Conditions | Yield |
---|---|
With disulfur dichloride; iron(III) chloride In neat (no solvent) addn. of a mixt. of 140 g PCl3 and 1.7 g S2Cl2 drop by drop to a hot mixt. of 160 g PSCl3, 2 g anhydrous FeCl3 and 38 g S on stirring and refluxing (4.5 h); refluxing for 1 h, distg. off PSCl3;; | 100% |
In neat (no solvent) react. molten S with PCl3 at 124-126 °C at ambient pressure; use of a catalyst formed on melting S with active carbon and boiling in PSCl3 at 200 °C;; | |
disulfur dichloride In not given react. with S2Cl2 as catalyst;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: thiosulfate; react. on heating;; |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
phosphorus pentachloride
D
sulfur dioxide
E
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) excess of SOCl2; 180°C;; | |
In neat (no solvent) excess of SOCl2; 180°C;; |
sulfur dioxide
phosphorus trichloride
A
trichlorothiophosphine
B
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: POCl3; decompn. of SO2- and PCl3-vapours in a calcinating tube;; formation of POCl3, PSCl3 and a small amount of S;; | |
In neat (no solvent) byproducts: POCl3; decompn. of SO2- and PCl3-vapours in a calcinating tube;; formation of POCl3, PSCl3 and a small amount of S;; |
sulfur dioxide
phosphorus trichloride
A
trichlorothiophosphine
B
trichlorophosphate
Conditions | Yield |
---|---|
tetramethyl ammonium-pyrosulfite 50°C; | |
phosphorus tribromide 50°C; | |
phosphorus(V) oxybromide 50°C; |
disulfur dichloride
A
trichlorothiophosphine
B
trichlorophosphate
C
phosphorus trichloride
Conditions | Yield |
---|---|
With silica gel In neat (no solvent) byproducts: SiCl4; react. of Ca3(PO4)2 with S2Cl2 at 1000 °C in presence of SiO2;; after 1 h 9.5 % phosphate are caused to react.;; | |
In neat (no solvent) react. of Ca3(PO4)2 with S2Cl2 at 1000 °C;; after 1 h 19.5 % phosphate are caused to react.;; | |
In neat (no solvent) react. of Ca3(PO4)2 with S2Cl2 at 1000 °C;; after 1 h 19.5 % phosphate are caused to react.;; | |
With SiO2 In neat (no solvent) byproducts: SiCl4; react. of Ca3(PO4)2 with S2Cl2 at 1000 °C in presence of SiO2;; after 1 h 9.5 % phosphate are caused to react.;; |
disulfur dichloride
A
trichlorothiophosphine
B
sulfur
C
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) addn. of P (excess) to boiling S2Cl2;; |
Conditions | Yield |
---|---|
In neat (no solvent) addn. of P to boiling S2Cl2;; | |
In neat (no solvent) react. at boiling temp.;; | |
With Fe or Al In neat (no solvent) heating P with S2Cl2 in presence of Fe or Al;; | |
In neat (no solvent) heating P with S2Cl2;; |
thionyl chloride
phosphorus trichloride
A
trichlorothiophosphine
B
phosphorus pentachloride
C
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) slowly at 80-160°C;; POCl3 only supposed;; |
thionyl chloride
phosphan
A
hydrogenchloride
B
trichlorothiophosphine
D
phosphorus sulfide
E
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) room temp.;; further unidentified liquid products;; |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
sulfur dioxide
E
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D 0% E n/a |
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D 0% E n/a |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
sulfur dioxide
D
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D n/a |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
phosphorus pentachloride
D
sulfur dioxide
E
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) excess of SOCl2; 180°C;; | |
In neat (no solvent) excess of SOCl2; 180°C;; |
phosphorus trichloride
trichlorothiophosphine
Conditions | Yield |
---|---|
With sulfur at 76°C, in common pressure; | 0% |
With sulfur; barium sulfide in autoclave at 150°C for 4-5 h; | >99 |
With sulfur; calcium(II) sulfide in autoclave at 150°C for 4-5 h; | >99 |
disulfur dichloride
phosphorus trichloride
A
trichlorothiophosphine
B
phosphorus pentachloride
Conditions | Yield |
---|---|
In neat (no solvent) 6h, 160°C;; | A >99 B >99 |
In neat (no solvent) 6h, 160°C;; | A >99 B >99 |
sulfuryl dichloride
phosphorus trichloride
A
trichlorothiophosphine
B
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) simultaneous formation of POCl3 and PSCl3 via reaction of PCl3 with SO2Cl2;; isolation via fractionation;; | |
In not given react. with SO2Cl2;; fractional distn.;; | |
In not given react. with SO2Cl2;; fractional distn.;; |
disulfur dichloride
A
trichlorothiophosphine
B
trichlorophosphate
C
phosphorus trichloride
Conditions | Yield |
---|---|
With silica gel In neat (no solvent) byproducts: SiCl4; react. of Ca(PO3)2 with S2Cl2 at 1000 °C in presence of SiO2;; | |
