Conditions | Yield |
---|---|
With trichlorophosphate at 10℃; for 2h; Autoclave; Reflux; | 99.2% |
With titanium tetrachloride; trichlorophosphate at 50 - 65℃; for 9h; | 94% |
With trichlorophosphate at 100℃; |
Conditions | Yield |
---|---|
With trichlorophosphate 1.) 25-30 deg C, 3 h, 2.) 50-60 deg C, 6 h; | 91% |
With trichlorophosphate at 25 - 40℃; | |
With tetrachloromethane; trichlorophosphate bei Siedetemperatur; |
Conditions | Yield |
---|---|
With potassium permanganate | |
With chlorine; 2-chloro-ethanol | |
With phosphoric acid In nitromethane |
Conditions | Yield |
---|---|
With phosphoric acid; chlorine |
2-chloro-ethanol
trichlorophosphate
Tris(2-chloroethyl) phosphate
Tris(2-chloroethyl) phosphate
Conditions | Yield |
---|---|
at 80℃; for 20h; | 100% |
chloral hydrate
Tris(2-chloroethyl) phosphate
(2,2,2-trichloro-1-hydroxy-ethyl)-phosphonic acid bis-(2-chloro-ethyl) ester
Conditions | Yield |
---|---|
In hexane Heating; | 82% |
Conditions | Yield |
---|---|
With 2,6-di-tert-butyl-4-methyl-phenol; N-benzyl-N,N,N-triethylammonium chloride In N,N-dimethyl-formamide 1.) 110 deg C, 2 h, 2.) 130 deg C, 1 h; | 46% |
Tris(2-chloroethyl) phosphate
1-cyclohexylcyclohexane-1-carboxylic acid
Conditions | Yield |
---|---|
With sodium carbonate |
Conditions | Yield |
---|---|
With barium dihydroxide |
Tris(2-chloroethyl) phosphate
Conditions | Yield |
---|---|
With silver(l) oxide nachfolgendes Umsetzen mit Barytwasser; | |
With water; lead(II) oxide nachfolgendes Umsetzen mit Barytwasser; |
Conditions | Yield |
---|---|
erfolgt Zersetzung; |
Tris(2-chloroethyl) phosphate
trimethylamine
phosphoric acid tris-(2-trimethylammonio-ethyl ester); tris chloride
Conditions | Yield |
---|---|
With ethanol at 30 - 33℃; | |
With benzene at 80℃; |
Tris(2-chloroethyl) phosphate
1-Nitropropen
isopropenyl-phosphonic acid bis-(2-chloro-ethyl ester)
Tris(2-chloroethyl) phosphate
phenylphosphonous acid dichloride; compound with aluminium trichloride (1:1)
A
Dichlorophenylphosphine
Conditions | Yield |
---|---|
With phosphorus trichloride at 30℃; for 0.333333h; Product distribution; complexes of various arylphosphonous dichlorides with aluminum chloride; |
Tris(2-chloroethyl) phosphate
water
phosphoric acid bis-(2-hydroxy-ethyl) ester
Tris(2-chloroethyl) phosphate
phosphoric acid bis-(2-hydroxy-ethyl) ester
Tris(2-chloroethyl) phosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 46 percent / Et3BnNCl, ionol / dimethylformamide / 1.) 110 deg C, 2 h, 2.) 130 deg C, 1 h 2: 91 percent / dioxane / 3 h / 50 - 60 °C View Scheme |
Tris(2-chloroethyl) phosphate
nickel diacetate
Conditions | Yield |
---|---|
In neat (no solvent) refluxing nickel(II) acetate and tris(2-chloroethyl)phosphate at 170 - 180°C in vacuo; adding ether, filtering ppt., drying in vacuo; elem. anal.; |
Tris(2-chloroethyl) phosphate
cobalt(II) acetate
Conditions | Yield |
---|---|
In neat (no solvent) refluxing cobalt(II) acetate and tris(2-chloroethyl)phosphate at 170 - 180°C in vacuo; adding ether, filtering ppt., drying in vacuo; elem. anal.; |
Conditions | Yield |
---|---|
In neat (no solvent) refluxing cobalt(II) chloride and tris(2-chloroethyl)phosphate at 170 - 180°C in vacuo; adding ether, filtering ppt., drying in vacuo; elem. anal.; |
Conditions | Yield |
---|---|
In neat (no solvent) refluxing nickel(II) chloride and tris(2-chloroethyl)phosphate at 170 - 180°C in vacuo; adding ether, filtering ppt., drying in vacuo; elem. anal.; |
Tris(2-chloroethyl) phosphate
chromium(III) chloride
(tris(2-chloroethoxy)phosphato)chromium(III)
Conditions | Yield |
---|---|
In neat (no solvent) refluxing in vac.; elem. anal.; |
Tris(2-chloroethyl) phosphate
vanadium(III) chloride
(tris(2-chloroethoxy)phosphato)vanadium(III)
Conditions | Yield |
---|---|
In neat (no solvent) refluxing in vac.; elem. anal.; |
Tris(2-chloroethyl) phosphate
(bis(2-chloroethoxy)phosphato)oxovanadium(IV)
Conditions | Yield |
---|---|
In neat (no solvent) refluxing at 160-180°C; elem. anal.; |
IARC Cancer Review: Group 3 IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 48 , 1990,p. 109.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Inadequate Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 48 , 1990,p. 109.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) . Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.
