![]() | |
Names | |
---|---|
Preferred IUPAC name
Propan-2-yl 4-hydroxybenzoate | |
Other names
Isopropyl 4-hydroxybenzoate; Isopropyl p-hydroxybenzoate
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.021.882 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H12O3 | |
Molar mass | 180.203 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Isopropylparaben is a paraben.
Isopropylparaben has been prepared via the stepwise addition of isopropanol, thionyl chloride, and p-hydroxybenzoic acid at low temperature, followed by heating the reaction mixture. [1]
![]() | |
Names | |
---|---|
Preferred IUPAC name
Propan-2-yl 4-hydroxybenzoate | |
Other names
Isopropyl 4-hydroxybenzoate; Isopropyl p-hydroxybenzoate
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.021.882 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C10H12O3 | |
Molar mass | 180.203 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Isopropylparaben is a paraben.
Isopropylparaben has been prepared via the stepwise addition of isopropanol, thionyl chloride, and p-hydroxybenzoic acid at low temperature, followed by heating the reaction mixture. [1]