Sodium tetraphenylboron supplier

Name
Sodium tetraphenylboron
EINECS 205-605-5
CAS No. 143-66-8
Article Data33
CAS DataBase
Density 1.15 g/cm3
Solubility Soluble in water
Melting Point 300 °C
Formula C₂₄H₂₀BNa
Boiling Point
Molecular Weight 342.224
Flash Point
Transport Information
Appearance white powder
Safety 26-36/37
Risk Codes 22-36/37/38
Molecular Structure
Hazard Symbols Xn,Xi
Synonyms Borate(1-),tetraphenyl-, sodium (8CI,9CI);Kalibor;Kalignost;Kariporu K;Sodiumtetrakis(phenyl) borate;Sodium tetraphenylborate(NaPh4B);Sodium tetraphenylborate(1-);Sodiumtetraphenylboride(1-);Tetraphenyl boron sodium salt;Tetraphenyl sodium borate;
PSA 0.00000
LogP 3.06400

Synthetic route

: phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate anschliessendes Behandeln mit H2O und NaCl;
With sodium tetrafluoroborate; diethyl ether anschliessendes Behandeln mit wss.NaCl;

: 960-71-4
triphenylborane

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With sodium tetraethylborate In xylene Heating;

: sodium perchlorate

: 3244-41-5
potassium tetraphenylborate

A: potassium perchlorate

B: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In acetone filtration, evapn. of filtrate;
In acetone filtration, evapn. of filtrate;

...Expand

: 109-63-7
trifluoroborane diethyl ether

: 100-58-3
phenylmagnesium bromide

: 7647-14-5
sodium chloride

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
extrn. with dry acetone;
In diethyl ether; water ether layer is evapd.; residue dissolved in water; satd. with NaCl;
extrn. with dry acetone;
In diethyl ether; water ether layer is evapd.; residue dissolved in water; satd. with NaCl;

...Expand

: 13755-29-8
sodium tetrafluoroborate

: 100-58-3
phenylmagnesium bromide

: 7647-14-5
sodium chloride

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In tetrahydrofuran; water THF layer is again treated with aq. NaCl;
In tetrahydrofuran C6H5Mg is reacted with Na; poured into satd. soln. of NaCl; extrn. with THF; removing solvent in vac., stirring with CHCl3;
In not given organic layer is evapd.; residue freeing from biphenyl by extrn. with CHCl3; recrystn. from ether;

...Expand

: 7637-07-2
boron trifluoride

: 497-19-8
sodium carbonate

: 100-58-3
phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In diethyl ether; water distilling off the ether, adding H2O and calcd. amt. of Na2CO3;
In diethyl ether; water distilling off the ether, adding H2O and calcd. amt. of Na2CO3;

...Expand

: 7440-23-5
sodium

: 10294-34-5
boron trichloride

: 108-90-7
chlorobenzene

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With hydrogenchloride In xylene below 30°C; reaction mixture pured into ice, organic layer separated, washed with water, aqueous layers are neutralized with 6N HCl;

...Expand

: 124-41-4
sodium methylate

: 109-63-7
trifluoroborane diethyl ether

: 100-58-3
phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With ammonium salt

...Expand

: 109-63-7
trifluoroborane diethyl ether

: 100-58-3
phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With sodium carbonate; sodium chloride In diethyl ether water cooling, stirring, adding the BF3*(C2H5)2O soln. drop by drop, evapn. of solvent, taking up the residue with water; precipitation of Mg by adding of Na2CO3, saturation with NaCl, extrn. in Soxlet-equipment with ether;	55-60
With Na2CO3; NaCl In diethyl ether water cooling, stirring, adding the BF3*(C2H5)2O soln. drop by drop, evapn. of solvent, taking up the residue with water; precipitation of Mg by adding of Na2CO3, saturation with NaCl, extrn. in Soxlet-equipment with ether;	55-60

: 14637-34-4
ammonium tetraphenylborate

: 1310-73-2
sodium hydroxide

A: 7664-41-7
ammonia

B: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In water little excess of NaOH, boiling;
In water little excess of NaOH, boiling;

