47672
Fmoc-Asn(Trt)-OH
≥97.0%, for peptide synthesis
Manufacturer: Sigma Aldrich
CAS Number: 132388-59-1
Synonym(S): Nα-(9-Fluorenylmethoxycarbonyl)-Nγ-trityl-L-asparagine, Nα-Fmoc-Nγ-trityl-L-asparagine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 47672-5-G | In Stock | ₹ 8,497.63 |
| 25 G | 47672-25-G | In Stock | ₹ 12,643.60 |
| 100 G | 47672-100-G | In Stock | ₹ 27,279.00 |
| 1 KG | 47672-1-KG | In Stock | ₹ 1,32,725.33 |
47672 - 5 G
In Stock
Quantity
1
Base Price: ₹ 8,497.63
GST (18%): ₹ 1,529.573
Total Price: ₹ 10,027.203
product name
Fmoc-Asn(Trt)-OH, ≥97.0%
Quality Level
100
Assay
≥97.0%
form
powder
optical activity
[α]20/D −15.0±1°, c = 1% in methanol
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
201-204 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Chem-Impex International, Inc. Na-Fmoc-Ng-trityl-L-asparagine | 132388-59-1 | MFCD00077049 | 100G | Chem-Impex International, Inc. | ₹ 15,493.20 | |
 | Chem-Impex International, Inc. Na-Fmoc-Ng-trityl-L-asparagine | 132388-59-1 | MFCD00077049 | 250G | Chem-Impex International, Inc. | ₹ 35,124.09 | |
| | Chem-Impex International, Inc. Na-Fmoc-Ng-trityl-L-asparagine | 132388-59-1 | MFCD00077049 | 25G | Chem-Impex International, Inc. | ₹ 4,521.85 | |
| | Chem-Impex International, Inc. Na-Fmoc-Ng-trityl-L-asparagine | 132388-59-1 | MFCD00077049 | 5G | Chem-Impex International, Inc. | ₹ 3,009.15 | |
 | Chemscene CS-W002327,AbaChemscene,(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanoic acid,132388-59-1,100g | Chemscene | ₹ 6,417.00 | |
 | FMOC-Asn(Trt)-OH | Sigma Aldrich | ₹ 6,809.99 - ₹ 43,670.00 | |
 | Fmoc-Asn(Trt)-OH | ChemScene | ₹ 855.60 - ₹ 63,057.72 |
Related Products
Description
- 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].
- Application: Fmoc-Asn(Trt)-OH has been used to synthesize peptides on cellulose membrane by SPOT method[1]
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product name: Fmoc-Asn(Trt)-OH, ≥97.0%
Quality Level: 100
Assay: ≥97.0%
form: powder
optical activity: [α]20/D −15.0±1°, c = 1% in methanol
reaction suitability: reaction type: Fmoc solid-phase peptide synthesis
mp: 201-204 °C (lit.)
application(s): peptide synthesis
functional group: Fmoc
storage temp.: 2-8°C
product name:
Fmoc-Asn(Trt)-OH, ≥97.0%
Quality Level:
100
Assay:
≥97.0%
form:
powder
optical activity:
[α]20/D −15.0±1°, c = 1% in methanol
reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis
mp:
201-204 °C (lit.)
application(s):
peptide synthesis
functional group:
Fmoc
storage temp.:
2-8°C
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form: powder
optical activity: [α]/D -14.0±1.5°, c = 1% in DMF
reaction suitability: reaction type: Fmoc solid-phase peptide synthesis
mp: __
application(s): peptide synthesis
functional group: Fmoc
storage temp.: 2-8°C
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100
Assay:
≥98.0% (HPLC)
form:
powder
optical activity:
[α]/D -14.0±1.5°, c = 1% in DMF
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reaction type: Fmoc solid-phase peptide synthesis
mp:
__
application(s):
peptide synthesis
functional group:
Fmoc
storage temp.:
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__
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100
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≥99.0% (GC)
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