As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for the fine c
Cas:688-73-3
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Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting Tributyltin Hydride; TBTH;Tributylstannane; CAS:688-73-3 , Please contact us by email freely. We are leading exporter in China.
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Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:688-73-3
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediat
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inquiryProduct name: Tri-N-Butyltin Hydride CAS No.:688-73-3 Molecule Formula:C12H27Sn Molecule Weight:290.05 Purity: 98.0% Package: 50kg/drum Description:Light yellow near colorless liquid Manufacture Standards:Enterprise Standard
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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Conditions | Yield |
---|---|
In pentane -78°C; 3 h; | 100% |
In not given | 99.8% |
In not given | 99.8% |
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane formation at room temperature;; | 96% |
In 1,2-dimethoxyethane formation at room temperature;; | 96% |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: LiCl, Ti(Sn(C4H9)3)1.7; addn. of Bu3SnLi to Ti-compound in soln. (-78°C), stirred, mixt. brought to 20°C, soln. became blue; evapn. in vac., residue washed with pentane, sublimation (10**-3 Torr, 90°C); elem. anal., chromy.; | A 90% B 0% C 30% D 96% |
Conditions | Yield |
---|---|
95% | |
With aluminium amalgame In not given formation on reaction for 6 h at 10°C;; | 60% |
With aluminium amalgame In not given formation on reaction for 6 h at 10°C;; | 60% |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: 1-naphthylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 3 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 95% |
In tetrahydrofuran byproducts: 1-naphthylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 72% |
Conditions | Yield |
---|---|
With (SiH(CH3)O)(n) exothermic react.; | 95% |
Conditions | Yield |
---|---|
In pentane formation at -78°C;; | 94.4% |
In pentane formation at -78°C;; | 94.4% |
chloro(methyl)phenylsilane
tributyltin ethoxide
A
diethoxy-methyl-phenyl-silane
B
tributyltin chloride
C
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
2:1; room temp.; | A 94% B n/a C n/a |
2:1; room temp.; | A 94% B n/a C n/a |
tributyltin methoxide
(+)-methyl-(α-naphthyl)-phenylsilane
A
methoxy(methyl)(1-naphthyl)phenylsilane
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In toluene Kinetics; 100°C; 12 h;; | A 92% B n/a |
In toluene Kinetics; 100°C; 12 h;; | A 92% B n/a |
tributyltin ethoxide
(+)-methyl-(α-naphthyl)-phenylsilane
A
CH3(C6H5)(1-C10H7)SiOC2H5
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
100°C; 12 h; | A 92% B n/a |
100°C; 12 h; | A 92% B n/a |
100°C; 12 h; | A 92% B n/a |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: p-anisylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 91% |
dimethylamine borane
tributylstannyl trifluoromethanesulfonate
A
(μ-dimethylamino)diborane
B
tri-n-butyl-tin hydride
C
cyclic(dimethylamino borane) dimer
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethylpiperidine In further solvent(s) byproducts: H2; N2 or Ar; 1,2-dichlorobenzene soln. of nBuSnOTf (0.39 mmol) and 2,2,6,6-tetramethylpiperidine (0.4 mmol) added to soln. of B compd. (0.42 mmol), mixt. stirred at 20°c for 2 h; NMR; | A 2% B n/a C 91% |
sodium tetrahydroborate
bis(tri-n-butyltin)oxide
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In ethanol Sn compd. dissolved in abs. ethanol at 0°C under Ar, then added NaBH4, allowed to warm to room temp., stirred for 1 h; EtOH removed in vac., residue dissolved in hexane, washed with water, dried, evapd. under reduced pressure; | 90% |
tributyltin methoxide
(S)-(-)-α-naphthylphenylmethylsilane
A
methoxy(methyl)(1-naphthyl)phenylsilane
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In toluene Kinetics; 100°C; 12 h;; | A 90% B n/a |