...Expand

: 13755-29-8
sodium tetrafluoroborate

: 100-58-3
phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In diethyl ether heating on water bath;
With sodium chloride In diethyl ether; water 2 h stirring, addn. of reaction mixture to a satd. aq. NaCl soln.; extrn. the aq. layer with ether two times, evapn. in vac.; recrystn. in ether at 0°C;
In diethyl ether heating on water bath;
With NaCl In diethyl ether; water 2 h stirring, addn. of reaction mixture to a satd. aq. NaCl soln.; extrn. the aq. layer with ether two times, evapn. in vac.; recrystn. in ether at 0°C;

: 14983-42-7
tris(2-methoxyethyl)borate

: 497-19-8
sodium carbonate

: 100-58-3
phenylmagnesium bromide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In water converted to the ammonium salt with NH4Cl solution (after removing the biaryls with benzene) and is then reconverted;

...Expand

: 100-59-4
phenylmagnesium chloride

: 497-19-8
sodium carbonate

: 6378-62-7
tris(2-(2-methoxyethoxy)ethyl) borate

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In water converted to the ammonium salt with NH4Cl solution (after removing the biaryls with benzene) and is then reconverted;

...Expand

: 124-41-4
sodium methylate

: 14637-34-4
ammonium tetraphenylborate

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In methanol refluxed equimolar amts. of educts under N2, solvent is subsequently evapd. and residue crystd. from ether; recrystn. from CHCl3;

: 3244-41-5
potassium tetraphenylborate

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
In acetone with cation-exchanger called Levatit S 100 or Permutit RS;
In water; acetone passing the soln. through a Na form cation exchanger;
In water; acetone passing the soln. through a Na form KU-2 resin cation exchanger;
In acetone with cation-exchanger called Levatit S 100 or Permutit RS;

: 3677-81-4
diphenylboronchloride

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With sodium In 1,2-dimethoxyethane byproducts: NaCl; Sonication; allowed to react with 2 equivs. of Na in DME with ultrasonic promotion;

: 108-86-1
bromobenzene

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
Stage #1: bromobenzene With magnesium In diethyl ether Reflux; Stage #2: With sodium tetrafluoroborate In diethyl ether for 48h;

: 13755-29-8
sodium tetrafluoroborate

phenyl halide: phenyl halide

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
Stage #1: sodium tetrafluoroborate With magnesium In tetrahydrofuran; ethylene dibromide for 0.0166667h; Sealed tube; Inert atmosphere; Schlenk technique; Stage #2: phenyl halide In tetrahydrofuran; ethylene dibromide at 20℃; for 12h; Sealed tube; Inert atmosphere; Schlenk technique;

: 13755-29-8
sodium tetrafluoroborate

: 108-86-1
bromobenzene

: 143-66-8
sodium tetraphenyl borate

Conditions

Conditions	Yield
With magnesium In tetrahydrofuran at 0 - 20℃; for 12h; Inert atmosphere;

: 127797-34-6
2,2-diiodo-5,6-dimethyl-1,3-dihydro-2-telluraindene

: 143-66-8
sodium tetraphenyl borate

: 127797-35-7
2-phenyl-2-iodo-5,6-dimethyl-1,3-dihydro-2-telluraindene

Conditions

Conditions	Yield
In ethanol for 0.25h; Heating;	100%

: 143-66-8
sodium tetraphenyl borate

: 92209-07-9
tetraisopropylphosphonium iodide

: 92209-04-6
tetraisopropylphosphonium tetraphenylborate

Conditions

Conditions	Yield
In methanol at 52℃; the structure of the product was investigated by X-ray spectroscopy;	100%

: 616-47-7
1-methyl-1H-imidazole

: 3764-01-0
2,4,6-trichloropyrimidine

: 143-66-8
sodium tetraphenyl borate

: 1,1',1''-(pyrimidin-2,4,6-triyl)-tris-3-methylimidazolium tris(tetraphenylborate)

