tert-Butyl Methyl Ether
![eMolecules tert-Butyl 3,6-diazabicyclo[3.1.1]heptane-3-carboxylate | A2B Chem LLC | 1251017-66-9 | MFCD17016735 | 198.266 | C10H18N2O2 | 98.000 | CC(C)(C)OC(=O)N1CC2CC(C1)N2 | 1g | 476107698](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC3715018.JPG-250.jpg)
eMolecules tert-Butyl 3,6-diazabicyclo[3.1.1]heptane-3-carboxylate | A2B Chem LLC | 1251017-66-9 | MFCD17016735 | 198.266 | C10H18N2O2 | 98.000 | CC(C)(C)OC(=O)N1CC2CC(C1)N2 | 1g | 476107698
tert-Butyl 3,6-diazabicyclo[3.1.1]heptane-3-carboxylate | A2B Chem LLC | 1251017-66-9 | MFCD17016735 | 198.266 | C10H18N2O2 | 98.000 | CC(C)(C)OC(=O)N1CC2CC(C1)N2 | 1g | 476107698
Chemscene ChemScene | tert-Butyl 3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate | 250MG | CS-0097470 | 0.98 | 148858-04-2| MFCD17170819 | 248.28
ChemScene | tert-Butyl 3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate | 250MG | CS-0097470 | 0.98 | 148858-04-2| MFCD17170819 | 248.28
Selleck Chemical LLC Vanillyl Butyl Ether S3965-25mg
Vanillyl Butyl Ether (4-(Butoxymethyl)-2-methoxyphenol) an ether of monohydroxybenzoic acid is added to food products as a flavoring agent It is also present in cosmetics and personal care products as a fragrance ingredient oral care agent hair conditioning agent and warming or cooling agent
![eMolecules Pharmablock / tert-butyl N-[2-[2-[2-[tert-butyl(dimethyl)silyl]oxyethoxy]ethylamino]ethyl]-N-methyl-carbamate / 25mg / 665627600 / PBU8141 / 0.000 / 2403639-16-5 / [null] / 376.613 / C18H40N2O4Si](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502441270.PNG-250.jpg)
eMolecules Pharmablock / tert-butyl N-[2-[2-[2-[tert-butyl(dimethyl)silyl]oxyethoxy]ethylamino]ethyl]-N-methyl-carbamate / 25mg / 665627600 / PBU8141 / 0.000 / 2403639-16-5 / [null] / 376.613 / C18H40N2O4Si
Pharmablock / tert-butyl N-[2-[2-[2-[tert-butyl(dimethyl)silyl]oxyethoxy]ethylamino]ethyl]-N-methyl-carbamate / 25mg / 665627600 / PBU8141 / 0.000 / 2403639-16-5 / [null] / 376.613 / C18H40N2O4Si
eMolecules AstaTech / TERT-BUTYL 2-(PHENYLMETHYLSULFONAMIDO)ACETATE / 0.25g / 112532090 / AR3122 / 95.000 / 1015856-04-8 / MFCD09998226 / 285.360 / C13H19NO4S
AstaTech / TERT-BUTYL 2-(PHENYLMETHYLSULFONAMIDO)ACETATE / 0.25g / 112532090 / AR3122 / 95.000 / 1015856-04-8 / MFCD09998226 / 285.360 / C13H19NO4S
Cambridge Isotope Laboratories Bisphenol F diglycidyl ether (BFDGE) (ring-13C12 99%) 100 ug/mL in acetonitrile 1 2 mL
Bisphenol F diglycidyl ether (BFDGE) (ring-13C12 99%) 100 ug/mL in acetonitrile 1 2 mL
Medchemexpress LLC Vanillyl butyl ether | 82654-98-6 | MFCD00238529 | 99.8% | 210.27 g/mol | C12H18O3 | 1 ML
Vanillyl butyl ether is an organic vanillyl derivative used in research as a mild warming and repellent agent and as a TRP channel modulator. It is supplied as a DMSO solution for laboratory use, and is provided with high purity and documented physical properties. For research use only.
Cayman Chemical CnabIgerol dImethyl ether 10mg
An analytical reference standard that is structurally similar to known phytocannabinoids; intended for research and forensic applications
Sigma Aldrich Fine Chemicals Biosciences tert Butyl methyl ether HP
tert-Butyl methyl ether is a gasoline additive. Its oxidative degradation by propane-oxidizing bacterial strains has been tested. Kinetics of its heat-assisted persulfate oxidation has been investigated at various pH temperature oxidant concentration and ionic strength levels. Its biodegradation followed a pseudo-first-order decay model and its pseudo-first-order rate constants were evaluated. MTBE can be synthesized by acid catalyzed reaction between methanol and isobutene. A study suggests that the addition of MTBE increases the number of active sites during polymerization of propene by stopped-flow method.
Sigma Aldrich Fine Chemicals Biosciences tert Butyl methyl ether su
tert-Butyl methyl ether (methyl tert-butyl ether MTBE) is a gasoline additive. Its oxidative degradation by propane-oxidizing bacterial strains has been tested. Kinetic studies of its heat-assisted persulfate oxidation at various pH temperature oxidant concentration and ionic strength levels suggests that reaction exhibits a pseudo-first-order decay model.