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Key Documents

21850

Sigma-Aldrich

Carbonate on polymer support

extent of labeling: ~3.5 mmol/g NaCO3- loading

Synonym(s):

Amberlite™ IRA 900 NaCO3--form

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About This Item

UNSPSC Code:
12352128
NACRES:
NA.22
Pricing and availability is not currently available.

reaction suitability

reaction type: solution phase peptide synthesis
reactivity: proton reactive

extent of labeling

~3.5 mmol/g NaCO3- loading

impurities

~20% water

Other Notes

Polymeric reagent for the conversion of alkyl halides to alcohols in an aprotic solvent [1]; Synthesis of oxazolidinones and aziridines[2]

Legal Information

Amberlite is a trademark of DuPont de Nemours, Inc.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS7547V
BCBK1765V
1380564V
1380564
1259519

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A. Bongini et al.
Journal of the Chemical Society. Perkin Transactions 1, 1339-1339 (1986)
Margaret L Eng et al.
Ecotoxicology and environmental safety, 179, 104-110 (2019-04-27)
Tetrabromobisphenol A bis(2,3-dibromopropyl) ether (TBBPA-BDBPE) is an additive flame retardant used in polyolefins and polymers. It has been detected in biota, including in avian eggs, yet little is known of its effects. We assessed the pattern of TBBPA-BDBPE concentrations in
G. Cardillo et al.
Journal of the Chemical Society. Chemical Communications, 1309-1309 (1982)
Margaret L Eng et al.
Ecotoxicology and environmental safety, 179, 151-159 (2019-04-30)
Tetrabromobisphenol A bis(2,3-dibromopropyl ether) (TBBPA-BDBPE) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTPBE) are both brominated flame retardants (BFRs) that have been detected in birds; however, their potential biological effects are largely unknown. We assessed the effects of embryonic exposure to TBBPA-BDBPE and BTBPE in
Elena Chiurchiù et al.
Molecules (Basel, Switzerland), 24(24) (2019-12-19)
Highly functionalized furans are the key scaffolds of many pharmaceuticals and bioactive natural products. Herein, we disclose a new fruitful synthesis of polyfunctionalized furans starting from β-nitroenones and α-functionalized ketones. The protocol involves two steps promoted by solid supported species

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