DIMETHYLPHENYLPHOSPHINE supplier

Name
DIMETHYLPHENYLPHOSPHINE
EINECS 211-595-3
CAS No. 672-66-2
Article Data55
CAS DataBase
Density 0.971 g/mL at 25 °C(lit.)
Solubility Insoluble in water
Melting Point 126-127ºC
Formula C8H11 P
Boiling Point 74-75 °C12 mm Hg(lit.)
Molecular Weight 138.149
Flash Point 122 °F
Transport Information UN 1993 3
Appearance Colorless to light yellow liquid
Safety Explodes when heated above 55°C or on impact. When heated to decomposition it emits acrid smoke and fumes. See also PEROXIDES, INORGANIC; PEROXIDES, ORGANIC.
Risk Codes 10-36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Dimethylphenylphosphine;NSC 158474; Phenyldimethylphosphine
PSA 13.59000
LogP 2.05340

Synthetic route

: dimethylphenylphosphine-borane complex

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With methanol; 4 A molecular sieve In tetrahydrofuran at 100℃; for 22h;	100%
With piperazinomethyl polystyrene resin In toluene at 115℃; for 17h;

: {Cp(PMe2Ph)2molybdenum(III) dichloride}

: 594-09-2
trimethylphosphane

: cyclopentadienylmolybdenum(III)(PMe3)2Cl2

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In toluene mixing of the Mo compd. with the free phosphine (molar ratio 2.2:1) in toluene;;	A 100% B n/a

...Expand

: 10311-08-7
dimethyl(phenyl)phosphine oxide

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With polymethylhydrosiloxane In neat (no solvent) at 150℃; for 10h; Reagent/catalyst; Temperature; Inert atmosphere; Green chemistry;	95%
With phenylsilane In neat (no solvent) at 110℃; for 1.75h; Reagent/catalyst; Temperature; Time; Inert atmosphere; Green chemistry;	95%
With [AlH3(triethylamine)] In hexane at 20℃; for 0.166667h; Inert atmosphere; Schlenk technique;	98 %Chromat.
With hexylsilane; trifluorormethanesulfonic acid In toluene at 70℃; for 24h; Inert atmosphere; Sealed tube; chemoselective reaction;	94 %Spectr.
With methanesulfonic acid; 1,1,3,3-Tetramethyldisiloxane In toluene at 100℃; for 4.5h; Inert atmosphere; Schlenk technique;

: (η-C5H5)2W(CH3)(CH2P(CH3)2C6H5)PF6

A: (tungsten(η-cyclopentadienyl)2(ethylene)H)(PF6)

B: 82917-98-4
(C5H5)2W(CH2P(CH3)2C6H5)(C2H5)(1+)*PF6(1-)

C: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
heated in sealed tube for 12 d at 75°C; elem. anal.;	A n/a B 86% C n/a

...Expand

: 71844-81-0
[(C5H5)(C5H4)Zr(P(CH3)2C6H5)]2

A: 1291-32-3
zirconocene dichloride

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With hydrogenchloride In benzene-d6 (N2); HCl gas added to complex soln. at 0°C, shaken at room temp.; not isolated, detected by NMR;	A 60% B 80%

: 917-64-6
methyl magnesium iodide

: 644-97-3
Dichlorophenylphosphine

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
	75%
With diethyl ether

: chlorodimethyloxobis(dimethylphenylphosphine)rhenium(V)

: 23936-60-9
1,2-bis(dimethylphosphanyl)ethane

: chlorodimethyloxo(bis(dimethylphosphino)ethane)rhenium(V)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In toluene byproducts: pyridine; N2 or Ar atmosphere of vac.; stirring (1 h); filtn., concn. (vac.), cooling (-20°C); elem. anal.;	A 62% B n/a

...Expand

: chlorodimethyloxobis(dimethylphenylphosphine)rhenium(V)

: 544-97-8
dimethyl zinc(II)

: trimethyloxo(dimethylphenylphosphine)rhenium(V)

