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| CAS No.: | 32315-10-9 |
|---|---|
| Name: | Triphosgene |
| Article Data: | 15 |
| Cas Database | |
| Molecular Structure: | |
|
|
|
| Formula: | C3Cl6O3 |
| Molecular Weight: | 296.749 |
| Synonyms: | Carbonicacid, bis(trichloromethyl) ester (6CI,8CI);Methanol, trichloro-, carbonate(2:1) (9CI);Bis(trichloromethyl) carbonate;Bis(trichloromethyl)carbonate; |
| EINECS: | 250-986-3 |
| Density: | 1.898 g/cm3 |
| Melting Point: | 78-82 °C |
| Boiling Point: | 204.5 °C at 760 mmHg |
| Flash Point: | 53.3 °C |
| Solubility: | practically insoluble in water |
| Appearance: | White solid |
| Hazard Symbols: |
 T+,  Xn
|
| Risk Codes: | 26-34-29-36/37/38-20/21/22 |
| Safety: | 36/37/39-45-9-26-36-7/9 |
| Transport Information: | UN 2928 6.1/PG 2 |
| PSA: | 35.53000 |
| LogP: | 3.79500 |
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- 3232-62-0Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylicacid, 1,4,5,6,7,7-hexachloro-, 2,3-di-2-propen-1-yl ester
- 32326-25-33-Isoxazolamine,5-methoxy-
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- 32327-52-9Borane,tris(1,2-dimethylpropyl)-
- 32327-71-2Benzenepropanenitrile,4-chloro-
- 616-38-6
carbonic acid dimethyl ester
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| With chlorine In tetrachloromethane for 18h; Irradiation; | 100% |
| With chlorine In tetrachloromethane for 28h; Irradiation; | 97% |
| With chlorine for 33h; chlorination; | 88% |
- 207804-71-5
carbonic acid chloromethyl ester-dichloromethyl ester
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| bei der Chlorierung; |
- 101970-86-9
methyl 1,1,1-trichloromethyl carbonate
C
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| Chlorierung; |
- 101970-86-9
methyl 1,1,1-trichloromethyl carbonate
B
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| Chlorierung; |
- 101970-86-9
methyl 1,1,1-trichloromethyl carbonate
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| bei Chlorierung; | |
| durch Chlorierung; |
- 79-22-1
methyl chloroformate
- 616-38-6
carbonic acid dimethyl ester
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| vollstaendiges Chlorierung; |
- 594-42-3
chlorothio-trichloro-methane
- 32315-10-9
bis(trichloromethyl) carbonate
| Conditions | Yield |
|---|---|
| With sulfur dioxide In dichloromethane; water at 10℃; for 4h; |
- 1792-81-0
cis-1,2-cyclohexane
- 32315-10-9
bis(trichloromethyl) carbonate
- 4389-22-4, 19456-20-3, 20192-66-9
(3aR,7aS)-hexahydrobenzo[d][1,3]dioxol-2-one
| Conditions | Yield |
|---|---|
| With pyridine In dichloromethane at 20℃; | 100% |
| With pyridine In dichloromethane at -70℃; | 90% |
- 32315-10-9
bis(trichloromethyl) carbonate
- 2216-51-5
(-)-menthol
- 14602-86-9
(1R,2S,5R)-menthyl chloroformate
| Conditions | Yield |
|---|---|
| With pyridine In tetrachloromethane at 55 - 60℃; for 6h; | 100% |
| Stage #1: bis(trichloromethyl) carbonate With pyridine In toluene at 0℃; for 0.25h; Inert atmosphere; Stage #2: (-)-menthol In toluene at 20℃; for 15h; Inert atmosphere; | 100% |
| Stage #1: bis(trichloromethyl) carbonate With pyridine In toluene at 0℃; Inert atmosphere; Stage #2: (-)-menthol In toluene at 0 - 20℃; Inert atmosphere; | 100% |
| Conditions | Yield |
|---|---|
| With pyridine In dichloromethane for 2h; Ambient temperature; | 100% |
| With pyridine In dichloromethane for 1h; Ambient temperature; | |
| With pyridine In dichloromethane; ethyl acetate |
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Chemistry
Molecular Structure of Triphosgene (CAS NO.32315-10-9):
IUPAC Name: bis(trichloromethyl) carbonate
Molecular formula:: C3Cl6O3
Molecular Weight: 296.75 g/mol
H bond acceptors: 3
H bond donors: 0
Freely Rotating Bonds: 2
Polar Surface Area: 35.53Å2
Index of Refraction: 1.532
Molar Refractivity: 48.49 cm3
Molar Volume: 156.3 cm3
Surface Tension: 50.5 dyne/cm
Density: 1.898 g/cm3
Flash Point: 53.3 °C
Enthalpy of Vaporization: 44.07 kJ/mol
Boiling Point: 204.5 °C at 760 mmHg
Vapour Pressure: 0.263 mmHg at 25°C
Melting point: 78-82 °C
Storage temp: 2-8°C
Water Solubility: practically insoluble
Sensitive: Moisture Sensitive
BRN: 1787583
Product Categories: Other Reagents
Production
Triphosgene (CAS NO.32315-10-9) is prepared by exhaustive chlorination of dimethyl carbonate. The preparing process is the chlorination of methyl carbonate in the presence of fluorescence, ultraviolet ray and mixed medium and low temperature initiator in the amount of not more than 2 % of the material. The whole chlorination is completed in three stages at 15-50 deg.c, 50-70 deg.c and 70-90 deg.c separately. The said technological process obtains product of high purity and smelting point of 80-83 deg.c at a yield over 90 %.
Safety Profile
Hazard Codes: 
T+,
Xn
Risk Statements: 26-34-29-36/37/38-20/21/22
R26:Very toxic by inhalation.
R34:Causes burns.
R29:Contact with water liberates toxic gas.
R36/37/38:Irritating to eyes, respiratory system and skin.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
Safety Statements: 36/37/39-45-9-26-36-7/9
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S9:Keep container in a well-ventilated place.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
S7:Keep container tightly closed.
RIDADR: UN 2928 6.1/PG 2
WGK Germany: 2
F: 10-19-21
HazardClass: 6.1
PackingGroup: II
HS Code: 29209010
Specification
Triphosgene , with CAS number of 32315-10-9, can be called Bis(trichloromethyl)carbonate ; Bis(trichloromethyl) carbonate ; Methanol, trichloro-, carbonate(2:1) (9CI) ; Carbonicacid, bis(trichloromethyl) ester (6CI,8CI) . It is a white solid. Triphosgene (CAS NO.32315-10-9) is a chemical compound that is used as a safer substitute for phosgene, because at room temperature it is a solid crystal, as opposed to phosgene which is a gas, the crystals decompose at around 130 °C, although, the decomposition temperature of impure samples can be much lower. It is used in organic synthesis to bond one carbonyl group to two alcohols, as in the synthesis of octalactin B.