REZULTATŲ PUSLAPIS

Polysaccharide / carbohydrate polyol material

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Rezultato Nr.: 20260114194206029143201 Savininkas: publicuser Komentarai: 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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Top15

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Top 15 candidates

Reference library candidates

Rank Match % Compound Name Formula / SMILES Library preview Action
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Based on the library matches and evidence above.

Conclusion

Polysaccharide / carbohydrate polyol material

General assessment
Bendras pasitikėjimas
#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

Bibliotekos pagrindinis atitikmuo
(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 Literatūra pagrįstas priskyrimas Juosta ties 1024 cm-1 priskiriama C–O stretching in polysaccharide ring[5]. [5] LLM patikimumas
2 875 0.40 Literatūra pagrįstas priskyrimas Juosta ties 875 cm-1 priskiriama carbohydrate[1]. [1] LLM patikimumas
3 1159 0.33 Literatūra pagrįstas priskyrimas Juosta ties 1159 cm-1 priskiriama asymmetric C–O–C stretching (glycosidic bridge)[5]. [5] LLM patikimumas
4 1424 0.29 Literatūra pagrįstas priskyrimas Juosta ties 1424 cm-1 priskiriama CH₂ bending (C6 scissoring)[5][6]. [5], [6] LLM patikimumas
5 · 3291 0.27 - - - -
6 1316 0.25 Literatūra pagrįstas priskyrimas Juosta ties 1316 cm-1 priskiriama CH₂ wagging[5]. [5] LLM patikimumas
7 2918 0.18 Literatūra pagrįstas priskyrimas Juosta ties 2918 cm-1 priskiriama alkyl C-H vibration[7]. [7] Bendras pasitikėjimas
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
Diskusija

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