B: 672-66-2
Dimethyl(phenyl)phosphine

C: 5158-46-3
methylzinc chloride

Conditions

Conditions	Yield
In toluene N2 or Ar atmosphere of vac.; 0°C; removal of solvent (0°C, vac.), extn. (pentane), removal of pentane (vac.);	A 51% B n/a C n/a

...Expand

: 366-18-7
[2,2]bipyridinyl

: chlorodimethyloxobis(dimethylphenylphosphine)rhenium(V)

: 544-97-8
dimethyl zinc(II)

: trimethyloxo(bipyridine)rhenium(V)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In toluene N2 or Ar atmosphere of vac.; addn. of soln. of ZnMe2 to soln. of Re-compd. in toluene (0°C), removal of solvent (0°C, vac.), extn. (pentane), addn. of bipy; removal of solvent and excess of bipy (vac.), crystn. (pentane, -50°C);	A 35% B n/a

...Expand

: 544-97-8
dimethyl zinc(II)

: 644-97-3
Dichlorophenylphosphine

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With benzene

: 24151-41-5
Dimethyl-phenyl-phosphonium

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With methane; trimethylphosphane at 47℃; under 0.01 Torr; Equilibrium constant; Thermodynamic data; irradiation with short electron pulse; ΔG;

: 2129-85-3
dimethyldiphenylphosphonium bromide

A: 672-66-2
Dimethyl(phenyl)phosphine

B: 1486-28-8
diphenyl(methyl)phosphine

Conditions

Conditions	Yield
In methanol; acetonitrile at 20℃; Product distribution; cathodic reduction, influence of potential on the product ratio;

: 594-09-2
trimethylphosphane

A: 672-66-2
Dimethyl(phenyl)phosphine

B Mo2Cl4(PMe2Ph)3(PMe3): Mo2Cl4(PMe2Ph)3(PMe3)

Conditions

Conditions	Yield
With Mo2Cl4(PMe2Ph)4 In (2)H8-toluene Thermodynamic data; ΔH(excit.); ΔS(excit.);

: 7732-18-5
water

: dichloro-phenyl-phosphine; compound with dimethylphenylphosphine

A: 7647-01-0
hydrogenchloride

B: 1779-48-2
phenylphosphinic acid

C: 672-66-2
Dimethyl(phenyl)phosphine

...Expand

: 462-06-6
fluorobenzene

: 26464-99-3
dimethyl(trimethylsilyl)phosphine

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In benzene-d6 at 180℃; for 90h;	60 % Spectr.

: C8H11P*H(1+)*BF4(1-)

: 6372-44-7
(dibutyl)(phenyl)phosphine

A: C14H23P*BF4(1-)*H(1+)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In dichloromethane-d2 at 20℃; Equilibrium constant;

...Expand

: C8H11P*H(1+)*BF4(1-)

: 6372-42-5
cyclohexyldiphenylphosphine

A: C18H21P*H(1+)*BF4(1-)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In dichloromethane-d2 at 20℃; Equilibrium constant;

...Expand

: 603-35-0
triphenylphosphine

thiocyanato: thiocyanato

: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.) Na / 1.) liquid NH3, 1 h, 2.) 2.5 h 2: 1.) Na; NH4Cl / liquid NH3, 1.) 1 h, 2.) 2.5 h View Scheme

: 113508-00-2
{tetrakis(dimethylphenylphosphine)copper(I)} bis{(trimethylsilyl)methyl}cuprate(I)

A: 75-76-3
tetramethylsilane

B: 12775-96-1, 15158-11-9, 15721-63-8, 16941-75-6, 17493-86-6, 19498-52-3, 20499-83-6, 20499-84-7, 20499-85-8, 20499-86-9, 20573-10-8, 20573-11-9, 21595-51-7, 21595-52-8, 22206-52-6, 26445-28-3, 28959-95-7, 37362-93-9, 39417-05-5, 54603-16-6, 54603-23-5, 54603-32-6, 54603-40-6, 54603-48-4, 54603-81-5, 54603-89-3, 56316-56-4, 95985-91-4, 122297-32-9, 7440-50-8
copper

