Tetrakis(triphenylphosphine)paladium(0) CAS 14221-01-3 Assay >99,0% Pd >9,2%

Katrangan singkat:

Jeneng: Tetrakis (triphenylphosphine) paladium (0)

Sinonim: Pd(PPh3)4;Pd-Tetrakis

CAS: 14221-01-3

Assay:> 99.0%

Pd: >9,2%

Penampilan: Bubuk kuning

E-Mail: alvin@ruifuchem.com

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Tag produk

katrangan:

Shanghai Ruifu Chemical Co., Ltd. is the leading supplier of Tetrakis(triphenylphosphine)palladium(0) (CAS: 14221-01-3) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Sifat Kimia:

Jeneng Kimia	Tetrakis(triphenylphosphine)paladium(0)
sinonim	Pd(PPh3)4;Palladium-tetrakis (triphenylphosphine);Pd-Tetrakis
Nomer CAS	14221-01-3
Nomer CAT	RF-PI2207
Status Simpenan	Ing Simpenan, Skala Produksi Nganti Ton
Formula Molekul	C72H60P4Pd
Bobot Molekul	1155.56
Simpen Ing Gas Inert	Simpen Ing Gas Inert
Sensitif	Sensitif Udara, Sensitif Panas
Kelarutan banyu	Ora larut ing banyu
Kelarutan ing Toluene	Larut ing 1% Toluene, Meh Transparansi
Merk	Kimia Ruifu

Spesifikasi:

Item	Spesifikasi
Penampilan	Bubuk Kuning
Assay (Analisis Unsur)	>99,0% Palladium (Pd): >9,2%
Ag	<0,0003%
Au	<0,0003%
Pt	<0,0003%
Rh	<0,0003%
Ir	<0,0003%
Fe	<0,003%
Al	<0,0003%
Pb	<0,00015%
Ni	<0,00015%
Cu	<0,00015%
Si	<0,0003%
Sn	<0,00015%
Titik Lebur	103.0~105.0 ℃
Pengujian Kotoran Oksida	<0,60%
ICP	Konfirmasi Komponen Pd lan P Dikonfirmasi
Spektrum 1H NMR	Conforms kanggo Struktur
Test Standar	Standar Perusahaan

Paket & Panyimpenan:

Paket: Botol, tas Aluminium foil, 25kg / Karton Drum, utawa miturut kabutuhan pelanggan

Kondisi panyimpenan:Simpen ing wadhah sing disegel ing papan sing adhem lan garing;Nglindhungi saka cahya lan Kelembapan

Kaluwihan:

FAQ:

Aplikasi:

Tetrakis(triphenylphosphine)paladium(0) (CAS: 14221-01-3) akeh digunakake minangka katalis kanggo reaksi kopling katalis paladium.Katalis sing ngasilake dhuwur digunakake ing reaksi kopling.Tetrakis(triphenylphosphine)paladium(0) akeh digunakake minangka katalis kanggo reaksi kopling katalis paladium.Aplikasi sing misuwur kalebu reaksi Heck, kopling Suzuki, kopling Stille, kopling Sonogashira, lan kopling Negishi.Katalis kanggo kopling Suzuki ester organoboronik sekunder kiral.Reaksi SNAr sing dikatalisis Palladium kanggo sintesis eter heteroaril.Katalis kanggo kopling silang senyawa a-diazokarbonil karo asam arilboronik.Sintesis diastereoselektif trans-1,2-diazetidines.Siklisasi ion alkynyl iminium katalis Palladium.Reagen sing akeh digunakake ing macem-macem transformasi kalebu Heck arylation, enyne lan diyne cycloisomerization.Katalis kanggo cross-coupling.Iku senyawa palladium penting, digunakake digunakake ing catalysis kimia lan industri electroplating, minangka bahan baku utama saka palladium plating, punika jinis anyar saka electroplating uyah utama, efficiency electroplating dhuwur, resik lan lingkungan pangayoman, wis digunakake digunakake ing industri elektronik.