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7647-10-1

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7647-10-1 Usage

Chemical Description

Palladium chloride and lithium chloride are used in the preparation of [PdCl{1-(1-naphthyl)-1-methyl-p-allyl}].

Chemical Description

Palladium chloride is a compound with the formula PdCl2.

Description

Palladium chloride, with the molecular formula PdCl2, is a dark brown crystalline compound. It appears as brown-red needle-like crystals or powder and is hygroscopic, meaning it absorbs moisture from the air. The relative density of palladium chloride is 4.0, and it has a melting point of 500°C (decomposition). It is soluble in water, ethanol, acetone, and hydrogen bromide, and decomposes in ammonia chloride, potassium iodide, ammonia solution, and precipitation of palladium.

Uses

1. Analytical Chemistry: Palladium chloride is used as an analysis reagent for the determination of trace amounts of palladium, mercury, thallium, iodine, and other elements.
2. Carbon Monoxide Detection: Palladium test strips are used to detect carbon monoxide, as they change color when exposed to the gas.
3. Gas Pipeline Crack Detection: It is used to search for cracks in buried underground gas pipelines.
4. Agricultural Plant Resource Study: Palladium chloride aids in the study of agricultural plant resources.
5. Catalyst Preparation: It is used in the preparation of palladium catalysts.
6. Electroplating: Palladium chloride is used for electroplating watch parts and other metals without the need for electrolysis.
7. Photography: It is utilized in the photography industry for toning solutions and porcelain pictures.
8. Indelible Ink: Palladium chloride is used in the manufacture of indelible ink.
9. Suzuki Reaction: It serves as a catalyst in the Suzuki reaction, an important carbon-carbon bond-forming process in organic chemistry.
Used in Automotive Industry:
Palladium and its alloys are used as catalysts in the automotive industry, particularly for catalytic converters.
Used in Electronics and Electrical Technology:
Palladium compounds are used in metallization processes (thick film paste), electrical contacts, switching systems, and the synthesis of semiconducting metal-containing polymers.
Physical Properties:
Palladium chloride forms red rhombohedral crystals and has a density of 4.0 g/cm3. It melts at 679°C and dissolves slowly in water, as well as in ethanol and acetone. It dissolves rapidly in hydrochloric acid.
Chemical Properties:
Palladium chloride is a stable chemical substance that is incompatible with strong oxidizing agents, acids, aluminum, ammonia, magnesium, nitrates, zinc, heat, thiocyanates, and organic solvents. Thermal decomposition may release chlorine, hydrogen chloride, and oxides of palladium.

Production Methods

The palladium powder is added to the reactor containing hydrochloric acid, with stirring, passing the air, an oxidation reaction is performed, generating palladium chloride solution, the solution is purified, filtered, concentrated by evaporation, cooling and crystallization, centrifugal separation, and dried to obtain a palladium chloride finished products. Pd+2HCl+0.5O2→PdCl2+H2O

Preparation

Palladium dichloride is prepared by dissolving palladium metal in aqua regia or hydrochloric acid in the presence of chlorine. Alternatively, it may be prepared by heating palladium sponge with chlorine gas at 500°C.

Reactions

Palladium dichloride dissolves in HCl forming tetrachloropalladate ion, PdCl2+2Clˉ→ [PdCl4]2ˉ The complex ion catalyzes various types of organic reactions including oxidation of ethylene to acetaldehyde in aqueous solution (the Wacker Process): PdCl42ˉ+ C2H4 + H2O → CH3CHO + Pd + 2HCl + 2Clˉ Palladium dichloride forms polymeric carbonyl complexes when the dry chloride is heated in a stream of carbon monoxide charged with methane vapor. Such complexes include [PdCl2(CO)n] and [PdCl(CO)2]n. The reaction also occurs in aqueous phase resulting in decolorization of the solution. When H2S is passed through palladium dichloride solution, it yields a brown-black precipitate of palladium monosulfide, PdS. When heated with sulfur at 450 to 500°C, palladium dichloride forms palladium disulfide, PdS2, a grey-black crystalline compound, insoluble in strong acids but soluble in aqua regia, and which converts to monosulfide, PdS, on heating at 600°C. When ammonia gas is passed through an aqueous solution of PdCl2, the product is tetrammine palladium(II) chloride, Pd(NH4)2Cl2. The same product also is obtained in dry state by passing ammonia gas over anhydrous PdCl2.