With SiO2 In neat (no solvent) byproducts: SiCl4; react. of Ca(PO3)2 with S2Cl2 at 1000 °C in presence of SiO2;; |
disulfur dichloride
phosphorus(III) oxide
A
trichlorothiophosphine
B
sulfur dioxide
C
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: S; vigorous reaction;; |
disulfur dichloride
A
trichlorothiophosphine
B
sulfur
C
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) in coldness under inflammation;; |
phosphorus pentachloride
potassium thioacyanate
A
disulfur dichloride
B
trichlorothiophosphine
D
cyanogen chloride
Conditions | Yield |
---|---|
In neat (no solvent) haeting at lower temp.; formation of CNCl, PSCl3, KCl and a small amount of S2Cl2;; |
phosphorus pentachloride
potassium thioacyanate
A
trichlorothiophosphine
C
cyanogen chloride
Conditions | Yield |
---|---|
heating; | |
heating; |
phosphorus pentachloride
A
trichlorothiophosphine
B
thionyl chloride
D
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) heating PbS2O3 (dryed at 400 °C) with a reflux condenser; react. starting without heating, react. accelerated on heating; formation of POCl3, SOCl2, PSCl3 and PbCl2 as residue;; |
trichlorophosphate
A
trichlorothiophosphine
B
phosphoric acid
Conditions | Yield |
---|---|
In neat (no solvent) react. with P2S5 in a sealing tube at 150 °C;; | |
In neat (no solvent) heating in a sealing tube at 150 °C;; | |
In neat (no solvent) react. with P2S5 in a sealing tube at 150 °C;; |
phosphorus pentachloride
trichlorothiophosphine
Conditions | Yield |
---|---|
With metal sulfide In not given byproducts: metal chloride; react. with metal sulfides forming PSCl3 and corresponding metal chlorides;; | |
With hydrogen sulfide In neat (no solvent) byproducts: HCl; react. of dry H2S with PCl5 under heating;; | |
With hydrogen sulfide In neat (no solvent) byproducts: HCl; | |
With metal chloride In not given byproducts: metal sulfide; react. of PCl5 with metal chloride;; | |
With metal chloride In not given byproducts: metal sulfide; react. of PCl5 with metal chloride;; |
thiophosphoryl(V) bromide
phosphorus pentachloride
A
trichlorothiophosphine
B
phosphorus pentabromide
Conditions | Yield |
---|---|
In not given react. with PSBr3;; | |
In not given react. with PSBr3;; |
phosphorus pentachloride
hydrogen sulfide
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. with liquid H2S;; | |
In carbon disulfide passing H2S through a liquid mixt. of PCl5 and CS2;; distn. in a stream of CO2;; | |
In not given react. of liquid H2S with PCl5;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: thiosulfate; react. on haeting;; |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. H2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 100% B n/a |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. H2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | 100% |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile at 0 - 20℃; for 12h; | 98% |
trichlorothiophosphine
chloro bis(3,5-bis(borane-diphenylphosphino)-phenoxy)thiophosphate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; in the absence of air using Schlenk techniques; mixed between -95 and -100°C under stirring; mixt. stirred overnight at room temp.; partially concd. (vac.); ppt. centrifuged; filtered under Ar; filtrate evapd; as oil; | 97.5% |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. NO2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 97% B 3% C n/a D n/a |
trichlorothiophosphine
carbon monoxide
A
sulphur monochloride
B
PSCl2(1+)
D
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CO; the reagent ions were selected using a quadrupole massfilter before being injected into a drift region contg. helium carrier gas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 93% C 1% D 6% E n/a |
trichlorothiophosphine
dinitrogen monoxide
A
sulphur monochloride
B
PSCl2(1+)
D
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 93% C 1% D 6% E n/a |
In gas Kinetics; byproducts: O; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; O was also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 69% C 18% D 13% E n/a |
Conditions | Yield |
---|---|
In chloroform dissolving NH3-gas at -10°C in dry CHCl3; dropwisre addn. of PSCl3 in CHCl3 during 1.5 h; passing NH3 through the soln. at -10°C; sucking off; drying in vac. and dissolving in CHCl3; boiling for 3-4 h in presence of diethylamine;; recrystn. from hot methanol;; | 90% |
In chloroform dissolving NH3-gas at -10°C in dry CHCl3; dropwisre addn. of PSCl3 in CHCl3 during 1.5 h; passing NH3 through the soln. at -10°C; sucking off; drying in vac. and dissolving in CHCl3; boiling for 3-4 h in presence of diethylamine;; recrystn. from hot methanol;; | 90% |
