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443-79-8

  • Product NameDL-Isoleucine
  • Molecular FormulaC6H13NO2
  • Molecular Weight131.175
  • Purity99%
  • Appearancewhite powder
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Product Details

Quick Details

  • CasNo: 443-79-8
  • Molecular Formula: C6H13NO2
  • Appearance: white powder
  • Purity: 99%

Chinese Manufacturer Supply 99% Pure DL-Isoleucine 443-79-8 Fast Shipping

  • Molecular Formula:C6H13NO2
  • Molecular Weight:131.175
  • Appearance/Colour:white powder 
  • Vapor Pressure:0.0309mmHg at 25°C 
  • Melting Point:210 °C 
  • Refractive Index:1.462 
  • Boiling Point:225.8 °C at 760 mmHg 
  • Flash Point:90.3 °C 
  • PSA:63.32000 
  • Density:1.035 g/cm3 
  • LogP:1.14470 
  • IDLH:1422 
  • IDLH:10127 
  • IDLH:3295 

DL-Isoleucine(Cas 443-79-8) Usage

DL-Isoleucine is an essential branched-chain amino acid crucial for protein synthesis and muscle repair. Its branched structure distinguishes it as a key component in the trio of branched-chain amino acids (BCAAs), alongside leucine and valine. Vital for growth and muscle development, DL-Isoleucine aids in maintaining a healthy metabolism. Additionally, it plays a role in regulating blood sugar levels and acts as an energy source during prolonged exercise, especially beneficial for endurance athletes.

Found abundantly in protein-rich foods like meat, dairy, eggs, and legumes, DL-Isoleucine is also available as a dietary supplement. This is particularly relevant for individuals, such as athletes, seeking to enhance muscle health and performance. However, caution is advised, and consultation with healthcare professionals is recommended before incorporating DL-Isoleucine supplements into one's routine. Overall, DL-Isoleucine's significance in protein synthesis and muscle metabolism positions it as a vital element in discussions about sports nutrition and muscle development.

InChI:InChI=1/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)

443-79-8 Relevant articles

Rational engineering ofAcinetobacter tandoiiglutamate dehydrogenase for asymmetric synthesis ofl-homoalanine through biocatalytic cascades

Diao, Shiqing,Jiang, Shuiqin,Liu, Yan,Sun, Yangyang,Wang, Hualei,Wang, Liuzhu,Wei, Dongzhi

, p. 4208 - 4215 (2021/06/30)

l-Homoalanine, a useful building block f...

Optical resolution of DL-valine, DL-leucine, and DL-isoleucine by formation of adduct with L-phenylalanine.

T Shiraiwa, A Ikawa, K Sakaguchi

Bulletin of the Chemical Society of Japan

An alkaline solution containing L-phenylalanine (L-Phe) and one of DL-valine, DL-leucine, and DL-isoleucine is allowed to selectively form a precipitate composed of L-Phe and the …

Biocatalytic asymmetric synthesis of unnatural amino acids through the cascade transfer of amino groups from primary amines onto keto acids

Park, Eul-Soo,Dong, Joo-Young,Shin, Jong-Shik

, p. 3538 - 3542 (2014/01/06)

Flee to the hills: An unfavorable equili...

443-79-8 Process route

DL-isoleucyl-leucyl anhydride
91741-17-2

DL-isoleucyl-leucyl anhydride

sulfuric acid
7664-93-9

sulfuric acid

isoleucine
319-78-8,443-79-8,1509-34-8,1509-35-9,3107-04-8,7004-09-3,73-32-5,959215-79-3,18875-42-8

isoleucine

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

LEUCINE

Conditions
Conditions Yield
Hydrolysis;
 
2-oxo-3(RS)-methylvaleric acid
1460-34-0

2-oxo-3(RS)-methylvaleric acid

isoleucine
319-78-8,443-79-8,1509-34-8,1509-35-9,3107-04-8,7004-09-3,73-32-5,959215-79-3,18875-42-8

isoleucine

Conditions
Conditions Yield
With iron sulfide; ammonium carbonate; In water; at 100 ℃; for 144h; Yield given;
 
With α-transaminase;
 
With phenylglycin; In water; acetonitrile; for 24h; Inert atmosphere; Reflux;
 
With ammonium hydroxide; D-glucose; glucose dehydrogenase from Bacillus megaterium; Acinetobacter tandoii glutamate dehydrogenase; NADH; In aq. buffer; at 30 ℃; pH=9.5; Reagent/catalyst; Enzymatic reaction;
 

443-79-8 Upstream products

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    2-Azido-3-methyl-pentanoic acid

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    2-oxo-3(RS)-methylvaleric acid

443-79-8 Downstream products

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    2-Methylbutyraldehyde

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    73-32-5

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    921-48-2

    1-chloro-2-methylbutanecarboxylic acid

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