Reactivity Profile

Palladium chloride is a weak oxidizing agent. Palladium chloride is reduced in solution by hydrogen or carbon monoxide to metallic palladium. . Decomposed at high temperatures to metallic palladium and chlorine.

Fire Hazard

Flash point data for Palladium chloride are not available. Palladium chloride is probably combustible.

Safety Profile

Poison by intraperitoneat, intravenous, and intratracheal routes. Moderately toxic by ingestion. Experimental reproductive effects. A skin irritant. Questionable carcinogen with experimental carcinogenic data. Human mutation data reported. When heated to decomposition it emits highly toxic fumes of Cl-. See also PALLADIUM

Purification Methods

The anhydrous salt is insoluble in H2O and dissolves in HCl with difficulty. The dihydrate forms red hygroscopic crystals that are readily reduced to Pd. Dissolve it in conc HCl through which dry Cl2 is bubbled. Filter this solution which contains H2PdCl4 and H2PdCl6 and on evaporation it yields a residue of pure PdCl2. [Grube in Handbook of Preparative Inorganic Chemistry (Ed Brauer) Academic Press Vol II p 1582 1965, Mozingo Org Synth Coll Vol III 685 1955.]

Check Digit Verification of cas no

The CAS Registry Mumber 7647-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7647-10:
(6*7)+(5*6)+(4*4)+(3*7)+(2*1)+(1*0)=111
111 % 10 = 1
So 7647-10-1 is a valid CAS Registry Number.
InChI:InChI=1/2ClH.2H2O.Pd/h2*1H;2*1H2;/q;;;;+2/p-2

7647-10-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (11034)  Palladium(II) chloride, 99.9% (metals basis), Pd 59.0% min   

  • 7647-10-1

  • 0.5g

  • 393.0CNY

  • Detail
  • Alfa Aesar

  • (11034)  Palladium(II) chloride, 99.9% (metals basis), Pd 59.0% min   

  • 7647-10-1

  • 2g

  • 1442.0CNY

  • Detail
  • Alfa Aesar

  • (11034)  Palladium(II) chloride, 99.9% (metals basis), Pd 59.0% min   

  • 7647-10-1

  • 10g

  • 5406.0CNY

  • Detail
  • Alfa Aesar

  • (11034)  Palladium(II) chloride, 99.9% (metals basis), Pd 59.0% min   

  • 7647-10-1

  • 50g

  • 22797.0CNY

  • Detail
  • Alfa Aesar

  • (43085)  Palladium(II) chloride, Premion?, 99.999% (metals basis), Pd 59.5% min   

  • 7647-10-1

  • 1g

  • 1002.0CNY

  • Detail
  • Alfa Aesar

  • (43085)  Palladium(II) chloride, Premion?, 99.999% (metals basis), Pd 59.5% min   

  • 7647-10-1

  • 5g

  • 3806.0CNY

  • Detail
  • Alfa Aesar

  • (43085)  Palladium(II) chloride, Premion?, 99.999% (metals basis), Pd 59.5% min   

  • 7647-10-1

  • 25g

  • 13757.0CNY

  • Detail
  • Alfa Aesar

  • (40019)  Palladium(II) chloride, solution, Pd 20-25% w/w (cont. Pd)   

  • 7647-10-1

  • (c)1g

  • 1348.0CNY

  • Detail
  • Alfa Aesar

  • (40019)  Palladium(II) chloride, solution, Pd 20-25% w/w (cont. Pd)   

  • 7647-10-1

  • (c)5g

  • 3652.0CNY

  • Detail
  • Alfa Aesar

  • (12623)  Palladium(II) chloride, solution, Pd 9.0-11.0% w/w (cont. Pd)   

  • 7647-10-1

  • (c)1g

  • 1196.0CNY

  • Detail
  • Alfa Aesar

  • (12623)  Palladium(II) chloride, solution, Pd 9.0-11.0% w/w (cont. Pd)   

  • 7647-10-1

  • (c)5g

  • 4381.0CNY

  • Detail
  • Aldrich

  • (323373)  Palladium(II)chloride  99.999%

  • 7647-10-1

  • 323373-1G

  • 1,422.72CNY

  • Detail

7647-10-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name palladium(II) chloride

