L-Norvaline

Basic information

  • Product Name:L-Norvaline
  • CasNo.:6600-40-4
  • MF:C5H11NO2
  • MW:117.148

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:>300 °C(lit.)
  • Packing:white to light yellow crystal powder
  • Throughput:
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Product Details

CasNo: 6600-40-4

MF: C5H11NO2

Appearance: white to light yellow crystal powder

Cost-effective customized wholesale L-Norvaline 6600-40-4

  • Molecular Formula:C5H11NO2
  • Molecular Weight:117.148
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.0366mmHg at 25°C 
  • Melting Point:>300 °C(lit.) 
  • Refractive Index:25 ° (C=10, 6mol/L HCl) 
  • Boiling Point:222.9 °C at 760 mmHg 
  • PKA:2.32(at 25℃) 
  • Flash Point:88.6 °C 
  • PSA:63.32000 
  • Density:1.067 g/cm3 
  • LogP:0.89870 

L-norvaline(Cas 6600-40-4) Usage

benefits

Some benefits with taking L-norvaline:L-Norvaline increases blood flow to working muscles, which can lead to greater muscle pumps during workouts, less soreness after workouts, and faster recovery times between workouts.L-Norvaline, an amino acids supplement for men, may support nitric oxide production in healthy individuals, where nitric oxide plays an important role in many biological processes in the body including muscular contraction, blood circulation and blood flow throughout the body.

Biochem/physiol Actions

L-Norvaline enhances NO production from activated macrophages.

Side effects

Mild gastrointestinal symptoms such as stomach irritation, nausea, and vomiting may result from L-Norvaline supplementation.

Safety

Researchers from the University of Technology Sydney found taking the amino acid L-norvaline, even in small doses, could make cells unhealthy and eventually kill them.However, in a study published in the US National Library of Medicine National Institutes of Health dated December 17, 2019, and entitled “Reports of L-Norvaline Toxicity in Humans May Be Greatly Overstated”, it was argued that the quantities of L-Norvaline used in the study claiming its toxicity was greatly above cytotoxic levels for all amino acids. Hence, it was concluded in the said study that as long as L-Norvaline is taken within recommended doses, it will not necessarily cause cytotoxic effects. A typical dose of L-Norvaline is around 100mg-250mg per day.

Purification Methods

Crystallise norvaline from aqueous EtOH or water. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2390-2399 1961, Beilstein 4 III 1331-1333, 4 IV 128, 2629.]

General Description

L-Norvaline is a non-proteinogenic amino acid with the chemical name (S)-2-aminopentanoic acid, characterized by a five-carbon side chain. It has been synthesized stereoselectively through efficient, chromatography-free methods, demonstrating its relevance in organic and bioorganic chemistry. L-norvaline's structural features, such as its side chain length, influence molecular interactions, as seen in studies on peptide nucleic acids (PNAs), where norvalyl derivatives were used to investigate pairing selectivity and stacking properties. This highlights its utility in designing modified biomolecules for applications in molecular recognition and synthetic biology.

Definition

ChEBI: L-Norvaline is a 2-aminopentanoic acid that has S-configuration. It has a role as a bacterial metabolite. It is a (R)-fenbuconazole and a 2-aminopentanoic acid. It is an enantiomer of a D-2-aminopentanoic acid. It is a tautomer of a L-2-aminopentanoic acid zwitterion.

InChI:InChI=1/C5H11NO2/c1-2-3-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1

6600-40-4 Relevant articles

Bioelectrocatalytic Conversion from N2 to Chiral Amino Acids in a H2/α-Keto Acid Enzymatic Fuel Cell

Cai, Rong,Chen, Hsiaonung,Chen, Hui,Dong, Fangyuan,Minteer, Shelley D.,Prater, Matthew B.

supporting information, p. 4028 - 4036 (2020/03/11)

Enzymatic electrosynthesis is a promisin...

Semi-rational hinge engineering: modulating the conformational transformation of glutamate dehydrogenase for enhanced reductive amination activity towards non-natural substrates

Liu, Yayun,Meng, Lijun,Wu, Jianping,Yang, Lirong,Yin, Xinjian,Zhou, Haisheng

, p. 3376 - 3386 (2020/06/09)

The active site is the common hotspot fo...

Combinatorial Mutation Analysis of ω-Transaminase to Create an Engineered Variant Capable of Asymmetric Amination of Isobutyrophenone

Kim, Hong-Gon,Han, Sang-Woo,Shin, Jong-Shik

, p. 2594 - 2606 (2019/05/15)

ω-Transaminase (ω-TA) is an important en...

Artificial Biocatalytic Cascade with Three Enzymes in One Pot for Asymmetric Synthesis of Chiral Unnatural Amino Acids

Zhou, Haisheng,Meng, Lijun,Yin, Xinjian,Liu, Yayun,Xu, Gang,Wu, Jianping,Wu, Mianbin,Yang, Lirong

supporting information, p. 6470 - 6477 (2019/11/02)

Two biocatalytic reactions, transaminati...

6600-40-4 Process route

DL-α-alanyl-DL-norvaline
1116-19-4,2325-18-0,39537-36-5,61500-92-3,95191-59-6,103067-82-9

DL-α-alanyl-DL-norvaline

L-alanin
56-41-7,25191-17-7,18875-37-1

L-alanin

D-Alanine
338-69-2,25191-17-7,18875-37-1

D-Alanine

D-norvaline
2013-12-9,498-18-0

D-norvaline

L-Norvaline
6600-40-4,498-18-0

L-Norvaline

Conditions
Conditions Yield
With (S)-1-(N,N-dimethylaminomethyl)-2-formylcymantrene; sodium methylate; copper (I) acetate; for 1h; Ambient temperature;
21.69%
39.43%
60.57%
78.31%
With (S)-1-(N,N-dimethylaminomethyl)-2-formylcymantrene; sodium methylate; copper (I) acetate; for 3h; Ambient temperature;
76.83%
23.15%
26.2%
73.8%
With (R)-1-(N,N-dimethylaminomethyl)-2-formylcymantrene; sodium methylate; copper (I) acetate; for 1h; Ambient temperature;
26.8%
57.84%
42.16%
73.2%
With (R)-1-(N,N-dimethylaminomethyl)-2-formylcymantrene; sodium methylate; copper (I) acetate; for 1h; Ambient temperature;
26.8%
73.2%
42.16%
57.84%
(2S)-[(1'R)-phenylethylamino]-4-pentenoic acid

(2S)-[(1'R)-phenylethylamino]-4-pentenoic acid

L-Norvaline
6600-40-4,498-18-0

L-Norvaline

Conditions
Conditions Yield
With hydrogen; palladium on carbon; In water; at 50 ℃; for 47h; under 16501.7 Torr;
41.5%

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