while sparging the solution with 50 l/h of air for 24 hours. A dark red ruthenium chloride solution was obtained and this was decanted off from the residue. The support which remained as residue was washed with about 1 l of water until neutral. The support was subsequently dried at 120° C. for 16 hours and the ruthenium content of the support was determined. The determination indicated a ruthenium content of 0.20percent by weight. In comparison, the used catalyst comprised 1.49percent by weight of ruthenium. Thus, about 13percent of the originally comprised ruthenium remained on the support.
With CO In neat (no solvent) passing CO over RuO2, heating;
In neat (no solvent) heating at 1400 °C, cooling;;
With H2 In neat (no solvent) reduction of RuO2 in hydrogen at 873 K within 2 h;
With H2 In neat (no solvent) reduction of RuO2 (commercial compound or prepared from RuCl3 by calcining in air) in flowing H2 (1.7 cm**3/s) at temps. between 553 and 803 K; degassing at react. temp. for 3 h down to 1.33E-4 Pa;
In neat (no solvent) RuO2 decompd. into metal at temp. of about 100°C at heating rate 1°C/min under Ar/H2; detn. by TG anal.;

Safety and Hazards

Pictogram(s)flame
SignalWarning
GHS Hazard StatementsH228: Flammable solid [Danger Flammable solids]
H413: May cause long lasting harmful effects to aquatic life [Hazardous to the aquatic environment, long-term hazard]
Information may vary between notifications depending on impurities, additives, and other factors. 
Precautionary Statement CodesP210, P240, P241, P273, P280, P370+P378, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goods
Under the room temperature and away from light
HS Code381512
StorageUnder the room temperature and away from light
Shelf Life1 year
Market PriceUSD 790/kg
Use Pattern
catalyst for producing monofunctionalized dialkylphosphinic acids, esters or salts
manufacturing a hydrocarbon
enantioselective preparation of herbicide metolachlor precursor (S)-2-ethyl-N-(1-methoxypropan-2-yl)-6-methylaniline
Ruthenium is mostly used in effective hardener
catalyst for fluoroolefins hydrogenation
metallic element for hydrodenitrogenation catalyst
Catalyst useful for N-demethylation and/or N-acylation of N-methylated heterocycle