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| N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Basic information |
| Product Name: | N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL | | Synonyms: | 1,1-DINEOPENTYLOXYTRIMETHYLAMINE;1,1-bis(2,2-dimethylpropoxy)-N,N,N-trimethylamine;Methanamine, 1,1-bis(2,2-dimethylpropoxy)-N,N-dimethyl-;1,1-dineopentyloxy-n,n-dimethylmethylamine;N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL;N,N-Dimethyl[bis(neopentyloxy)]methanamine;Dimethylformamide dineopentyl acetal.;N,N-Dimethylformamide Dineopentyl Acetal [for Esterification] | | CAS: | 4909-78-8 | | MF: | C13H29NO2 | | MW: | 231.37 | | EINECS: | 225-536-4 | | Product Categories: | Analytical Chemistry;Esterification & Alkylation (GC Derivatizing Reagents);GC Derivatizing Reagents;N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents) | | Mol File: | 4909-78-8.mol |
| N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Chemical Properties |
| Melting point | 253.5℃ | | Boiling point | 85-87 °C/10 mmHg (lit.) | | density | 0.829 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.412(lit.) | | Fp | 125 °F | | storage temp. | Store at 0-5°C | | pka | 5.24±0.50(Predicted) | | form | clear liquid | | color | Colorless to Almost colorless | | Water Solubility | Hydrolyzes with water. | | Sensitive | Moisture Sensitive | | BRN | 741992 | | CAS DataBase Reference | 4909-78-8(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | RIDADR | 1993 | | WGK Germany | 3 | | F | 9-21 | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29110000 |
| N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Usage And Synthesis |
| Chemical Properties | Colorless to slight yellow liquid | | Uses | N,N-Dimethylformamide dineopentyl acetal helps in the lactonization of ω-hydroxyacids, giving lactones of up to 16-membered rings. It can be used to convert primary alcohols to alkylating agents for use in the alkylation of thiols. It is used in the esterification of Nα-9-fluorenylmethyloxycarbonylamino acids. It was used in the synthesis of 1,3-dialkyl, benzyl and cyclohexyl barbiturate derivatives. It was used as reagent during the synthesis of L-serine and L-cystine stereospecifically labeled with deuterium at the β-position. |
| N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Preparation Products And Raw materials |
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