C: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
With H2 In toluene Copper-complex is hydrogenated under 3 atm of H2 in toluene, the color of the soln. changes quickly from yellow to orange (under exclusion of air).; investigation by (1)H NMR;

...Expand

: cis-(molybdenum-bis(dinitrogen)(PMe2Ph)4)

: trans-(molybdenum-bis(dinitrogen)(PMe2Ph)4)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In benzene-d6 Cis-isomer is dissolved in C6D6 in a NMR-tube.; monitored by (31)P NMR for 19 days;

: trans-(molybdenum-bis(dinitrogen)(PMe2Ph)4)

: cis-(molybdenum-bis(dinitrogen)(PMe2Ph)4)

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In benzene-d6 Trans-isomer is dissolved in C6D6 in a NMR-tube.; monitored by (31)P NMR for 19 days;

: 118458-17-6
Cp2Ti(CH2CO).PMe2Ph

: 74-86-2
acetylene

A: 82808-18-2
(C5H5)2TiOCCH2CHCH

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In not given

...Expand

: 108969-89-7
Cp2TiCH2.PMe2Ph

: 554-70-1
triethylphosphine

A: 84254-01-3
Cp2TiCH2.PEt3

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In not given Kinetics; equil. react.; (31)P-NMR;

...Expand

: (dimethylphenylphosphine)bis(2,4-dimethylpentadienyl)titanium

A: bis(2,4-dimethylpentadienyl)titanium

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In tetrahydrofuran under N2, dissociation in soln.; detn. by (31)P-NMR;

: 135745-75-4, 150653-03-5
mer-trichlorotris(dimethylphenylphosphine)tungsten(III)

A: 47690-18-6
tetrachlorotris(dimethylphenylphosphine)tungsten(IV)

B: 30411-60-0
WCl4(PMe2Ph)2

C: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In not given decomposition of the mer-isomer above 90°C (Ar);

...Expand

: {Cp(PMe2Ph)2molybdenum(III) dichloride}

: 554-70-1
triethylphosphine

: {Cp(PEt3)2molybdenum(III) dichloride}

B: 672-66-2
Dimethyl(phenyl)phosphine

Conditions

Conditions	Yield
In toluene mixing of the Mo compd. with the free phosphine (molar ratio 2.0:1) in toluene;; equilibrium;

...Expand

: 75-03-6
ethyl iodide

: 672-66-2
Dimethyl(phenyl)phosphine

: 72153-49-2
dimethylethylphenylphosphonium iodide

Conditions

Conditions	Yield
In benzene at 20℃; for 12h; Inert atmosphere; Schlenk technique;	100%

: 672-66-2
Dimethyl(phenyl)phosphine

: C16H31PSi

: [(dicyclohexylphosphanyl-trimethylsilanyl-methylene)-dimethyl-λ5-phosphanyl]-benzene

Conditions

Conditions	Yield
In pentane at 0℃; Addition;	100%

: [PtW(CH(C6H4CH3))(CO)2(P(CH3)2C6H5)2(C5H5)](1+)*[BF4](1-)=[PtW(CH(C6H4CH3))(CO)2(P(CH3)2C6H5)2(C5H5)][BF4]

: 672-66-2
Dimethyl(phenyl)phosphine

: [PtW(CHC6H4CH3)(CO)2(P(CH3)2C6H5)3(C5H5)](1+)*[BF4](1-)=[PtW(CHC6H4CH3)(CO)2(P(CH3)2C6H5)3(C5H5)][BF4]

Conditions

Conditions	Yield
In dichloromethane excess of ligand in light petroleum added to stirred soln. of complex in CH2Cl2, reacted for 10 min; evapd. (vac.), washed (Et2O), dried (vac.); elem. anal.;	100%

: 12146-37-1, 124717-04-0
(bicyclo[2.2.1]hepta-2,5-diene)tetracarbonylmolybdenum(0)

