Fmoc-Asn(Trt)-OH
ALDRICH/47672 - ≥97.0%
Synonym: Nα-(9-Fluorenylmethoxycarbonyl)-Nγ-trityl-L-asparagine; Nα-Fmoc-Nγ-trityl-L-asparagine
CAS Number: 132388-59-1
Empirical Formula (Hill Notation): C38H32N2O5
Molecular Weight: 596.67
MDL Number: MFCD00077049
Linear Formula: C38H32N2O5
Product Type: Chemical
application(s) | peptide synthesis |
assay | ≥97.0% |
form | powder |
functional group | Fmoc |
InChI | 1S/C38H32N2O5/c41-35(40-3 |
InChI key | KJYAFJQCGPUXJY-UMSFTDKQSA |
mp | 201-204 °C (lit.) |
optical activity | [α]20/D −15.0±1°, c = 1% in methanol |
reaction suitability | reaction type: Fmoc solid-phase peptide synthesis |
SMILES string | OC(=O)[C@H](CC(=O)NC(c1cc |
storage temp. | 2-8°C |
Application: | Fmoc-Asn(Trt)-OH has been used to synthesize peptides on cellulose membrane by SPOT method |
General description: | Fmoc-Asn(Trt)-OH has good solubility properties in most organic solvents, and its use has been shown to result in significantly purer peptides than other derivatives used for the introduction of Asn [1, 2]. Coupling can be performed by standard procedures. The trityl group is normally removed by 95% TFA in 1-3 hours, with no alkylation of Trp residues. When Asn(Trt) is the N-terminal residue, the reaction time may need to be extended to ensure complete deprotection [3]. |
Packaging: | 1 kg in poly bottle |
Packaging: | 5, 25, 100 g in poly bottle |
Symbol | GHS09 |
Hazard statements | H411 |
Risk Statements | 53 |
Safety Statements | 61 |
RIDADR | UN 3077 9 / PGIII |
WGK Germany | WGK 2 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | ≥97.0% |
mp | 201-204 °C (lit.) |
Storage Temp. | 2-8°C |
UNSPSC | 12352209 |