1.2 Other means of identification

Product number -
Other names Palladium(II) Chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7647-10-1 SDS

7647-10-1Synthetic route

N,N,N,N,-tetramethylethylenediamine
110-18-9

N,N,N,N,-tetramethylethylenediamine

palladium(II) chloride
7647-10-1

palladium(II) chloride

N,N,N',N'-tetramethylethylenediamine palladium(II) chloride
14267-08-4

N,N,N',N'-tetramethylethylenediamine palladium(II) chloride

Conditions
ConditionsYield
In acetonitrile refluxing PdCl2-acetonitrile solution; cooling to 20°C; adding tmeda; analysis;90%
N,N,N'N'-tetramethyl-1,3-propanediamine
110-95-2

N,N,N'N'-tetramethyl-1,3-propanediamine

palladium(II) chloride
7647-10-1

palladium(II) chloride

dichlor(N,N,N',N'-tetramethyl-1,3-propanediamine)palladium(II)
21363-94-0

dichlor(N,N,N',N'-tetramethyl-1,3-propanediamine)palladium(II)

Conditions
ConditionsYield
In acetonitrile refluxing PdCl2-acetonitrile solution; cooling to 20°C; adding tmpda; analysis;90%
4-but-2-enyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester

4-but-2-enyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester

palladium(II) chloride
7647-10-1

palladium(II) chloride

4-(3-oxo-butyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester

4-(3-oxo-butyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester

Conditions
ConditionsYield
copper(I) chloride In water; N,N-dimethyl-formamide71%
copper(II) chloride dihydrate

copper(II) chloride dihydrate

4-allylazetidin-2-one
68485-52-9

4-allylazetidin-2-one

palladium(II) chloride
7647-10-1

palladium(II) chloride

sodium hydrogencarbonate
144-55-8

sodium hydrogencarbonate

4-(2-oxo-propyl)-azetidin-2-one
68485-90-5

4-(2-oxo-propyl)-azetidin-2-one

Conditions
ConditionsYield
mercury(II) diacetate In methanol; ethyl acetate70%
mercury(II) diacetate In methanol; ethyl acetate70%
4-bromo-1,3-benzenedicarboxylic acid dimethyl ester
28730-78-1

4-bromo-1,3-benzenedicarboxylic acid dimethyl ester

para-fluorostyrene
405-99-2

para-fluorostyrene

palladium(II) chloride
7647-10-1

palladium(II) chloride

A

methyl 4-[2-4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate

methyl 4-[2-4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate

B

(2S)-2-{2-(4-fluorophenethyl)-5-[1-(4-fluorophenyl)-2-(imidazol-1-yl)ethylaminomethyl]benzoylamino}-4-methylsulfanylbutyric acid

(2S)-2-{2-(4-fluorophenethyl)-5-[1-(4-fluorophenyl)-2-(imidazol-1-yl)ethylaminomethyl]benzoylamino}-4-methylsulfanylbutyric acid

Conditions
ConditionsYield
With tributyl-amine In dichloromethane; water
4-bromo-1,3-benzenedicarboxylic acid dimethyl ester
28730-78-1

4-bromo-1,3-benzenedicarboxylic acid dimethyl ester

para-fluorostyrene
405-99-2

para-fluorostyrene

palladium(II) chloride
7647-10-1

palladium(II) chloride

methyl 4-[2-(4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate

methyl 4-[2-(4-fluorophenyl)ethenyl]-3-methoxycarbonylbenzoate

Conditions
ConditionsYield
With tributyl-amine In dichloromethane; water
1-bromo-4-methoxy-benzene
104-92-7

