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4-Azido-L-phenylalanine hydrochloride
CAS No. 34670-43-4
4-Azido-L-phenylalanine hydrochloride( p-Azidophenylalanine hydrochloride,p-Azido-L-phenylalanine hydrochloride )
Catalog No. M22484 CAS No. 34670-43-4
4-Azido-L-phenylalanine hydrochloride is an unnatural amino acid. It is used as an effective vibrational reporter of local protein environments.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 68 | In Stock |
|
| 500MG | 212 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name4-Azido-L-phenylalanine hydrochloride
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NoteResearch use only, not for human use.
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Brief Description4-Azido-L-phenylalanine hydrochloride is an unnatural amino acid. It is used as an effective vibrational reporter of local protein environments.
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Description4-Azido-L-phenylalanine hydrochloride is an unnatural amino acid. It is used as an effective vibrational reporter of local protein environments.In cell-free protein synthesis (CFPS) method, 0.9-1.7 mg/mL of modified soluble super-folder green fluorescent protein (sfGFP) containing either 4-Azido-L-phenylalanine or p-propargyloxy-l-phenylalanine (pPaF) accumulate in the CFPS solutions.
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In VitroIn cell-free protein synthesis (CFPS) method, 0.9-1.7 mg/mL of modified soluble super-folder green fluorescent protein (sfGFP) containing either 4-Azido-L-phenylalanine or p-propargyloxy-l-phenylalanine (pPaF) accumulate in the CFPS solutions.
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In Vivo——
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Synonymsp-Azidophenylalanine hydrochloride,p-Azido-L-phenylalanine hydrochloride
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number34670-43-4
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Formula Weight242.66
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Molecular FormulaC9H11ClN4O2
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Purity>98% (HPLC)
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SolubilityDMSO:103.3 mg/mL (425.70 mM);H2O:4.55 mg/mL (18.75 mM; Need ultrasonic)
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SMILESCl.N[C@@H](Cc1ccc(cc1)N=[N+]=[N-])C(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Albayrak C, et al. Cell-free co-production of an orthogonal transfer RNA activates efficient site-specific non-natural amino acid incorporation. Nucleic Acids Res. 2013 Jun;41(11):5949-63.
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