TUDALEN CANLYNOL

Polysaccharide / carbohydrate polyol material

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Rhif Canlyniad: 20260114194206029143201 Perchennog: publicuser Sylwadau: 0
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FTIR ANALYSIS REPORT

FTIR Spectrum Analysis Report

No.: 20260114194206029143201 Date: Reported by: FTIR.fun Contact: [email protected]

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Conclusion

Polysaccharide / carbohydrate polyol material

General assessment
Hyder cyffredinol
#2057 Current rank 1
Conclusion
  1. Library Top‑1 match (trisaccharide, similarity 0.918) strongly aligns with the observed carbohydrate pattern.
  2. The band at 1024 cm⁻¹ is attributed to C–O ring stretching typical of polysaccharides.
  3. The peak at 1159 cm⁻¹ arises from the asymmetric C–O–C glycosidic bridge, a hallmark of carbohydrate polymers.
Evidence & interpretation
Evidence

Key evidence

Cyfatebiaeth arweiniol llyfrgell
(2R,3R,4S,5S,6R)-2-[(2S,3S,5R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol #2057
Limitations

Evidence that limits the conclusion

  • Direct literature assignments attribute the 1024 cm⁻¹ band to phosphate [2], the 1159 cm⁻¹ band to aromatic [7], and the 1424 cm⁻¹ band to N–H [3], which are not conventional for pure sugars; however, the overall pattern argues against a dominant phosphate or aromatic component.
  • The 875 cm⁻¹ band is reported as carbonate [5], which is not typical for simple carbohydrates.
  • Although the polysaccharide fingerprint is clear, the conflicting peak assignments suggest the presence of minor contaminants (e.g., protein, phosphate, or inorganic carbonate) or that some bands have been misinterpreted; the exact molecular identity beyond a polyol class cannot be firmly established from FTIR alone.
  • The library‑retrieved trisaccharide is one possible match, but the presence of amide/amine and phosphate markers makes it uncertain.
Recommendation

Suggested next verification

  • Complementary techniques such as NMR, mass spectrometry, or phosphate/protein assays are recommended to resolve the composition.
  • If the sample is of biological origin, enzymatic digestion or specific staining could clarify the presence of non‑carbohydrate components.
Peak analysis

Detected peaks and interpretation

★ = Literature-supported peak assignment.

Index Characteristic Wavenumber Absorbance Evidence One-line interpretation Citation Confidence
1 1024 1.00 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 1024 cm-1 wedi'i neilltuo i C–O stretching in polysaccharide ring[5]. [5] Hyder LLM
2 875 0.40 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 875 cm-1 wedi'i neilltuo i carbohydrate[1]. [1] Hyder LLM
3 1159 0.33 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 1159 cm-1 wedi'i neilltuo i asymmetric C–O–C stretching (glycosidic bridge)[5]. [5] Hyder LLM
4 1424 0.29 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 1424 cm-1 wedi'i neilltuo i CH₂ bending (C6 scissoring)[5][6]. [5], [6] Hyder LLM
5 · 3291 0.27 - - - -
6 1316 0.25 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 1316 cm-1 wedi'i neilltuo i CH₂ wagging[5]. [5] Hyder LLM
7 2918 0.18 Aseiniad a gefnogir gan lenyddiaeth Mae'r band yn 2918 cm-1 wedi'i neilltuo i alkyl C-H vibration[7]. [7] Hyder cyffredinol
Literature

References

Appendix

Sample information and raw spectrum

Original uploaded spectrum for reference and verification.

Baseline correction method: Asymmetric Least Squares Smoothing

The wavelength range for analysis(cm-1): N/A

Raw spectrum without baseline correction or other processing:

Sample spectrum image
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