CUCURBIT(8)URIL manufacturers
- CUCURBIT(8)URIL
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- $1.10
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2026-08-20
- CAS:259886-51-6
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
- Cucurbit[8]uril
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- $41.00
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2026-07-15
- CAS:259886-51-6
- Purity: 98.74%
- Supply Ability: 10g
- CUCURBIT(8)URIL
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2026-06-30
- CAS:259886-51-6
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1000kg
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| | CUCURBIT(8)URIL Basic information |
| Product Name: | CUCURBIT(8)URIL | | Synonyms: | Curcubit[8]uril;Cucurbit[8]uril (CB[8]) hydrate, 99+%;Cucurbit[8]uril hydrate contains acid of crystalization;Cucurbit[8]uril hydrate
;2,20:3,19-Dimethano-2,3,4a,5a,6a,7a,8a,9a,10a,11a,12a,13a,14a,15a,16a,17a,19,20,21a,22a,23a,24a,25a,26a,27a,28a,29a,30a,31a,32a,33a,34a-dotriacontaazabispentaleno[1''''',6''''':5'''',6'''',7'''']cycloocta[1'''',2'''',3'''':3''',4''']pentaleno[1''',6''':5';Cucurbit[8]uril (CB[8]) hydrate;2,20:3,19-Dimethano-2,3,4a,5a,6a,7a,8a,9a,10a,11a,12a,13a,14a,15a,16a,17a,19,20,21a,22a,23a,24a,25a,26a,27a,28a,29a,30a,31a,32a,33a,34a-dotriacontaazabispentaleno[1''''',6''''':5'''',6'''',7'''']cycloocta[1'''',2'''',3'''':3''',4''']pentaleno[1''',6''':5'',6'',7'']cycloocta[1'',2'',3'':3',4']pentale...;CUCURBIT(8)URIL ISO 9001:2015 REACH | | CAS: | 259886-51-6 | | MF: | C48H48N32O16 | | MW: | 1329.1 | | EINECS: | | | Product Categories: | Amine-Functional Polymers;Hydrophilic Polymers;Polymer Science;API | | Mol File: | 259886-51-6.mol |  |
| | CUCURBIT(8)URIL Chemical Properties |
| density | 2.71 | | storage temp. | Inert atmosphere,Room Temperature | | form | solid | | color | white | | Optical Rotation | [α]20/D -61°, c =1% in H2O | | Cosmetics Ingredients Functions | FILM FORMING CHELATING EMULSION STABILISING ABSORBENT | | InChIKey | COYIBPCTQSGIKE-IIKCYMFNSA-N |
| WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | CUCURBIT(8)URIL Usage And Synthesis |
| Uses | Cucurbit[8]uril hydrate can be used as ananocontainer in a polyelectrolyte multilayer film. | | Definition | ChEBI: Cucurbit[8]uril is a cucurbituril. | | Synthesis | General procedure for the synthesis of cucurbit[n]uril from glyburide and diethoxymethane: Unsubstituted glyburide (19.94 g) and pure methanesulfonic acid (82 mL) were added to a reaction flask and heated to 80 °C. Subsequently, diethoxymethane (35.21 mL) was added slowly and the reaction mixture was warmed up to 100 °C (internal temperature) and kept for 18 hours. Upon completion of the reaction, the mixture was cooled and poured into acetone (410 mL) and a brown powder was precipitated. The product composition was analyzed by 1H NMR to give cucurbit[5]uril (8%), cucurbit[6]uril (42%), cucurbit[7]uril (43%), cucurbit[8]uril (7%), cucurbit[9]uril (0%), cucurbit[10]uril (0%) and cucurbit[13]uril (0%). In addition, the residual formaldehyde content was 34 ppm by HPLC. | | in vivo | Cucurbit[8]uril shows a very low toxicity of the in vivo intravenous injection, as well as oral administration studies on mice[2]. | | References | [1] Patent: WO2018/115822, 2018, A1. Location in patent: Page/Page column 16 |
| | CUCURBIT(8)URIL Preparation Products And Raw materials |
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