: 672-66-2
Dimethyl(phenyl)phosphine

: 24554-47-0
bis(phenyldimethylphosphine)molybdenum tetracarbonyl

B: 121-46-0
bicyclo[2.2.1]hepta-2,5-diene

Conditions

Conditions	Yield
In tetrahydrofuran reaction in a calorimeter;	A 100% B n/a

...Expand

: {Pt2Cl2(PMe2Ph)4}{BF4}2

: 672-66-2
Dimethyl(phenyl)phosphine

: 56954-49-5
{PtCl(PMe2Ph)3}{BF4}

Conditions

Conditions	Yield
In acetone dissolved in acetone, PMe2Ph was added; solution was evaporated, dried in vacuo, elem. anal., NMR;	100%

: (C5H5)MoCl2(P(C6H5)3)2

: 672-66-2
Dimethyl(phenyl)phosphine

: {Cp(PMe2Ph)2molybdenum(III) dichloride}

Conditions

Conditions	Yield
In dichloromethane byproducts: P(C6H5)3; mixing of the Mo compd. with the free phosphine (molar ratio 2.8:1) in CH2Cl2;;	100%

: {Cp(PMePh2)2molybdenum(III) dichloride}

: 672-66-2
Dimethyl(phenyl)phosphine

: {Cp(PMe2Ph)2molybdenum(III) dichloride}

B: 1486-28-8
diphenyl(methyl)phosphine

Conditions

Conditions	Yield
In toluene mixing of the Mo compd. with the free phosphine (molar ratio 2.0:1) in toluene;;	A 100% B n/a

...Expand

: 33542-07-3
cis,trans-[dicarbonylbis(trimethylphosphine)(methyl)iodoiron(II)]

: 143-66-8
sodium tetraphenyl borate

: 672-66-2
Dimethyl(phenyl)phosphine

: 80700-08-9, 80736-08-9
(CO)2CH3Fe(P(CH3)3)2P(CH3)2C6H5(1+)*B(C6H5)4(1-)

Conditions

Conditions	Yield
In methanol at -30°C;	100%

...Expand

: 511550-07-5, 210559-10-7
[NEt4N][Re3(μ-H)4(CO)9(C3H4N2)]

: 672-66-2
Dimethyl(phenyl)phosphine

: 210559-25-4
[Et4N][Re3(μ-H)4(CO)9(PMe2PH)]

Conditions

Conditions	Yield
In [(2)H6]acetone N2-atmosphere; 193 to 298 K; detd. by NMR spectroscopy;	100%

: ((CH3)5C5)Ir(C2H(CH3)O2NSO2C6H4CH3)

: 672-66-2
Dimethyl(phenyl)phosphine

: ((CH3)5C5)Ir(P(CH3)2C6H5)(C2H(CH3)O2NSO2C6H4CH3)

Conditions

Conditions	Yield
In chloroform-d1 N2-atmosphere; elem. anal.;	100%

: (butane-1,4-diyl)iodo(methyl)platinum(IV)

: 672-66-2
Dimethyl(phenyl)phosphine

: 59991-54-7
(butane-1,4-diyl)bis(dimethylphenylphosphine)iodo(methyl)platinum(IV)

Conditions

Conditions	Yield
In dichloromethane room temp., stirring (30 h); filtration, volume reduction, pptn. on MeOH addn.;	100%

: C62H80Hf2N2O2(2+)*2C24BF20(1-)

: 672-66-2
Dimethyl(phenyl)phosphine

: 2C24BF20(1-)*C78H102Hf2N2O2P2(2+)

Conditions

Conditions	Yield
at 20℃; for 24h; Inert atmosphere;	100%

: sodium hexaflorophosphate

: [W(hydrotris(3,5-dimethylpyrazolyl)borate)(CO)2(η(1)-CBr)]

: 672-66-2
Dimethyl(phenyl)phosphine

: {HB(3,5-Me2C3HN2)3(CO)2WCPMe2Ph}PF6

Conditions

Conditions	Yield
In acetonitrile Inert atmosphere; Schlenk technique;	100%

...Expand

: 7333-63-3
4-bromobutylphosphonium bromide

: 672-66-2
Dimethyl(phenyl)phosphine

: 89807-18-1
C30H34P2(2+)*2Br(1-)

