Name | Dibenzyl phosphite |
Synonyms | AURORA KA-1209 DIBENZYL PHOSPHITE Dibenzyl phosphite Dibenzyl phosphonate DIBENZYL PHOSPHONATE Bromine Hydride Acetic Acid dibenzyl hydrogen phosphite Phosphonic acid dibenzyl ester PHOSPHONIC ACID DIBENZYL ESTER Phosphorous acid dibenzyl ester PHOSPHOROUS ACID DIBENZYL ESTER Dibenzyl phosphite technical grade Dibenzyl PhosphonatePhosphonic Acid Dibenzyl EsterPhosphorous Acid Dibenzyl Ester |
CAS | 17176-77-1 |
EINECS | 241-226-1 |
InChI | InChI=1/C14H15O3P/c15-18(16-11-13-7-3-1-4-8-13)17-12-14-9-5-2-6-10-14/h1-10,18H,11-12H2 |
InChIKey | DYUGVWSETOTNKQ-UHFFFAOYSA-N |
Molecular Formula | C14H15O3P |
Molar Mass | 262.24 |
Density | 1.187 g/mL at 25 °C (lit.) |
Melting Point | 0 to 5° |
Boling Point | 110-120 °C/0.01 mmHg (lit.) |
Flash Point | >230°F |
Water Solubility | Soluble in DMSO, Methanol. Reacts with water. |
Solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) |
Vapor Presure | 0mmHg at 25°C |
Appearance | Transparent slightly yellow liquid |
Color | Clear colorless to yellow |
Merck | 14,3014 |
BRN | 1982794 |
Storage Condition | 2-8°C |
Sensitive | Air & Moisture Sensitive |
Refractive Index | n20/D 1.555(lit.) |
MDL | MFCD00004774 |
Physical and Chemical Properties | Colorless oily liquid. Melting Point -5-5 deg C, boiling point of 160-164 deg C (13.3) (decomposition),110-120 deg C (1.33), the relative density of 1.187, refractive index of 1.5521(18 deg C). Soluble in benzene. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
UN IDs | UN3278 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 21 |
HS Code | 29209090 |
Hazard Class | 6.1 |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
Use | Used to prepare phosphorylated amines. |
Production method | It is obtained by the reaction of benzyl alcohol and phosphorus trichloride. |