Conditions

Conditions	Yield
In ethyl acetate Ambient temperature;	100%

...Expand

: 1122-58-3
dmap

: 3764-01-0
2,4,6-trichloropyrimidine

: 143-66-8
sodium tetraphenyl borate

: 1,1',1''-(pyrimidin-2,4,6-triyl)-tris-4-dimethylaminopyridinium tris(tetraphenylborate)

Conditions

Conditions	Yield
In ethyl acetate Ambient temperature;	100%
In ethyl acetate	100%

...Expand

: 143-66-8
sodium tetraphenyl borate

: 5-tert-Butyl-2-chloro-3,3-diphenyl-1-trimethylsilanyl-2,3-dihydro-1H-[1,2,3]azadiphosphol-3-ium; chloride

: C24H20B(1-)*C21H29ClNP2Si(1+)

Conditions

Conditions	Yield
In dichloromethane -40 deg C. then room temp., 1 h;	100%

: 585-76-2
m-bromobenzoic acid

: 143-66-8
sodium tetraphenyl borate

: 716-76-7
3-phenylbenzoic acid

Conditions

Conditions	Yield
With sodium carbonate; palladium dichloride In water at 100℃; for 4h; other reagent, temperature, reaction time;	100%
With palladium on activated charcoal; sodium carbonate for 3h; Heating;	90%
With palladium on activated charcoal; sodium carbonate at 20℃; for 24h; Product distribution; influence of catalyst, reaction time, temperature;	61%
With palladium diacetate; sodium hydroxide In water at 25℃; for 2h; Product distribution; other reagent, reaction time, temperature;	100 % Chromat.
With sodium carbonate; palladium on activated charcoal In water for 1h; Suzuki reaction; Heating;	97 % Chromat.

: 143-66-8
sodium tetraphenyl borate

: 111-64-8
n-octanoic acid chloride

: 1674-37-9
n-octanophenone

Conditions

Conditions	Yield
With palladium diacetate; sodium carbonate In acetone at 20℃; for 0.0833333h;	100%
With sodium carbonate; palladium diacetate In acetone at 20℃; for 0.0833333h; Suzuki reaction;	98%

: 143-66-8
sodium tetraphenyl borate

: 330804-78-9
1,4,7-tri(4-hexynyl)-1,4,7-triazacyclononane

: C24H39N3*C24H20B(1-)*Na(1+)

Conditions

Conditions	Yield
In methanol	100%

: 143-66-8
sodium tetraphenyl borate

[Ru(bis(N-methylimidazol-2-yl)methane))(CO)2Cl2]: [Ru(bis(N-methylimidazol-2-yl)methane))(CO)2Cl2]

: C24H20B(1-)*C9H12N4*H(1+)

Conditions

Conditions	Yield
With trifluoroacetic acid	100%

: 143-66-8
sodium tetraphenyl borate

: 501-65-5
diphenyl acetylene

: 58-72-0
Triphenylethylene

Conditions

Conditions	Yield
With water; acetic acid; bis-triphenylphosphine-palladium(II) chloride at 20℃; for 6h;	100%
With bis-triphenylphosphine-palladium(II) chloride; water; acetic acid at 20℃; for 6h; Catalytic behavior; Reagent/catalyst; Temperature; Inert atmosphere; Sealed tube;	94%

: 7681-65-4
copper(l) iodide

: 143-66-8
sodium tetraphenyl borate

: 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

Conditions

Conditions	Yield
In 1,2-dimethoxyethane Irradiation (UV/VIS); under Ar; mole ratio NaBPh4 : CuI = 1 : 1; irradn. (254 nm) for 1 h gave deposition of Cu; deposit sepd., washed with acetone and water, and dried in vac. to give pure Cu;	100%

: 143-66-8
sodium tetraphenyl borate

: 13395-16-9
copper(II) acetylacetonate

: 14024-63-6
zinc(II) acetylacetonate

A: 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

B: 7440-66-6
zinc

Conditions

Conditions	Yield
In 1,2-dimethoxyethane Irradiation (UV/VIS); under Ar; mole ratios NaBPh4 : Zn(acac)2 : Cu(acac)2 = 20 : 7 : 3; irradn. (254 nm) for 18 h gave deposition only of Cu;	A 100% B 0%