In not given formation from PSCl3 and NH3;; |
trichlorothiophosphine
methylenebis(dichlorophosphine)
methylene-bis-(phosphonic dichloride)
Conditions | Yield |
---|---|
With aluminum (III) chloride at 110 - 140℃; for 6h; Inert atmosphere; | 89% |
trichlorothiophosphine
isopropyl alcohol
O-isopropyl phosphorodichloridothioate
Conditions | Yield |
---|---|
With pyridine at 20℃; for 2h; | 84% |
Conditions | Yield |
---|---|
Stage #1: para-tert-butylphenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 81% |
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: SCl, Cl2; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2; the reagent ions were selected using a quadrupole massfilter before being injected into a drift region contg. He; 298 K; SCl, Cl2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 80% B 4% C 2% D 14% E n/a |
trichlorothiophosphine
carbon dioxide
A
sulphur monochloride
B
PSCl2(1+)
E
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: Cl, CCl; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CO2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. He; at 298 K; Cl, CCl were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 80% C 11% D 3% E 6% |
Conditions | Yield |
---|---|
Stage #1: ortho-cresol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 80% |
Conditions | Yield |
---|---|
Stage #1: p-cresol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 76% |
Conditions | Yield |
---|---|
Stage #1: 2-fluorophenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 8h; | 75% |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. O2/N2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carrier gas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 21% B 73% C 6% D n/a |
trichlorothiophosphine
2-monochlorophenol
phosphorodichloridothioic acid O-ortho-chlorophenyl ester
Conditions | Yield |
---|---|
Stage #1: 2-monochlorophenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 8h; | 72% |
trichlorothiophosphine
carbon tetrafluoride
A
PSCl2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: CF2, CF2S, CClF2; High Pressure; ions were generated in an electron impact high-pressure ion source contg. CF4; the reagent ions were selected using a quadrupole mass filter before being injected into a region contg. He; at 298 K; CF2, CF2S, CClF2, CFS, PS were obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 4% B 2% C 69% D n/a E 25% |
trichlorothiophosphine
sulfur(VI) hexafluoride
A
ClS2(1+)
B
PSCl2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: S2(1+), PFCl3, F; High Pressure; ions generated in an electron impact high-pressure ion source contg. SF6were selected using a quadrupole mass filter before being injected into a region contg. He; 298 K; S*PSCl3(1+), SF, SFCl, S2, ClF, ClP, FS2, S2 (1+), PFCl3, F were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 4% B 14% C 69% D 6% E 3% |
trichlorothiophosphine
sulfur(VI) hexafluoride
A
FS2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: SF2, F2, PFCl3; High Pressure; the ions were generated in an electron impact high-pressure ion source contg. SF6; the ions were selected using a quadrupole mass filter before being injected into a drift region contg. He carrier gas; 298 K; SF2, F2, PFCl3, FS2, SSF2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube;; | A 8% B 66% C 13% D 8% E 5% |
Conditions | Yield |
---|---|
In water at 3 - 95℃; for 2.66667h; Product distribution / selectivity; Heating / reflux; | 65% |
trichlorothiophosphine
carbon tetrafluoride
B
SCF(1+)
C
PCl2(1+)
D
PS(1+)
E
fluorodichloromethyl(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: CFSCl3(1+), PFCl3(1+), CClS(1+); High Pressure; ions generated in an electron impact high-pressure source contg. CF4 were selected using a mass filter before being injected into a region contg. He; 298 K; CFSCl3(1+), PFCl3(1+), CClS(1+), CCl3F, PCl3, CClS, CClFS, PSCl, P, CS, PFCl2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 15% B 64% C n/a D n/a E 9% |
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: Cl, N, PS(1+); High Pressure; ions generated in an electron impact high-pressure source contg. N2 wereselected using a quadrupole mass filter before being injected into a dr ift region contg. He; at 298 K; PS(1+), Cl, N, SCl, PCl3, Cl2, NCl3 werealso obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 62% B 1% C 16% D 15% E 5% |
trichlorothiophosphine
ammonium chloride
dichlorothiophosphoric acid amide
Conditions | Yield |
---|---|
for 20h; Reflux; | 58.5% |
Conditions | Yield |
---|---|
In water for 0.5h; Product distribution / selectivity; Reflux; | 56.5% |
