ChemicalBook--->CAS DataBase List--->942518-29-8

942518-29-8

942518-29-8 Structure

942518-29-8 Structure
IdentificationBack Directory
[Name]

4-Azido-L-homoalanine, (S)-2-Amino-4-azidobutanoic acid hydrochloride
[CAS]

942518-29-8
[Synonyms]

H-Dab(N3).HCl
H-L-Aha-OH*HCl
L-Dab(N3)-OH·HCl
H-L-Aha-OH hydrochloride
L-Azidohomoalanine (AHA)
L-Azidohomoalanine hydrochloride
4-Azido-L-homoalanine hydrochloride
(S)-2-Amino-4-azido-butanoic acid HCl
(2S)-2-Amino-4-azido-butanoic acid HCl
(S)-2-Amino-4-azidobutanoic acid hydrochloride
Nγ-Azido-L-2,4-diaminobutyric acid hydrochloride
(2S)-2-Amino-4-azidobutanoic acid hydrochloride (1:1)
Butanoic acid, 2-amino-4-azido-, hydrochloride , (2S)-
Nγ-Azido-L-2,4-diaminobutyric acid hydrochloride≥ 99% (Titration)
4-Azido-L-homoalanine, (S)-2-Amino-4-azidobutanoic acid hydrochloride
[Molecular Formula]

C4H9ClN4O2
[MDL Number]

MFCD13184931
[MOL File]

942518-29-8.mol
[Molecular Weight]

180.59
Chemical PropertiesBack Directory
[Melting point ]

139°C
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO
[form ]

powder or crystals
[color ]

White to off-white
[Appearance]

white to light beige powder
[Water Solubility ]

Soluble to 100 mM in water
[InChI]

1S/C4H8N4O2.ClH/c5-3(4(9)10)1-2-7-8-6;/h3H,1-2,5H2,(H,9,10);1H/t3-;/m0./s1
[InChIKey]

MHHYJRIDKLZZEO-DFWYDOINSA-N
[SMILES]

[Cl-].[N+H3][C@@H](CCN=[N+]=[N-])C(=O)O
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS02
[Signal word ]

Danger
[Hazard statements ]

H242
[Precautionary statements ]

P210-P234-P235-P240-P370+P378-P403
[WGK Germany ]

WGK 3
[HS Code ]

2922498590
[Storage Class]

5.2 - Organic peroxides and self-reacting hazardous materials
[Hazard Classifications]

Self-react. C
Hazard InformationBack Directory
[Description]

L-Azidohomoalanine (AHA) is a noncanonical amino acid analog of methionine that contains an azide moiety. AHA-labeling is a fast, sensitive, non-toxic, and non-radioactive alternative to the traditional technique for detecting nascent protein synthesis.


AHA is the cell-permeable compound randomly incorporated into synthesizing protein instead of methionine during translation. The resulting azide-labeled full-length proteins can be detected via copper-catalyzed click reaction (with fluorescent or biotin-labeled alkynes) or copper-free click reaction (with cycloalkynes) and used for subsequent microscopic imaging or purification tasks.

[Chemical Properties]

White crystalline powder
[Uses]

L-Azidohomoalanine (AHA) is an amino acid analog of methionine that contains a very small modification, specifically an azido moiety. This compound can be fed to cultured cells and incorporated into proteins during active protein synthesis. Detection utilizes the chemoselective ligation or “click ” reaction between an azide and an alkyne or cyclooctyne. For example the azido-modified protein can be detected with either fluorescent alkyne or biotin alkyne. Detection sensitivity with these reagents in 1-D gels and Western blots is in the low femtomole range and compatible with downstream LC-MS/MS and MALDI-MS analysis.
[reaction suitability]

reaction type: click chemistry
[IC 50]

Alkyl-Chain
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

4-Azido-L-homoalanine, (S)-2-Amino-4-azidobutanoic acid hydrochloride(942518-29-8)1HNMR
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