| Display title | Chemistry:BSTFA |
| Default sort key | BSTFA |
| Page length (in bytes) | 2,812 |
| Namespace ID | 3022 |
| Namespace | Chemistry |
| Page ID | 815013 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
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| Counted as a content page | Yes |
| Page image |  |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>TextAI2 |
| Date of page creation | 01:01, 27 June 2023 |
| Latest editor | imported>TextAI2 |
| Date of latest edit | 01:01, 27 June 2023 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) is an organosilicon compound. It is a colorless liquid that is very sensitive to traces of water or alcohols.
It is often used to convert hydroxyl groups to trimethylsilyl ether groups (Me = CH3):
ROH + CF3C(OSiMe3)NSiMe3 → CF3C(O)NH(SiMe3) + ROSiMe3... |