...Expand

: 143-66-8
sodium tetraphenyl borate

: zinc(II) iodide

: 7440-66-6
zinc

Conditions

Conditions	Yield
In 1,2-dimethoxyethane Irradiation (UV/VIS); under Ar; mole ratio NaBPh4 : ZnI2 = 2 : 1; irradn. (254 nm) for 2 h gave deposition of Zn; deposit sepd., washed with acetone and water, and dried in vac. to give pure Zn;	100%

: 110005-53-3
trans-acetonitrile-bis(1,2-bis(dimethylphosphino)ethane)chloroiron(II) chloride

: 143-66-8
sodium tetraphenyl borate

: 110022-38-3
trans-{iron(II)Cl(MeNC)(Me2PCH2CH2PMe2)2}{BPh4}

Conditions

Conditions	Yield
In acetonitrile 1 equiv. NaBPh4 added to a soln. of (FeCl(NCMe)(dmpe)2)Cl;; filtration; elem. anal.;;	100%

: ReO2(1+)*6C5H5N*ReO4(1-)=ReO2(C5H5N)4ReO4*2C5H5N

: 143-66-8
sodium tetraphenyl borate

: 84417-09-4
ReO2(C5H5N)4(1+)*B(C6H5)4(1-)

Conditions

Conditions	Yield
With pyridine In acetone NaBPh4 in acetone was added to a soln. of Re-compound in pyridine with 2 drops of pyridine;; H2O was added, ppt. was collected, dried, recrystd. from acetone-ether;elem. anal.;;	100%

: 15318-31-7, 14871-41-1, 59246-46-7
bis(triphenylphosphine)iridium(I) carbonyl chloride

: 143-66-8
sodium tetraphenyl borate

: 59809-88-0
[Ir(CO)3(triphenylphosphine)2]BPh4

Conditions

Conditions	Yield
With carbon monoxide In tetrahydrofuran a portion of NaBPh4 was added to a soln. of Ir-complex in THF that has been satd. with CO, mixt. was stirred for 30 min; THF was removed, residue extd. with CH2Cl2, filtered into a Schlenk flask, stirred under CO for 15 min, pentane was added to form a ppt. which can be recrystd. from CH2Cl2-pentane;	100%

: (trichlorostannyl)hexakis(tert-butyl isocyanide)molibdenum(II) hexafluorophosphate

: 143-66-8
sodium tetraphenyl borate

: Mo(CNC(CH3)3)7(2+)*2B(C6H5)4(1-)=[Mo(CNC(CH3)3)7][B(C6H5)4]2

Conditions

Conditions	Yield
In methanol stirred for 4 h, addn. of Na(BPh4);	100%

: 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

: [Ru3(C10H15)3(μ-H)3(μ3-η(3):η(3)-benzene)](BF4)2

: 143-66-8
sodium tetraphenyl borate

: [Ru3(C10H15)3(μ-H)3(μ3-η(3):η(3)-benzene)](B(C6H5)4)2*2acetone

Conditions

Conditions	Yield
In methanol room temperature;	100%

: 2637-34-5
pyridine-2-thione

: copper(ll) sulfate pentahydrate

: 143-66-8
sodium tetraphenyl borate

: Cu(1+)*2SC5H4NH*B(C6H5)4(1-)*H2O = [Cu(SC5H4NH)2]B(C6H5)4*H2O

Conditions

Conditions	Yield
In methanol; water (air); addn. of the ligand in MeOH to a soln. of the Cu salt in H2O, stirring (5 min), filtration, addn. of aq. NaBPh4, stirring (10 min); filtration, washing (H2O), drying (vac.), stirring with Et2O, filtration, repeating this extn., drying (vac.); elem.anal.;	100%

...Expand

: 166543-59-5, 257300-22-4
Pd(P(C6H5)3)2(Cl)CH2CC(C6H5)

: 166543-59-5, 257300-22-4
PdCl(P(C6H5)3)2(C(C6H5)CCH2)

