| SpectraBase Compound ID | AVWEMtAwwEC |
|---|---|
| InChI | InChI=1S/C28H44N2O23.Na/c1-5(33)29-9-18(11(35)7(3-31)47-25(9)46)49-28-17(41)15(39)20(22(53-28)24(44)45)51-26-10(30-6(2)34)19(12(36)8(4-32)48-26)50-27-16(40)13(37)14(38)21(52-27)23(42)43;/h7-22,25-28,31-32,35-41,46H,3-4H2,1-2H3,(H,29,33)(H,30,34)(H,42,43)(H,44,45);/q;+1/p-1/t7-,8-,9-,10-,11-,12-,13+,14+,15-,16-,17-,18-,19-,20+,21+,22+,25-,26+,27-,28-;/m1./s1 |
| InChIKey | YWIVKILSMZOHHF-QJZPQSOGSA-M |
| Mol Weight | 798.6 g/mol |
| Molecular Formula | C28H43N2NaO23 |
| Exact Mass | 798.21543 g/mol |
Transmission Infrared (IR) Spectrum
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| SpectraBase Spectrum ID | 3XLn9ZjUO30 |
|---|---|
| Name | Sodium hyaluronate |
| Source of Sample | Acros Organics |
| Catalog Number | 251770010 |
| Lot Number | A0375841 |
| Accessory | TRANS *14560FA0 |
| Acquisition Mode | double sided, forward-backward |
| Actual Signal Gain | 2 |
| Actual Signal Gain 2nd Channel | 1 |
| Additional Data Treatment | 0 |
| Analog Signal 1 | 0.270603 |
| Analog Signal 2 | 0 |
| Aperture Setting | 6 mm |
| Apodization Function | Norton-Beer, medium |
| Background Measurement Channel | Sample Compartment |
| Background Peak Amplitude 2nd Channel | 1 |
| Background Peak Location 2nd Channel | 1 |
| Background Scans | 32 |
| Background Scans or Time | Scans |
| Backward Peak Amplitude | -11052 |
| Backward Peak Location | 14449 |
| Beam Splitter Setting | KBr |
| CAS Registry Number | 9067-32-7 |
| Color Properties | White to cream |
| Container ID | C-008604 |
| Copyright | Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved. |
| Data Point Format | 1 |
| Delay Before Measurement | 0 s |
| Detector Setting | RT-DLaTGS [Internal] |
| End Frequency Limit for File | 340 |
| External Synchronization | Off |
| Focal Length | 100 |
| Formula | C28H43N2NaO23 |
| Frequency of First Point | 3999.54 cm⁻¹ |
| Frequency of Last Point | 339.945 cm⁻¹ |
| High Folding Limit | 15800.5 |
| High Frequency Limit | 8000 cm⁻¹ |
| High Pass Filter | 0 |
| InChI | InChI=1S/C28H44N2O23.Na/c1-5(33)29-9-18(11(35)7(3-31)47-25(9)46)49-28-17(41)15(39)20(22(53-28)24(44)45)51-26-10(30-6(2)34)19(12(36)8(4-32)48-26)50-27-16(40)13(37)14(38)21(52-27)23(42)43;/h7-22,25-28,31-32,35-41,46H,3-4H2,1-2H3,(H,29,33)(H,30,34)(H,42,43)(H,44,45);/q;+1/p-1/t7-,8-,9-,10-,11-,12-,13+,14+,15-,16-,17-,18-,19-,20+,21+,22+,25-,26+,27-,28-;/m1./s1 |
| InChIKey | YWIVKILSMZOHHF-QJZPQSOGSA-M |
| Instrument Name | Bruker Tensor 27 FT-IR |
| Laser Wavenumber | 15800.5 cm⁻¹ |
| Low Folding Limit | 0 |
| Low Frequency Limit | 0 |
| Low Pass Filter | 10 |
| Molecular Weight | 798.633 g/mol |
| Non Linearity Correction | 0 |
| Number of Points | 15180 |
| Number of Sample Scans | 32 |
| Optical Filter Setting | Open |
| Peak Amplitude | -10566 |
| Peak Amplitude 2nd Channel | 1 |
| Peak Location | 14507 |
| Peak Location 2nd Channel | 1 |
| Phase Correction Mode | Mertz |
| Phase Resolution | 4 |
| Preamplifier Gain Background | 0 |
| Purity | 95% |
| Relative Humidity Interferometer | 20 % |
| Resolution | 2 |
| SKU | 251770010-1GR |
| SMILES | [Na+].O[C@@]1([C@](O[C@@](O[C@@]2([C@](O[C@@](O[C@]3([C@@]([C@](O[C@]([C@@]3(NC(C)=O)[H])(O)[H])(CO)[H])(O)[H])[H])([C@@]([C@]2(O)[H])(O)[H])[H])(C([O-])=O)[H])[H])([C@@]([C@]1(O[C@@]1(O[C@@]([C@@](O)([C@](O)([C@]1(O)[H])[H])[H])(C(O)=O)[H])[H])[H])(NC(C)=O)[H])[H])(CO)[H])[H] |
| Sample Spacing Divisor | 1 |
| Sample Spacing Multiplicator | 1 |
| Scan Time | 50.035 s |
| Scanner Temperature | 29.9 °C |
| Scanner Velocity | 10 kHz |
| Signal Gain, Background | automatic |
| Source of Spectrum | Bio-Rad Laboratories, Inc. |
| Start Frequency Limit for File | 4000 cm⁻¹ |
| Synonyms | Poly(β-glucuronic acid-[1→3]-β-N-acetylglucosamine-[1→4]); Hyaluronic acid sodium salt |
| Technique | KBr0 |
| Zero Filling Factor | 8 |