| Identification | Back Directory | [Name]
TRIMETHYLOLPROPANE MONOALLYL ETHER | [CAS]
682-11-1 | [Synonyms]
trimethylolpropaneallylether
HEXAGLYCERINE MONOALLYL ETHER
TRIMETHYLOLPROPANE ALLY ETHER
1-(Allyloxy)butane-2,2-dimethanol
TRIMETHYLOLPROPANE MONOALLYL ETHER
TriMethylolpropane Moloallyl ether
TriMethylolpropane allyl ether 98%
2-allyloxymethyl-2-ethylpropanediol
2,2-Di(hydroxymethyl)butylallyl ether
Trimethylolpropane mono allyl ether,98%
ether,allyl(2,2-bis(hydroxymethyl)butyl)
1,1,1-TRIMETHYLOLPROPANE MONOALLYL ETHER
2-(ALLYLOXYMETHYL)-2-ETHYL-1,3-PROPANEDIOL
2,2-(dihydroxymethyl)-1-butanomonoallylether
2-Ethyl-2-[(allyloxy)methyl]-1,3-propanediol
2-ethyl-2-[(2-propenyloxy)methyl]-3-propanediol
1,1,1-(TRIHYDROXYMETHYL)PROPANE MONOALLYL ETHER
2-ETHYL-2-[(PROPENYLOXY)METHYL]-1,3-PROPANEDIOL
3-Propanediol,2-ethyl-2-[(2-propenyloxy)methyl]-1
1,3-Propanediol, 2-ethyl-2-(2-propenyloxy)methyl-
2-ethyl-2-[(2-propenyloxy) methyl]-1,3-Propanediol
2-ETHYL-2-(HYDROXYMETHYL)-1,3-PROPANEDIOL MONO ALLYL ETHER | [EINECS(EC#)]
211-662-7 | [Molecular Formula]
C9H18O3 | [MDL Number]
MFCD00046753 | [MOL File]
682-11-1.mol | [Molecular Weight]
174.24 |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS VISCOUS LIQUID | [Melting point ]
-10 °C
| [Boiling point ]
160 °C33 mm Hg(lit.)
| [density ]
1.01 g/mL at 25 °C(lit.)
| [vapor pressure ]
0.035Pa at 25℃ | [refractive index ]
n20/D 1.467(lit.)
| [Fp ]
>230 °F
| [form ]
viscous liquid | [pka]
14.25±0.10(Predicted) | [Specific Gravity]
1.01 | [Water Solubility ]
10g/L at 20℃ | [Hydrolytic Sensitivity]
4: no reaction with water under neutral conditions | [InChI]
InChI=1S/C9H18O3/c1-3-5-12-8-9(4-2,6-10)7-11/h3,10-11H,1,4-8H2,2H3 | [InChIKey]
LZDXRPVSAKWYDH-UHFFFAOYSA-N | [SMILES]
C(O)C(CC)(COCC=C)CO | [LogP]
1.4 at 20℃ | [EPA Substance Registry System]
1,3-Propanediol, 2-ethyl-2-[(2-propenyloxy)methyl]- (682-11-1) |
| Questions And Answer | Back Directory | [Uses]
Trimethylpropane monoallyl ester is an aliphatic polycarbonate, an important class of biodegradable/absorbable polymers. It possesses a wide range of physical, chemical, and biological properties, and comes in many varieties with tunable structures to meet diverse biomedical needs. Furthermore, the degradation of polycarbonates produces carbon dioxide and neutral diols, avoiding the adverse effects caused by carboxylic acids produced during the degradation of polylactic acid (PLA) and polyglycolic acid (PGA). Biodegradable polycarbonates are finding increasingly widespread applications in absorbable surgical sutures, controlled drug release, in vivo implant materials, and tissue regeneration. Trimethylpropane monoallyl ester can also be used as a pharmaceutical synthesis intermediate. |
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