β-Galactopyranose, TMS

• Formula: C₂₁H₅₂O₆Si₅
• Molecular weight: 541.0615
• IUPAC Standard InChI: InChI=1S/C21H52O6Si5/c1-28(2,3)22-16-17-18(24-29(4,5)6)19(25-30(7,8)9)20(26-31(10,11)12)21(23-17)27-32(13,14)15/h17-21H,16H2,1-15H3/t17-,18+,19+,20-,21+/m0/s1 Copy

  
• IUPAC Standard InChIKey: PPFHNIVPOLWPCF-XIYVOTBMSA-N Copy
• CAS Registry Number: 32166-97-5
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • α-D-Mannopyranose, 5TMS derivative
  • β-D-Glucopyranose, 5TMS derivative
  • α-D-Glactopyranose, 5TMS derivative
  • α-D-Glucopyranose, 5TMS derivative
  • α-D-Galactose, TMS
  • β-Gulopyranose, TMS
  • [2H]Mannose, TMS
  • Galactose, TMS
  • A-Psicopyranose, TMS
  • A-Sorbopyranose, TMS
  • B-Psicopyranose, TMS
  • B-Sorbopyranose, TMS
  • α-Mannose, TMS
  • α-Mannopyranose, TMS
  • D(+)-Talose, aldol, TMS
  • D-Altrose, aldol, TMS
  • α-Allopyranose, TMS
  • α-Altropyranose, TMS
  • α-Gulopyranose, TMS
  • α-Idopyranose, TMS
  • α-Talopyranose, TMS
  • β-Allopyranose, TMS
  • β-Altropyranose, TMS
  • β-Idopyranose, TMS
  • β-Mannopyranose, TMS
  • β-Talopyranose, TMS
  • D-Glucopyranose, penta-TMS
  • α-Glucopyranoside, TMS
  • Glucose, TMS # 2
  • β-D-(+)-Mannopyranose, 5TMS derivative
  • D-(+)-Galactopyranose, 5TMS derivative (isomer 1)
  • D-(+)-Galactopyranose, 5TMS derivative (isomer 2)
  • β-D-Allopyranose, 5TMS derivative
  • α-D-(+)-Talopyranose, 5TMS derivative
  • β-D-(+)-Talopyranose, 5TMS derivative
  • α-D-Allopyranose, 5TMS derivative
• Other names: β-Galactose, TMS; β-D-Galactose, TMS
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• Information on this page:
  • Gas Chromatography
  • References
  • Notes
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Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Kovats' RI, polar column, isothermal

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Normal alkane RI, non-polar column, temperature ramp

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Martinez-Castro, Paez, et al., 1989
Martinez-Castro, I.; Paez, M.I.; Sanz, J.; Garcia-Raso, A., Gas Chromatographic Behaviour of Carbohydrate Trimethylsilyl Ethers. II. Aldohexoses, J. Chromatogr., 1989, 462, 49-60, https://doi.org/10.1016/S0021-9673(00)91335-9 . [all data]

Saura-Calixto, Cañellas, et al., 1984
Saura-Calixto, F.; Cañellas, J.; García-Raso, A., Gas chromatograph analysis of surgars and sugar-alcohols in the mesocarp, endocarp, and kernel of almond fruit, J. Agric. Food Chem., 1984, 32, 5, 1018-1020, https://doi.org/10.1021/jf00125a017 . [all data]

Frank, Meuleye, et al., 2007
Frank, T.; Meuleye, B.S.; Miller, A.; Shu, A.-Y.; Engel, K.-H., Metabolite profiling of two low phytic acid (Ipa) rice nutants, J. Agric. Food Chem., 2007, 55, 26, 11011-11019, https://doi.org/10.1021/jf0723559 . [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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