Tris(2-chloroethyl) phosphate, its cas register number is 115-96-8. It also can be called Phosphoric acid tris(2-chloroethyl)ester; TCEP; Amgard TCEP; Celluflex; Disflamoll TCA; Ethanol, 2-chloro-, phosphate (3:1); Niax Flame Retardant 3CF; Tris(2-chloroethyl) orthophosphate. It is a odorless clear liquid and slightly water soluble.It is incompatible with strong oxidizing agents and strong bases.
Physical properties about this chemical are: (1)ACD/LogP: 1.468; (2)ACD/LogD (pH 5.5): 1.47; (3)ACD/LogD (pH 7.4): 1.47; (4)ACD/BCF (pH 5.5): 7.69; (5)ACD/BCF (pH 7.4): 7.69; (6)ACD/KOC (pH 5.5): 149.89; (7)ACD/KOC (pH 7.4): 149.89; (8)#H bond acceptors: 4; (9)#Freely Rotating Bonds: 9; (10)Index of Refraction: 1.463; (11)Molar Refractivity: 56.503 cm3; (12)Molar Volume: 204.964 cm3; (13)Polarizability: 22.4 10-24cm3; (14)Surface Tension: 40.5740013122559 dyne/cm; (15)Density: 1.393 g/cm3; (16)Flash Point: 232.222 °C; (17)Enthalpy of Vaporization: 56.826 kJ/mol; (18)Boiling Point: 347.374 °C at 760 mmHg
Uses of Tris(2-chloroethyl) phosphate: Tris(2-chloroethyl) phosphate (TCEP) is a chemical compound used as a flame retardant, plasticizer, and viscosity regulator in various types of polymers including polyurethanes, polyester resins, and polyacrylates.
When you are using this chemical, please be cautious about it as the following:
1. Wear suitable protective clothing and gloves;
2. Avoid release to the environment. Refer to special instructions safety data sheet;
You can still convert the following datas into molecular structure:
(1)InChI=1S/C6H12Cl3O4P/c7-1-4-11-14(10,12-5-2-8)13-6-3-9/h1-6H2;
(2)InChIKey=HQUQLFOMPYWACS-UHFFFAOYSA-N;
(3)SmilesP(=O)(OCCCl)(OCCCl)OCCCl;
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | oral | 1866mg/kg (1866mg/kg) | National Technical Information Service. Vol. AD-A067-313, | |
mouse | LDLo | intraperitoneal | 250mg/kg (250mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) | "Summary Tables of Biological Tests," National Research Council Chemical-Biological Coordination Center. Vol. 7, Pg. 396, 1955. |
rabbit | LDLo | skin | 2gm/kg (2000mg/kg) | GASTROINTESTINAL: OTHER CHANGES SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | National Technical Information Service. Vol. OTS0517716, |
rat | LD50 | oral | 1230mg/kg (1230mg/kg) | Bulletin of Environmental Contamination and Toxicology. Vol. 17, Pg. 720, 1977. |
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