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 4h; Heating;	99%

: 672-66-2
Dimethyl(phenyl)phosphine

: Trifluoro-methanesulfonatetriphenyl-trifluoromethanesulfonyloxymethyl-arsonium;

: (Dimethylphenylphosphonio)(triphenylarsonio)methan-bis(trifluormethansulfonat)

Conditions

Conditions	Yield
In acetonitrile for 24h; Ambient temperature;	99%

: dinitrosylbis(triphenylphosphine)cobalt hexafluorophosphate

: 672-66-2
Dimethyl(phenyl)phosphine

: Co(NO)2(P(C6H5)(CH3)2)2(1+)*PF6(1-)=[Co(NO)2(P(C6H5)(CH3)2)2]PF6

Conditions

Conditions	Yield
In dichloromethane byproducts: PPh3; N2-atmosphere; excess of incoming phosphine, 20°C;	99%

: [(4-MePy)Fe(phthalocyanate)O]2Ru(tetrakis(4-methoxyphenyl)porphyrinate)

: 672-66-2
Dimethyl(phenyl)phosphine

: [(P(CH3)2Ph)Fe(phthalocyanate)O]2Ru(tetrakis(4-methoxyphenyl)porphyrinate)

Conditions

Conditions	Yield
In chloroform byproducts: 4-methylpyridine; excess of ligand added to Ru-Fe complex in CHCl3 at room temp.; pptn. with hexane;	99%

: 171193-96-7
[(η(5)-heptamethylindenyl)RhCl(μ-Cl)]2

: 672-66-2
Dimethyl(phenyl)phosphine

: 171193-98-9
[(η(5)-heptamethylindenyl)Rh(PMe2Ph)Cl2]

Conditions

Conditions	Yield
In tetrahydrofuran N2-atmosphere; 24 h; solvent removal (vac.), recrystn. (THF/hexane, -40°C); elem. anal.;	99%

: [Ni(C6Cl4(PPh2)-2)2]

: 672-66-2
Dimethyl(phenyl)phosphine

: [Ni(C6Cl4(PPh2)-2)2(PMe2Ph)]

Conditions

Conditions	Yield
In toluene N2-atmosphere; equimolar amts., stirring (dissoln.); sepn. on EtOH addn.; elem. anal.;	99%

: technetium tetrachloride

: 672-66-2
Dimethyl(phenyl)phosphine

: 53749-04-5
trans-[(99)TcCl4(PMe2Ph)2]

Conditions

Conditions	Yield
In benzene Schlenk technique, radiation precautions; PMe2Ph added to suspn. of TcCl4, mixt. stirred at room temp.;	99%

: 75-09-2
dichloromethane

: 7732-18-5
water

: 672-66-2
Dimethyl(phenyl)phosphine

: 7646-79-9
cobalt(II) chloride

: 7440-66-6
zinc

A: ZnCl4(2-)*2(C6H5)(CH3)3P(1+)=[(C6H5)(CH3)3P]2[ZnCl4]

B: 7440-48-4
cobalt

C: 7646-85-7
zinc(II) chloride

D: zinc(II) hydroxide

Conditions

Conditions	Yield
In dichloromethane	A n/a B 99% C n/a D n/a

...Expand

: 5717-41-9
ethyl 2-methylbuta-2,3-dienoate

: 76-05-1
trifluoroacetic acid

: 672-66-2
Dimethyl(phenyl)phosphine

: 1332456-48-0
dimethylphenyl(4-ethoxy-3-methyl-4-oxobut-1-en-2-yl)phosphonium trifluoroacetate

Conditions

Conditions	Yield
In chloroform at 20℃; for 12h;	99%

...Expand

: 3395-91-3
Methyl 3-bromopropionate

: 672-66-2
Dimethyl(phenyl)phosphine

: (3-methoxy-3-oxopropyl)dimethyl(phenyl)phosphonium bromide

Conditions

Conditions	Yield
In acetonitrile at 20℃;	99%

: 146000-78-4
methyl (E)-3-[(phenylcarbamoyl)diazenyl]but-2-enoate

: 672-66-2
Dimethyl(phenyl)phosphine

: C20H24N3O3P

Conditions

Conditions	Yield
In diethyl ether at 0 - 5℃; for 0.2h;	98%

: 79829-64-4
μ-oxo-bis[(nitrosotrimethylsilylmethane)nitrosyloxomolybdenum]

