CAS 31796-55-1
:L-Alanine-4-nitroanilide hydrochloride
Description:
L-Alanine-4-nitroanilide hydrochloride is a chemical compound characterized by its structure, which includes an alanine amino acid moiety linked to a 4-nitroaniline group. This compound typically appears as a crystalline solid and is soluble in water, making it suitable for various biochemical applications. It is often used as a substrate in enzymatic assays, particularly for the detection of certain enzymes due to its ability to undergo hydrolysis, releasing detectable products. The presence of the nitro group in the aniline portion contributes to its electronic properties, influencing its reactivity and interaction with biological systems. As a hydrochloride salt, it is stabilized in its ionic form, enhancing its solubility and stability in aqueous solutions. Safety data sheets indicate that, like many nitro compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, L-Alanine-4-nitroanilide hydrochloride serves as a valuable tool in biochemical research and analytical chemistry.
Formula:C9H12ClN3O3
InChI:InChI=1/C9H11N3O3.ClH/c1-6(10)9(13)11-7-2-4-8(5-3-7)12(14)15;/h2-6H,10H2,1H3,(H,11,13);1H
InChI key:InChIKey=YEXRLSXNWLNHQR-RGMNGODLSA-N
SMILES:N(C([C@H](C)N)=O)C1=CC=C(N(=O)=O)C=C1.Cl
Synonyms:- <span class="text-smallcaps">L</span>-Alanine-4-nitroanilide hydrochloride
- <span class="text-smallcaps">L</span>-Alanine-p-nitroanilide hydrochloride
- H-Ala-Pna Hcl
- H-Ala-pNA・HCl
- L-Alanine-4-nitroanilidehydrochloride
- L-Alanine-p-nitroanilide hydrochloride
- Propanamide, 2-amino-N-(4-nitrophenyl)-, hydrochloride (1:1), (2S)-
- Propanamide, 2-amino-N-(4-nitrophenyl)-, monohydrochloride, (2S)-
- Propanamide,2-amino-N-(4-nitrophenyl)-, monohydrochloride, (2S)- (9CI)
- Propanamide,2-amino-N-(4-nitrophenyl)-, monohydrochloride, (S)-
- Propionanilide, 2-amino-4′-nitro-, monohydrochloride, <span class="text-smallcaps">L</span>-
- Propionanilide,2-amino-4'-nitro-, monohydrochloride, L- (8CI)
- L-Alanine-4-nitroanilide hydrochloride
- Propionanilide, 2-amino-4′-nitro-, monohydrochloride, L-
- [(2S)-1-(4-nitroanilino)-1-oxopropan-2-yl]azanium
- (S)-2-amino-N-(4-nitrophenyl)propionamide hydrochloride
- 2-amino-N-(4-nitrophenyl)propanamide hydrochloride
- (S)-2-AMino-N-(4-nitrophenyl)propanaMide hydrochloride
- ALANINE-P-NITROANILIDE HYDROCHLORIDE
- L-Ala-pNA·HCl
- (2S)-2-amino-N-(4-nitrophenyl)propanamide hydrochloride
- ALANINE-PNA HCL
- N~1~-(4-nitrophenyl)alaninamide hydrochloride
- L-Alanine 4-nitroanilide hydrochloride≥ 99% (HPLC)
- ALA-PNA, HCL
- L-2-AMINO-4'-NITROPROPIONANILIDE HYDROCHLORIDE
- H-ALA-PNA HCL USP/EP/BP
- L-Alanine4-nitroanilidehydrochloride,98%
- H-L-ALA-PNA HCL
- See more synonyms
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Found 7 products.
L-Alanine 4-nitroanilide hydrochloride, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C9H12ClN3O3Purity:98%Molecular weight:245.66H-Ala-pNA · HCl
CAS:Substrate for membrane alanyl aminopeptidase.Formula:C9H11N3O3·HClPurity:> 99%Color and Shape:Light YellowMolecular weight:245.7Propanamide, 2-amino-N-(4-nitrophenyl)-, monohydrochloride, (2S)-
CAS:Formula:C9H12ClN3O3Purity:99%Color and Shape:SolidMolecular weight:245.6629L-Alanine 4-nitroanilide hydrochloride
CAS:L-Alanine 4-nitroanilide hydrochlorideColor and Shape:PowderMolecular weight:245.66g/molL-Alanine 4-nitroanilide hydrochloride
CAS:<p>Please enquire for more information about L-Alanine 4-nitroanilide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C9H12ClN3O3Molecular weight:245.67 g/molL-Alanine 4-nitroanilide hydrochloride
CAS:<p>L-alanine 4-nitroanilide hydrochloride (H-Ala-pNAHCl) functions as a substrate for L-alanine aminopeptidase, an enzyme found in bacterial cell walls that catalyzes the cleavage of L-alanine from peptides. Notably, significant activity of L-alanine aminopeptidase is specific to gram-negative microbes. Thus, the utilization of H-Ala-pNAHCl can provide evidence for distinguishing between gram-positive and gram-negative organisms. When acted upon by L-alanine aminopeptide, it undergoes cleavage into L-alanine and 4-nitroanine, with the latter compound causing bacterial suspensions to exhibit a yellow coloration.</p>Formula:C9H11N3O3•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:245.66 g/mol