In water according to S.K. Yasuda, J.L. Lambert, Inorg. Synth. 1957, 5, 102; PSCl3 added to aq. NaOH; suspended in anhydr. methanol; | 42% |
In neat (no solvent) | |
In neat (no solvent) | |
In water react. of aq. NaOH and PSCl3; |
trichlorothiophosphine
A
diferrocenyl chlorothiophosphonate
Conditions | Yield |
---|---|
With NEt3 In tetrahydrofuran byproducts: NEt3HCl; Ar-atmosphere; mixing equimolar amt. of ferrocene derivative and NEt3, cooling to -78°C, slow addn. of 0.5 equiv. of PSCl3, stirring (room temp., overnight); filtration, evapn. (vac.), chromy. (SiO2, CH2Cl2); | A 49% B n/a |
trichlorothiophosphine
carbon tetrafluoride
A
PSCl2(1+)
C
Cl3FP(1+)
D
thiocarbonyl fluoride
E
chlorotrifluoromethane
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CF4; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 48% B 44% C 8% D n/a E n/a |
trichlorothiophosphine
dinitrogen monoxide
A
PSCl2(1+)
D
PCl2(1+)
E
nitrogen(II) oxide
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: ClNOS, ClNO; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a region contg. He; at 298 K; ClNO, ClNOS were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 7% B 47% C 33% D 13% E n/a |
The Thiophosphoryl chloride, with the CAS registry number 3982-91-0 and EINECS registry number 223-622-6, has the systematic name of phosphorothioic trichloride. It is a kind of is a fuming, colorless liquid with a pungent odor, and belongs to the product category of Inorganic Chemicals. It is soluble in benzene, carbon tetrachloride, chloroform, and carbon disulfide. And the molecular formula of this chemical is Cl3PS. What's more, it is used to prepare thiophosphorylate organic compounds, such as to produce insecticides.
The physical properties of Thiophosphoryl chloride are as following: (1)ACD/LogP: 0.99; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.994; (4)ACD/LogD (pH 7.4): 0.994; (5)ACD/BCF (pH 5.5): 3.355; (6)ACD/BCF (pH 7.4): 3.355 ; (7)#H bond acceptors: 0; (8)#H bond donors: 0; (9)#Freely Rotating Bonds: 0; (10)Polar Surface Area: 41.9 Å2; (11)Index of Refraction: 1.562; (12)Molar Refractivity: 30.73 cm3; (13)Molar Volume: 94.705 cm3; (14)Polarizability: 12.182×10-24cm3; (15)Surface Tension: 57.747 dyne/cm; (16)Density: 1.789 g/cm3; (17)Flash Point: °CEnthalpy of ; (18)Vaporization: 34.789 kJ/mol; (19)Boiling Point: 125 °C at 760 mmHg; (20)Vapour Pressure: 15.031 mmHg at 25°C.
Preparation of Thiophosphoryl chloride: The most common and practical synthesis of the chemcial, which is also used in industrial manufacturing, is directly reacting phosphorus trichloride with excess sulfur at 180 °C.
PCl3 + S → PSCl3
Uses of Thiophosphoryl chloride: It can hydrolyze rapidly in basic or hydroxylic solutions, such as alcohols and amines, to produce thiophosphates.
PSCl3 + 4H2O → H3PO4 + H2S + 3HCl
PSCl3 + H2O → HOP(S)Cl2 + HCl
You should be cautious while dealing with this chemical. It is harmful if swallowed, and may also cause burns. It is also harmful to aquatic organisms, and may cause long-term adverse effects in the aquatic environment. Therefore, you had better take the following instructions: Wear suitable protective clothing, gloves and eye/face protection, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice; After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer); In case of accident or if you feel unwell, seek medical advice immediately (show label where possible); Avoid release to the environment. Refer to special instructions safety data sheet.
You can still convert the following datas into molecular structure:
(1)SMILES: P(=S)(Cl)(Cl)Cl
(2)InChI: InChI=1/Cl3PS/c1-4(2,3)5
(3)InChIKey: WQYSXVGEZYESBR-UHFFFAOYAE
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
guinea pig | LC50 | inhalation | 400mg/m3 (400mg/m3) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: EXCITEMENT | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 31(12), Pg. 53, 1987. |
guinea pig | LD50 | oral | 520mg/kg (520mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 31(12), Pg. 53, 1987. | |
mouse | LC50 | inhalation | 630mg/m3 (630mg/m3) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 31(12), Pg. 53, 1987. | |
mouse | LD50 | oral | 700mg/kg (700mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 31(12), Pg. 53, 1987. | |
rat | LC50 | inhalation | 20ppm/4H (20ppm) | "Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku," Marhold, J.V., Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha, Czechoslovakia, 1972Vol. -, Pg. 17, 1972. | |
rat | LD50 | oral | 660mg/kg (660mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 31(12), Pg. 53, 1987. |
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