In toluene Kinetics; 100°C; 12 h;; | A 90% B n/a |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: o-anisylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 90% |
tributyltin ethoxide
(S)-(-)-α-naphthylphenylmethylsilane
A
CH3(C6H5)(1-C10H7)SiOC2H5
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
100°C; 12 h; | A 89% B n/a |
100°C; 12 h; | A 89% B n/a |
100°C; 12 h; | A 89% B n/a |
Conditions | Yield |
---|---|
With poly(methylhydrosiloxane) In not given to Bu3SnOMe poly(methylhydrosiloxane) was added and stirred at room temp. for 8 h; distillation under reduced pressure; | 89% |
Multi-step reaction with 2 steps 2: C6H5(CH3)2SiH View Scheme | |
Multi-step reaction with 2 steps 2: C6H5(CH3)2SiH View Scheme |
Tri-n-butyl-tri-n-butyl-siloxy-zinn
poly(methylhydrosiloxane)
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In not given formation at room temperature;; distillation;; | 88% |
In not given formation at room temperature;; distillation;; | 88% |
Tri-n-butyl-tri-n-butyl-siloxy-zinn
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
1:2; 150°C; | 88% |
1:2; 150°C; | 88% |
lithium aluminium tetrahydride
tributyltin chloride
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In diethyl ether heating on reflux for 2-4 h; decomposition of excess LiAlH4 on addn. of ice-water;; distillation;; | 87% |
In diethyl ether heating on reflux for 2-4 h; decomposition of excess LiAlH4 on addn. of ice-water;; distillation;; | 87% |
In diethyl ether heating on reflux for 2-4 h; decomposition of excess LiAlH4 on addn. of ice-water;; distillation;; | 74% |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: o-tolylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 86% |
Conditions | Yield |
---|---|
In not given formation at room temperature;; distillation;; | 86% |
In not given formation at room temperature;; distillation;; | 86% |
Methyl-phenyl-ethoxy-silan
tributyltin ethoxide
A
diethoxy-methyl-phenyl-silane
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
1:1; room temp.; | A 86% B n/a |
1:1; room temp.; | A 86% B n/a |
Conditions | Yield |
---|---|
1:1; 30 min; little contaminated with siloxane fragments; | 86% |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: phenylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 85% |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: p-tolylboronic acid; to srirred soln. of Sn-compound in THF was added soln. of BH3 in THF under N2, mixt. was left at room temp. for 1 h, refluxed for 1 h, cooled, Et2O and water was added; dried with MgSO4, solvent was removed under vac., column chromy. on silica gel with hexane and hexane-Et2O, recrystd. from water; | 84% |
poly(methylhydrosiloxane)
bis(tri-n-butyltin)oxide
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In not given formation at room temperature;; distillation;; | 79% |
In not given formation at room temperature;; distillation;; | 79% |
Cyclohexyloxy-tributyl-stannan
(+)-methyl-(α-naphthyl)-phenylsilane
B
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
for 88 h at 120°C; retention >87%; | A 79% B n/a |
for 88 h at 120°C; retention >87%; | A 79% B n/a |
for 88 h at 120°C; retention >87%; | A 79% B n/a |
tributyltin formate
A
tri-n-butyl-tin hydride
B
bis(tri-n-butyltin)
C
tetra-n-butyltin(IV)
Conditions | Yield |
---|---|
heating 11.5 h at 150 to 185°C; | A 6.9% B 77.5% C 5.2% |
heating 11.5 h at 150 to 185°C; | A 6.9% B 77.5% C 5.2% |
In neat (no solvent) byproducts: CO2; heating for 11.5 h at 150-185°C under N2;; | A 6.9% B n/a C n/a |
tributyl(tris(phenyl)siloxy)tin
poly(methylhydrosiloxane)
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
In not given formation at room temperature;; distillation;; | 76% |
In not given formation at room temperature;; distillation;; | 76% |
tri-n-butyl-tin hydride
Methyl 2-butynoate
methyl (2E)-3-(tributylstannyl)but-2-enoate
Conditions | Yield |
---|---|
Stage #1: tri-n-butyl-tin hydride With n-butyllithium In tetrahydrofuran at -78℃; for 0.166667h; Stage #2: With methanol In tetrahydrofuran at -78℃; for 0.05h; Stage #3: Methyl 2-butynoate In tetrahydrofuran at -78℃; for 1.5h; | 100% |
tri-n-butyl-tin hydride
