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7647-10-1

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7647-10-1 Usage

Chemical Description

Different sources of media describe the Chemical Description of 7647-10-1 differently. You can refer to the following data:
1. Palladium chloride and lithium chloride are used in the preparation of [PdCl{1-(1-naphthyl)-1-methyl-p-allyl}].
2. Palladium chloride is a compound with the formula PdCl2.

Description

Palladium chloride is a commonly used precious metal catalysts, molecular formula is PaCl2, the appearance is brown-red needle-like crystals or powder, easily deliquescence, the relative density is 4.0 (18 ℃), melting point is 500 ℃ (decomposition), soluble in water, ethanol, acetone and hydrogen bromide. Decomposition in ammonia chloride, potassium iodide, ammonia solution, and precipitation of palladium. [Uses] (1)used as the analysis reagents, such as determination of trace palladium, mercury, thallium, iodine, etc. (2) palladium test strips is used to test carbon monoxide. (3) also used to search for cracks of buried underground gas pipeline cracks, study of agricultural plant resources, preparation of palladium catalyst, electroplating watch parts and photography, and so on. [Preparation method] by melting palladium dichloride hydrate, make it lost part of chloride to get Palladium chlorine finished products. Figure 1 the molecular structure of Palladium chloride.

Chemical Properties

Palladium chloride is a dark brown powder, hygroscopic (absorbs moisture from the air). It is incompatible with acids, aluminium, ammonia, magnesium, nitrates, zinc, heat, thiocyanates, and organic solvents. Thermal decomposition of palladium chloride may release chlorine, hydrogen chloride, and oxides of palladium. It is used as a catalyst, photographic, and electroplating reagent. Palladium and its alloys are used as catalysts in the (petro)chemical and, above all, in the automotive industries. Applications of palladium compounds for electronics and electrical technology include use in metallisation processes (thick film paste), electrical contacts and switching systems, in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar. Palladium chloride is a stable chemical substance and is incompatible with strong oxidising agents.

Physical properties

l Properties Red rhombohedral crystal; hygroscopic; density 4.0g/cm3; melts at 679°C; dissolves slowly in water; also soluble in ethanol and acetone; dissolves rapidly in hydrochloric acid.

Uses

Different sources of media describe the Uses of 7647-10-1 differently. You can refer to the following data:
1. suzuki reaction
2. Palladium(II) chloride(PdCl2) is a dark brown color and is used to coat other metals without the need for electrolysis. It is also used in photography, to make indelible inks, and as a catalyst in analytical chemistry (used to speed up or slow down chemical reactions).
3. Palladium chloride is used in photography; toning solutions; electroplating parts of docks and watches; detecting carbon monoxide leaks in buried gas pipes; manufacture of indelible ink; preparation of metal for use as a catalyst; catalyst in jewelry; in dental alloys.
4. Palladium dichloride is a starting material for preparing several palladium compounds. It also is used for detection of carbon monoxide. For such detection, a paper is soaked in very dilute solution of PdCl2 which is decolorized by CO, methane and other reducing substances. It also is used in toning and electroplating solutions and in photography for porcelain pictures.

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.

General Description

Dark brown crystals.

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

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  • 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

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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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