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Informazioni su questo articolo
Formula condensata:
C2H5CH(OH)CO2Na
Numero CAS:
Peso molecolare:
126.09
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
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Servizio Tecnico
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Permettici di aiutartiLivello qualitativo
Saggio
97%
Stato
solid
Punto di fusione
133-135 °C (lit.)
Gruppo funzionale
hydroxyl
Stringa SMILE
[Na+].CCC(O)C([O-])=O
InChI
1S/C4H8O3.Na/c1-2-3(5)4(6)7;/h3,5H,2H2,1H3,(H,6,7);/q;+1/p-1
MOSCXNXKSOHVSQ-UHFFFAOYSA-M
Categorie correlate
1 of 4
Questo articolo | 287482 | N605 | B2912 |
|---|---|---|---|
| assay 97% | assay 97% | assay 97% | assay ≥97% |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 200 |
| form solid | form powder | form powder | form solid |
| mp 133-135 °C (lit.) | mp - | mp >300 °C (lit.) | mp - |
| functional group hydroxyl | functional group sulfonic acid | functional group - | functional group - |
Applicazioni
2-Hydroxybutyric acid sodium salt was used in gas chromatographic (GC) method for the indirect enantioresolution of 2- and 3-hydroxy fatty acids[1].
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Journal of chromatography. A, 1146(2), 225-231 (2007-02-13)
A gas chromatographic (GC) method is described for the indirect enantioresolution of 2- and 3-hydroxy fatty acids (OH-FAs). It combines the derivatization of each alkylated enantiomer and the subsequent transfer with (R)-(-)-alpha-methoxy-alpha-trifluoromethylphenylacetyl chloride [(R)-(-)-MTPA-Cl, Mosher's reagent] into a diastereomeric (S)-MTPA
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The G-Project committee was erected by the Japan Society for Gastroenterological Carcinogenesis with an aim of establishing a new classification scheme based on molecular biological characteristics that would supplement the conventional TNM classification to better predict outcome. In a literature
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