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    S-BAIBA

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      S-BAIBA

      SKU
      A0147

      Category: Metabolites

      Synonyms
      L-3-Amino-isobutyric acid
      4249-19-8
      CAS-Number
      C4H9NO2
      Molecular Formula
      103.12
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥99% (TLC)
      Appearance
      White to off-white powder
      Identity
      1H-NMR

      Properties

      Solvents
      methanol
      Melting Point
      179 °C

      Documentation

      Safety Data Sheet (SDS)
      CDX A0147 MSDS.pdf
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Hazard statements
      H319
      Precautionary statements
      P305 + P351 + P338
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      Beta-Aminoisobutyric acid is a non-protein amino acid originating from the catabolism of thymine and valine. beta-Aminoisobutyric acid occurs in two isomeric forms and both enantiomers of beta-Aminoisobutyric acid can be detected in human urine and plasma. In plasma, the S-enantiomer is the predominant type due to active renal reabsorption. In contrast, urine almost exclusively contains the R-enantiomer of beta-Aminoisobutyric acid, which is eliminated both by filtration and tubular secretion. The S-enantiomer of beta-Aminoisobutyric acid is predominantly derived from the catabolism of valine, the R-enantiomer is the product of the catabolism of the pyrimidine bases uracil and thymine by the enzyme dihydropyrimidine dehydrogenase (DPD), in what constitutes the first step of the pyrimidine degradation pathway. Transient high levels of beta-Aminoisobutyric acid have been observed under a variety of pathological conditions such as lead poisoning, starvation, in total body irradiation and in a number of malignancies. Recently R-/S-enantiomer mixtures have been shown to be browning inducer of white adipose tissue.
      Smiles
      OC([C@@H](C)CN)=O
      InChi Key
      QCHPKSFMDHPSNR-VKHMYHEASA-N
      References
      (1) S. Landaas & E. Solem: Scand. J. Clin. Lab. Invest. 43, 95 (1983) , (2) F. Podebrad, et al.: Clin. Chim. Acta 292, 93 (2000) , (3) A.B. Van Kuilenburg, et al.: Biochem. J. 379, 119 (2004)
      InChi
      InChI=1S/C4H9NO2/c1-3(2-5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1

      Beta-Aminoisobutyric acid is a non-protein amino acid originating from the catabolism of thymine and valine. beta-Aminoisobutyric acid occurs in two isomeric forms and both enantiomers of beta-Aminoisobutyric acid can be detected in human urine and plasma. In plasma, the S-enantiomer is the predominant type due to active renal reabsorption. In contrast, urine almost exclusively contains the R-enantiomer of beta-Aminoisobutyric acid, which is eliminated both by filtration and tubular secretion. The S-enantiomer of beta-Aminoisobutyric acid is predominantly derived from the catabolism of valine, the R-enantiomer is the product of the catabolism of the pyrimidine bases uracil and thymine by the enzyme dihydropyrimidine dehydrogenase (DPD), in what constitutes the first step of the pyrimidine degradation pathway. Transient high levels of beta-Aminoisobutyric acid have been observed under a variety of pathological conditions such as lead poisoning, starvation, in total body irradiation and in a number of malignancies. Recently R-/S-enantiomer mixtures have been shown to be browning inducer of white adipose tissue.

      SKU: A0147 Category: Metabolites
      • Additional information

      Additional information

      Synonyms

      L-3-Amino-isobutyric acid

      Purity

      ≥99% (TLC)

      Appearance

      White to off-white powder

      CAS-Number

      4249-19-8

      Molecular Formula

      C4H9NO2

      Molecular Weight

      103.12

      Identity

      1H-NMR

      Solvents

      methanol

      Melting Point

      179 °C

      Smiles

      OC([C@@H](C)CN)=O

      InChi Key

      QCHPKSFMDHPSNR-VKHMYHEASA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Hazard statements

      H319

      Precautionary statements

      P305 + P351 + P338

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) S. Landaas & E. Solem: Scand. J. Clin. Lab. Invest. 43, 95 (1983), (2) F. Podebrad, et al.: Clin. Chim. Acta 292, 93 (2000), (3) A.B. Van Kuilenburg, et al.: Biochem. J. 379, 119 (2004)

      InChi

      InChI=1S/C4H9NO2/c1-3(2-5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1

      Quantity

      100 mg, 500 mg, Bulk

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