: 143-66-8
sodium tetraphenyl borate

: 166939-88-4
Pd(P(C6H5)3)2(CH2CHCHC6H5)(1+)*B(C6H5)4(1-)=[Pd(P(C6H5)3)2(CH2CHCHC6H5)]B(C6H5)4

Conditions

Conditions	Yield
In chloroform-d1; [(2)H6]acetone stoich. amts.; room temp., 5 min.; (1)H NMR monitoring;	100%

...Expand

: 100228-92-0
PdCl(P(C6H5)3)2(CH2CCSi(CH3)3)

: 143-66-8
sodium tetraphenyl borate

: 166734-87-8
Pd(P(C6H5)3)2(CH2CHCHSi(CH3)3)(1+)*B(C6H5)4(1-)=[Pd(P(C6H5)3)2(CH2CHCHSi(CH3)3)]B(C6H5)4

Conditions

Conditions	Yield
In chloroform-d1; [(2)H6]acetone stoich. amts.; room temp., 5 min.; (1)H NMR monitoring;	100%

: 74-85-1
ethene

: 171511-86-7
[1,2-bis(diisopropylphosphino)ethane]chloro(pentamethylcyclopentadienyl)ruthenium(II)

: 143-66-8
sodium tetraphenyl borate

: 181778-61-0
((CH3)5C5)Ru(C2H4)((((CH3)2CH)2PCH2)2)(1+)*B(C6H5)4(1-)=[((CH3)5C5)Ru(C2H4)((((CH3)2CH)2PCH2)2)][B(C6H5)4]

Conditions

Conditions	Yield
In methanol C2H4-atmosphere; stirring (10 min); filtering, washing (EtOH, petroleum ether), drying (vac.); elem. anal.;	100%

...Expand

: tetrakis(pyridine)platinum(II) chloride trihydrate

: 143-66-8
sodium tetraphenyl borate

: [Pt(C5H5N)4](2+)*2B(C6H5)4(1-)=[Pt(C5H5N)4][B(C6H5)4]2

Conditions

Conditions	Yield
In water stirring (1 h, room temp.); washing (H2O, iPrOH, Et2O), drying (vac.);	100%

: tris([tri(tert-butyl)phosphine]gold(I))oxonium tetrafluoroborate

: 143-66-8
sodium tetraphenyl borate

: 172532-09-1
phenyl[tri(tert-butyl)phosphine]gold(I)

Conditions

Conditions	Yield
In ethanol byproducts: NaBF4, PhBO; N2-atmosphere; excess NaBPh4, stirring at room temp. in absence of direct light for 15 d (crystn.);	100%

: 37366-09-9
dichloro(benzene)ruthenium(II) dimer

: cyclopentadienylthallium(I)

: 143-66-8
sodium tetraphenyl borate

: 72804-54-7
(η(6)-benzene)(η(5)-2,4-cyclopentadien-1-yl)ruthenium tetraphenylborate

Conditions

Conditions	Yield
In water; acetonitrile N2-atmosphere; stirring Ru-complex with excess TlCp (in dark, in MeCN, 5h), filtration, addn. of H2O, filtration, addn. of excess NaBPh4 (in H2 O), stirring for 30 min; pptn. on concn., filtration, washing (H2O), drying (vac.); can be recrystallized (MeCN/Et2O); elem. anal.;	100%

...Expand

: dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer

: P,P,P'-tris[(+)-9-phenyldeltacyclan-8-yl]-1,2-bis(phosphanyl)benzene

: 143-66-8
sodium tetraphenyl borate

: [Cp*Rh(P,P,P'-tris[(+)-9-phenyldeltacyclan-8-yl]-1,2-bis(phosphanyl)benzene)Cl]BPh4

Conditions

Conditions	Yield
In methanol under N2 atm. soln. ligand and ((Cp*RhCl)2(μ-Cl))2 in MeOH was stirred at room temp. for 30 min, NaBPh4 was added and stirred for 2 h; solvent was removed in vacuo, residue was dissolved in CH2Cl2 and filtered through Celite, solvent was removed; elem. anal.;	100%