: 672-66-2
Dimethyl(phenyl)phosphine

: 79846-11-0
Mo2O3(NO)2(ONCH2Si(CH3)3)2(P(CH3)2C6H5)2

Conditions

Conditions	Yield
In toluene ppt. washed with toluene, THF and diethyl ether, dried in vac.; elem. anal.;	98%

: 182137-83-3
Re(CO)4(OC(OCH3)CHCCH2COOCH3)

: 672-66-2
Dimethyl(phenyl)phosphine

: fac-Re(CO)3(PMe2Ph)[C(CH2CO2Me)=C(H)CO2Me]

Conditions

Conditions	Yield
In hexane N2-atmosphere; refluxing (30 min); evapn. (vac.), chromy. (SiO2, hexane / CH2Cl2 = 2 : 1);	98%

: 184682-63-1
(η(5)-pentamethylcyclopentadienyl)iodo(perfluorobenzyl)carbonylcobalt(III)

: 672-66-2
Dimethyl(phenyl)phosphine

: 184682-69-7
Co(P(CH3)2C6H5)I((CH3)4C5CH2C6F4CF2)

Conditions

Conditions	Yield
In tetrahydrofuran N2-atmosphere; stirring (room temp., 19 h); evapn. (vac.);	98%

: 226922-36-7
(pentamethylcyclopentadienyl)iridium(II) hydride

: 672-66-2
Dimethyl(phenyl)phosphine

: [(Cp(*)IrH)2(μ-H)(μ-Me2PC6H4)]

Conditions

Conditions	Yield
In benzene (Ar or N2); ligand added to Ir complex in C6H6, stirred at room temp. for 16 h; evapd. (vac.), extd. (C6H6), evapd.; elem. anal.;	98%

DIMETHYLPHENYLPHOSPHINE Chemical Properties

Product Name: Dimethylphenylphosphine (CAS NO.672-66-2)

Molecular Formula: C₈H₁₁P
Molecular Weight: 138.15g/mol
Mol File: 672-66-2.mol
Einecs: 211-595-3
Appearance: Colorless to light yellow liqui
Boiling point: 193.3 °C at 760 mmHg
Storage Temperature: Flammables area
Flash Point: 50 °C
Density: 0.971 g/mL at 25 °C(lit.)
Refractive index: n20/D 1.563(lit.)
Sensitive: Air Sensitive
Enthalpy of Vaporization: 41.19 kJ/mol
Vapour Pressure: 0.653 mmHg at 25°C
XLogP3-AA: 1.5
H-Bond Donor: 0
H-Bond Acceptor: 0
Product Categories: Ligand; Catalysis and Inorganic Chemistry; Phosphine Ligands; Phosphorus Compounds

DIMETHYLPHENYLPHOSPHINE Safety Profile

Safety Information of Dimethylphenylphosphine (CAS NO.672-66-2):
Hazard Codes: Xi
Risk Statements: 10-36/37/38
10: Flammable
36: Irritating to the eyes
37: Irritating to the respiratory system
38: Irritating to the skin
Safety Statements: 26-36-16
16: Keep away from sources of ignition - No smoking
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36: Wear suitable protective clothing

DIMETHYLPHENYLPHOSPHINE Specification

Dimethylphenylphosphine ,its CAS NO. is 672-66-2,the synonyms is Phosphorus dimethyl phenyl ; Dimethylphenylphosphine ; Phenyldimethylphosphine ; Phosphine, dimethylphenyl- ; d Dimethylphenylphosphine,c69.2%,h7.9% ; Dimethylphenylphosphine,99% .

Product Name

DIMETHYLPHENYLPHOSPHINE

Synthetic route

DIMETHYLPHENYLPHOSPHINE Chemical Properties

DIMETHYLPHENYLPHOSPHINE Safety Profile

DIMETHYLPHENYLPHOSPHINE Specification

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