cyclohexa-1,3-diene
tributyl(cyclohex-2-en-1-yl)stannane
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In benzene at 20℃; for 1h; Inert atmosphere; | 100% |
With tetrakis(triphenylphosphine) palladium(0) In benzene at 20℃; for 0.166667h; Inert atmosphere; | 78% |
tetrakis(triphenylphosphine) palladium(0) In benzene at 20℃; for 0.25h; | 78.6% |
tri-n-butyl-tin hydride
acetylenedicarboxylic acid diethyl ester
(CH3CH2CH2CH2)3SnC(COOC2H5)CHCOOC2H5
Conditions | Yield |
---|---|
0°C;; cis-trans-ratio = 10:1;; | 100% |
0°C;; cis-trans-ratio = 10:1;; | 100% |
In not given |
Conditions | Yield |
---|---|
With diisobutylaluminium hydride 75-80°C;; | 100% |
With (iso-C4H9)2AlH 75-80°C;; | 100% |
With diisobutylaluminium hydride 75-80°C;; | 100% |
tri-n-butyl-tin hydride
phenylacetylene
(E)-1-phenyl-(2-tributylstannyl)ethene
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); oxygen In benzene-d6 at 80℃; for 2h; diastereoselective reaction; | 100% |
In not given 100-150°C, 48 h; | 93% |
With C44H72O4Ru2(2-) In tetrahydrofuran at 30℃; for 0.166667h; Solvent; UV-irradiation; Inert atmosphere; stereoselective reaction; | 92% |
perfluorobenzaldehyde
tri-n-butyl-tin hydride
A
Perfluorphenylmethoxytributylzinn
B
Perfluorphenylmethyl-(perfluorphenyl-tributylstannoxymethyl)-ether
Conditions | Yield |
---|---|
In neat (no solvent) 2:3 mole ratio of (C4H9)3SnH and aldehyde, 20. degree.C; 2.6:1 mixt. of (C4H9)3SnOCH2C6F5 and the 1:2 adduct (C4H9)3SnOCH(C6F5)OCH2C5F6; | A 100% B n/a |
In neat (no solvent) 2:3 mole ratio of (C4H9)3SnH and aldehyde, 20. degree.C; 2.6:1 mixt. of (C4H9)3SnOCH2C6F5 and the 1:2 adduct (C4H9)3SnOCH(C6F5)OCH2C5F6; | A 100% B n/a |
In not given reaction at 20°C;; |
chloro-trimethyl-silane
tri-n-butyl-tin hydride
trimethylsilyltributyltin
Conditions | Yield |
---|---|
In tetrahydrofuran 1) DIPA, THF, -78°C; 2)TMSCl, room temp.; | 100% |
With n-butyllithium; diisopropylamine In tetrahydrofuran cooling of soln. of diisopropylamine in THF to -78°C for 10 min; addn. of n-BuLi for 5 min; after 5 min heating to room temp.; addn. of SnH(n-Bu)3 for 5 min; stirring at room temp. for 20 min; addn. of Me3SiCl; stirring at room temp. for >10 min; evapn., chromy. on silica gel (hexanes); | 99% |
In neat (no solvent) deprotonation of (C4H9)3HSn with LDA followed by quench with (CH3)3SiCl; |
tri-n-butyl-tin hydride
benzenesulphonyl isocyanate
N-<(Tri-n-butylstannyloxy)-methylen>-benzolsulfonamid
Conditions | Yield |
---|---|
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
Conditions | Yield |
---|---|
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
CH2CHC(CH3)(SO2C6H4CH3)CH2CH2COOCH3
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In benzene under N2 a mixture of Sn-compound, sulfone, and AIBN in dry benzene wasrefluxed for 5 h; evapd.; | 100% |
4-methoxybenzenesulfonyl isocyanate
tri-n-butyl-tin hydride
(C4H9)3SnOCHNSO2C6H4OCH3
Conditions | Yield |
---|---|
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
tri-n-butyl-tin hydride
4-Chlorophenylsulfonyl isocyanate
(C4H9)3SnOCHNSO2C6H4Cl
Conditions | Yield |
---|---|
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
In cyclohexane 1:1 mole ratio of educts, at room temp.; | 100% |
tri-n-butyl-tin hydride
(+)-(1S,3S,4R)-menthyl pyruvate
Conditions | Yield |
---|---|
Irradiation (UV/VIS); accelerated by UV light; two diastereomeric isomers in equal amts.; | 100% |
Irradiation (UV/VIS); accelerated by UV light; two diastereomeric isomers in equal amts.; | 100% |
tri-n-butyl-tin hydride
(but-2-yn-1-yloxy)(tert-butyl)dimethylsilane
C22H48OSiSn
Conditions | Yield |
---|---|
In tetrahydrofuran; benzene-d6 at 50℃; for 18h; | 100% |
5-O-benzyl-1,3-O-methyl-2-O-[(methylthio)thiocarbonyl]-α-D-ribo-furanose
tri-n-butyl-tin hydride
5-O-benzyl-1,3-O-dimethyl-2-O-tributylstannylmethylthio-α-D-ribo-furanose
Conditions | Yield |
---|---|
Stage #1: 5-O-benzyl-1,3-O-methyl-2-O-[(methylthio)thiocarbonyl]-α-D-ribo-furanose With triethyl borane In benzene at 20℃; for 0.0833333h; Stage #2: tri-n-butyl-tin hydride In benzene for 1.3h; | 100% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); oxygen In benzene-d6 at 80℃; for 2h; diastereoselective reaction; | 100% |