...Expand

: 66320-81-8
(η(5)-C5H5)2Ti(η(2)-CO(i-Pr))I

: 143-66-8
sodium tetraphenyl borate

: 670-54-2
ethenetetracarbonitrile

: 179097-41-7
(η(5)-C5H5)2Ti(η(2)-CO(i-Pr))(NCBPh3)

Conditions

Conditions	Yield
In methanol Ar-atmosphere; mixing equimolar amts. of Ti-complex and TCNE, addn. of 2equiv. NaBPh4;	100%

...Expand

: 143-66-8
sodium tetraphenyl borate

: 536755-29-0
N,N'-dimethylimidazolium-2-carboxylate

: 478081-95-7
1,3-dimethylimidazolium tetraphenylborate

Conditions

Conditions	Yield
With water In tetrahydrofuran Inert atmosphere;	100%

: 143-66-8
sodium tetraphenyl borate

: 1,3-bis(2,6-diisopropylphenyl)imidazolinium-2-carboxylate

: 1,3-bis(2,6-diisopropylphenyl)-imidazolium tetraphenylborate

Conditions

Conditions	Yield
With water In tetrahydrofuran Inert atmosphere;	100%

Sodium tetraphenylboron Chemical Properties

Empirical Formula: C₂₄H₂₀BNa
Molecular Weight: 342.2164
EINECS: 205-605-5
Melting point: 300 °C
Storage tempreture: 2-8 °C
Solubility: Soluble in water
Sensitive: Light sensitive
Appearance: White powder
Structure of Sodium tetraphenylboron (CAS NO.143-66-8):

IUPAC Name: Sodium tetraphenylboranuide
Canonical SMILES: [B-](C1=CC=CC=C1)(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Na+]
InChI: InChI=1S/C24H20B.Na/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;/q-1;+1
InChIKey: HFSRCEJMTLMDLI-UHFFFAOYSA-N
Product Category of Sodium tetraphenylboron (CAS NO.143-66-8): Boron compounds;Organometallics;Na (Sodium) Compounds (excluding simple sodium salts);Analytical Chemistry;Ion Association;Tetraphenylborates;Typical Metal Compounds

Sodium tetraphenylboron Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
rat	LD50	oral	288mg/kg (288mg/kg)	BEHAVIORAL: MUSCLE WEAKNESS	National Technical Information Service. Vol. OTS0555250,

Sodium tetraphenylboron (CAS NO.143-66-8) hasn't been listed as a carcinogen by NTP, IARC, ACGIH, or CA Prop 65. And the toxicological properties have not been fully investigated. You can see actual entry in RTECS for complete information.

Sodium tetraphenylboron Safety Profile

Hazard Codes: Harmful Xn, Irritant Xi
Risk Statements: 22-36/37/38
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36/37-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37:Wear suitable protective clothing and gloves.
S36:Wear suitable protective clothing.

Sodium tetraphenylboron Specification

(R)-2-Amino-3-methoxypropanoic acid hydrochloride , its cas register number is Sodium tetraphenylborate ; Tetraphenylboron sodium ; and Tetraphenyl boron sodium salt . It is hazardous, so the first aid measures and others should be known. Such as: When on the skin: first, should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly, get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While, it's inhaled: Remove from exposure and move to fresh air immediately. Give artificial respiration while not breathing. When breathing is difficult, give oxygen. And as soon as to get medical aid. Then you have the ingesting of the product: Wash mouth out with water, and get medical aid immediately. Notes to physician: Treat supportively and symptomatically.
In addition, Sodium tetraphenylboron (CAS NO.143-66-8) is light sensitive. It is not compatible with strong oxidizing agents, and you must not take it with incompatible materials, light, excess heat. And also prevent it to broken down into hazardous decomposition products: Carbon monoxide, carbon dioxide, metallic oxides, boron oxides.

Product Name

Sodium tetraphenylboron

Synthetic route

Sodium tetraphenylboron Chemical Properties

Sodium tetraphenylboron Toxicity Data With Reference

Sodium tetraphenylboron Safety Profile

Sodium tetraphenylboron Specification

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