516-06-3

  • Product NameDL-Valine
  • Molecular FormulaC5H11NO2
  • Molecular Weight117.148
  • Purity99%
  • AppearanceWhite crystalline powder
Inquiry

Product Details

Quick Details

  • CasNo: 516-06-3
  • Molecular Formula: C5H11NO2
  • Appearance: White crystalline powder
  • Purity: 99%

Food Additive DL-Valine 516-06-3 Crystalline Powder

  • Molecular Formula:C5H11NO2
  • Molecular Weight:117.148
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:0.0633mmHg at 25°C 
  • Melting Point:283.5 - 285 °C 
  • Refractive Index:1.461 
  • Boiling Point:213.642 °C at 760 mmHg 
  • PKA:pK1:2.32(+1);pK2:9.61(0) (25°C) 
  • Flash Point:83.008 °C 
  • PSA:63.32000 
  • Density:1.064 g/cm3 
  • LogP:0.75460 

DL-Valine(Cas 516-06-3) Usage

Chemical Properties

White crystalline powder

Occurrence

Reported found in many fruits, plants and animal tissues; in milk and dairy products.

Preparation

By the action of ammonia on α-bromoisovaleric acid; also through a hydantoin intermediate.

Definition

ChEBI: A branched-chain amino acid that consists of glycine in which one of the hydrogens attached to the alpha-carbon is substituted by an isopropyl group.

Use DL-Valine promotes muscle growth and tissue repair. L-valine helps build muscle by bringing more glucose to the muscles as they are stressed and worked.

InChI:InChI=1/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)

516-06-3 Relevant articles

Poly (DL-valine) electro-polymerized carbon nanotube paste sensor for determination of antihistamine drug cetirizine

T Girish, JG Manjunatha, PA Pushpanjali…

Journal of Electrochemical Science and Engineering, Vol. 11 No. 1, 2021.

Poly (DL-valine) modified multiwalled carbon nanotube paste sensor (PVLMCNTPS) was prepared by electro-polymerization route.

Regioselective Synthesis, Structure, and Chemosensitizing Antitumor Activity of Cyclic Hydroxamic Acid Based on DL-Valine

I. V. Vystorop, G. V. Shilov, A. V. Chernyak, E. N. Klimanova, T. E. Sashenkova, S. G. Klochkov, M. E. Neganova, Yu. R. Aleksandrova, U. Yu. Allayarova & D. V. Mishchenko

Russian Journal of Bioorganic Chemistry volume 47, pages757–764 (2021)

The reaction of DL-valine hydroxamic acid with triacetonamine proceeds as the N,N'-regioselective condensation to form (±)-1-hydroxy-3-isopropyl-7,7,9,9-tetramethyl-1,4,8-triazaspiro[4,5]decan-2-one.

516-06-3 Process route

hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

rac-Pro-OH
609-36-9,25191-13-3,37159-97-0,4305-67-3,4607-28-7

rac-Pro-OH

D,L-valine
516-06-3,25609-85-2,7004-03-7,921-10-8

D,L-valine

?Tyr
556-02-5,556-03-6,34537-57-0,55520-40-6,96946-98-4,60-18-4,18875-48-4,25619-78-7,30704-25-7

?Tyr

LEUCINE
328-39-2,21675-61-6,25248-98-0,70-45-1

LEUCINE

Trp
54-12-6,27732-43-0,80206-30-0,27813-82-7

Trp

Conditions
Conditions Yield
UV-Licht.Irradiation;
 
xenoamicin A
1531602-01-3

xenoamicin A

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

D-Alanine

D-allo-threonine
24830-94-2,134357-96-3,7013-32-3,82822-12-6

D-allo-threonine

(R)-leucine
328-38-1,21675-61-6,25248-98-0,70-45-1

(R)-leucine

L-isoleucine
73-32-5,959215-79-3,18875-42-8

L-isoleucine

D,L-valine
516-06-3,25609-85-2,7004-03-7,921-10-8

D,L-valine

<i>L</i>-proline
147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7

L-proline

Conditions
Conditions Yield
With hydrogenchloride; water; at 110 ℃; for 16h; High pressure;
 

516-06-3 Upstream products

  • 412011-37-1
    412011-37-1

    4-isopropylidene-2-thioxo-thiazolidin-5-one

  • 921-08-4
    921-08-4

    2-chloro-3-methylbutanoic acid

  • 10323-40-7
    10323-40-7

    2-bromoisovaleric acid

  • 4431-61-2
    4431-61-2

    2-isopropyl-malonamic acid

516-06-3 Downstream products

  • 78-84-2
    78-84-2

    isobutyraldehyde

  • 99977-10-3
    99977-10-3

    N-[2]piperidylidene-valine

  • 2816-12-8
    2816-12-8

    4-isopropyl-2,5-oxazolidinedione

  • 143896-77-9
    143896-77-9

    N-butyrylvaline

;

Relevant Products