With C44H72O4Ru2(2-) at 30℃; for 0.166667h; Reagent/catalyst; Time; UV-irradiation; stereoselective reaction; | 99 %Spectr. |
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
With triethyl borane In tetrahydrofuran; hexane at 80℃; for 4h; | 100% |
With triethyl borane In tetrahydrofuran; hexane at 80℃; for 4h; Temperature; | 100% |
(tert-butyldimethylsilyl)acetylene
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
Stage #1: (tert-butyldimethylsilyl)acetylene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: tri-n-butyl-tin hydride In tetrahydrofuran; hexane at -78℃; for 3h; | 100% |
2,2-dimethyl-3-butyne
tri-n-butyl-tin hydride
tributyl(3,3-dimethyl-1-butyn-1-yl)stannane
Conditions | Yield |
---|---|
Stage #1: 3,3-Dimethylbut-1-yne With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Stage #2: tri-n-butyl-tin hydride In tetrahydrofuran; hexane at -78℃; for 1h; | 100% |
With pyridine; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; zinc trifluoromethanesulfonate at 70℃; for 8h; Schlenk technique; Inert atmosphere; chemoselective reaction; | 57% |
2-methyl-6-phenylhex-3-yn-2-ol
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
With [RuCl2pentamethylcyclopentadiene]n In dichloromethane for 0.0833333h; Inert atmosphere; | 100% |
With [RuCl2pentamethylcyclopentadiene]n In dichloromethane for 1.08333h; Schlenk technique; Inert atmosphere; | 5.16 g |
tri-n-butyl-tin hydride
(4R,5R,E)-5-hydroxy-4,6-dimethyl-N-(prop-2-yn- 1-yl)hept-2-enamide
Conditions | Yield |
---|---|
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(l) cyanide In tetrahydrofuran; hexane at -78℃; for 0.583333h; Inert atmosphere; Sealed tube; Stage #2: (4R,5R,E)-5-hydroxy-4,6-dimethyl-N-(prop-2-yn- 1-yl)hept-2-enamide In tetrahydrofuran; hexane at -78℃; for 1.25h; Inert atmosphere; Sealed tube; | 100% |
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(I) cyanide In tetrahydrofuran; hexane at -78℃; for 0.5h; Inert atmosphere; Stage #2: (4R,5R,E)-5-hydroxy-4,6-dimethyl-N-(prop-2-yn- 1-yl)hept-2-enamide In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; | 100% |
With n-butyllithium; copper(l) cyanide | 100% |
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(l) cyanide In tetrahydrofuran; hexane for 0.583333h; Inert atmosphere; Stage #2: (4R,5R,E)-5-hydroxy-4,6-dimethyl-N-(prop-2-yn- 1-yl)hept-2-enamide In tetrahydrofuran; hexane for 1.25h; Inert atmosphere; | 100% |
tri-n-butyl-tin hydride
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); N-ethyl-N,N-diisopropylamine; tricyclohexylphosphine tetrafluoroborate In dichloromethane at 0℃; for 2.5h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With n-butyllithium; copper(I) cyanide | 100% |
Conditions | Yield |
---|---|
With n-butyllithium; copper(I) cyanide | 100% |
Conditions | Yield |
---|---|
at 20℃; for 24h; Temperature; Inert atmosphere; Schlenk technique; Glovebox; | 100% |
Conditions | Yield |
---|---|
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(l) cyanide In tetrahydrofuran; hexane for 0.583333h; Inert atmosphere; Stage #2: C20H27NO4 In tetrahydrofuran; hexane for 1.25h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(l) cyanide In tetrahydrofuran; hexane for 0.583333h; Inert atmosphere; Stage #2: C13H21NO2 In tetrahydrofuran; hexane for 1.25h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: tri-n-butyl-tin hydride With n-butyllithium; copper(l) cyanide In tetrahydrofuran; hexane for 0.583333h; Inert atmosphere; Stage #2: C13H21NO2 In tetrahydrofuran; hexane for 1.25h; Inert atmosphere; | 100% |
-butyl vinyl ether
tri-n-butyl-tin hydride
<2-Butyloxy-ethyl>-triisobutyl-zinn
Conditions | Yield |
---|---|
In neat (no solvent) other Radiation; under Ar; (60)Co-irradiation; 1.5:1 molar ratio (olefine:Sn-compound) ;25°C; GLC; | 99% |
other Radiation; gamma-radiation;; | 99% |
other Radiation; gamma-radiation;; | 99% |
In not given other Radiation; γ-radiation;; |
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