1-bromo-4-methoxy-benzene

palladium(II) chloride
7647-10-1

palladium(II) chloride

potassium carbonate
584-08-7

potassium carbonate

acrylic acid
79-10-7

acrylic acid

3-(4'-methoxyphenyl)propenoic acid
830-09-1

3-(4'-methoxyphenyl)propenoic acid

Conditions
ConditionsYield
In water
6-fluoro-3-nitroaniline
369-36-8

6-fluoro-3-nitroaniline

palladium(II) chloride
7647-10-1

palladium(II) chloride

2,4-Dinitrofluorobenzene
70-34-8

2,4-Dinitrofluorobenzene

4-Fluoro-3-nitroaniline
364-76-1

4-Fluoro-3-nitroaniline

Conditions
ConditionsYield
In palladium dichloride
cupric chloride

cupric chloride

C2 H5 O(C2 H4 O)18 C2 H5

C2 H5 O(C2 H4 O)18 C2 H5

1,11-dodecadiene
5876-87-9

1,11-dodecadiene

palladium(II) chloride
7647-10-1

palladium(II) chloride

A

1-dodecen-11-one
5009-33-6

1-dodecen-11-one

B

2,11-dodecadione
7029-09-6

2,11-dodecadione

Conditions
ConditionsYield
In water
cupric chloride

cupric chloride

C2 H5 O(C2 H4 O)18 CH3

C2 H5 O(C2 H4 O)18 CH3

6-methyl-1,5-heptadiene
7270-50-0

6-methyl-1,5-heptadiene

palladium(II) chloride
7647-10-1

palladium(II) chloride

6-Methyl-hept-5-en-2-on
110-93-0

6-Methyl-hept-5-en-2-on

Conditions
ConditionsYield
In water
furfural
98-01-1

furfural

palladium(II) chloride
7647-10-1

palladium(II) chloride

N-(3-chloro-4-(3-fluorobenzyloxy)phenyl)-6-iodoquinazolin-4-amine
231278-20-9

N-(3-chloro-4-(3-fluorobenzyloxy)phenyl)-6-iodoquinazolin-4-amine

5-(4-[3-chloro-4-(3-fluorobenzyloxy)-anilino]-6-quinazolinyl)-furan-2-carbaldehyde 4-methylbenzenesulfonate

5-(4-[3-chloro-4-(3-fluorobenzyloxy)-anilino]-6-quinazolinyl)-furan-2-carbaldehyde 4-methylbenzenesulfonate

Conditions
ConditionsYield
With N2; potassium acetate In 1,2-dimethoxyethane; water; N,N-dimethyl-formamide2.5 g (55%)
1,1'-bis(diphenylphosphino) ferrocene

1,1'-bis(diphenylphosphino) ferrocene

palladium(II) chloride
7647-10-1

palladium(II) chloride

2-(4-{2-[2-(4-bromophenyl)-5-methyloxazol-4-yl]ethoxy}phenoxy)-2-methylpropionic acid ethyl ester
328918-90-7

2-(4-{2-[2-(4-bromophenyl)-5-methyloxazol-4-yl]ethoxy}phenoxy)-2-methylpropionic acid ethyl ester

phenylboronic acid
98-80-6

phenylboronic acid

2-[4-(2-{2-[4-(4-Benzoyl-phenoxy)-phenyl]-5-methyl-oxazol-4-yl}-ethoxy)-phenoxy]-2-methyl-propionic Acid

2-[4-(2-{2-[4-(4-Benzoyl-phenoxy)-phenyl]-5-methyl-oxazol-4-yl}-ethoxy)-phenoxy]-2-methyl-propionic Acid

Conditions
ConditionsYield
With sodium hydroxide; K2CO3; potassium iodide In ethanol; methoxybenzene
1-Heptene
592-76-7

1-Heptene

palladium(II) chloride
7647-10-1

palladium(II) chloride

2C5H11CHCH2*2PdCl2={C5H11CHCH2PdCl2}2

2C5H11CHCH2*2PdCl2={C5H11CHCH2PdCl2}2

Conditions
ConditionsYield
In tetrahydrofuran Pd-compd. and 1-heptene (1.4 molar ratio) in THF stirred at room temp. for 30 min.;

7647-10-1Upstream product

7647-10-1Relevant articles and documents

Method for preparing of L-phenylephrine hydrochloride

-

, (2008/06/13)

The present invention relates to an improved process for preparing L-phenylephrine hydrochloride 3 on an industrial scale by asymmetric hydrogenation as the key step and a special sequence of subsequent steps, using [Rh(COD)Cl]2 as catalyst and a chiral, two-pronged phosphine ligand such as (2R,4R)-4-(dicyclohexylphosphino)-2-(diphenylphosphino-methyl)-N-methyl-aminocarbonyl-pyrrolidine as the catalyst system.

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