Sodium ascorbate

• CAS: 134-03-2
• Catalog Number: ACM134032
• Category: Other Products
• Molecular Weight: 198.11
• Molecular Formula: C6H7NaO6
• Synonyms: L-Ascorbic acid, monosodium salt
• IUPAC Name: sodium;(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate
• SMILES: C([C@@H]([C@@H]1C(=C(C(=O)O1)O)[O-])O)O.[Na+]
• InChI: PPASLZSBLFJQEF-RXSVEWSESA-M
• InChI Key: InChI=1S/C6H8O6.Na/c7-1-2(8)5-3(9)4(10)6(11)12-5;/h2,5,7-10H,1H2;/q;+1/p-1/t2-,5+;/m0./s1
• Melting Point: 220 °C
• Density: 1.66g/ml
• Appearance: powder
• Active Content: 95%
• pH: 7-8
• Physical State: Solid
• Safety Description: 24/25

Synthetic Use

Downstream Synthesis Route 1

• 134-03-2

• 15667-21-7

Reference: [1] Organic Process Research and Development, 2002, vol. 6, # 1, p. 49 - 53
[2] Tetrahedron Letters, 1992, vol. 33, # 7, p. 857 - 860

Downstream Synthesis Route 2

• 134-03-2
• 17465-86-0

• 129499-78-1

Reference: [1] Journal of Molecular Catalysis B: Enzymatic, 2013, vol. 92, p. 19 - 23

Downstream Synthesis Route 3

• 134-03-2
• 10016-20-3

• 129499-78-1

Reference: [1] Journal of Molecular Catalysis B: Enzymatic, 2013, vol. 92, p. 19 - 23

Downstream Synthesis Route 4

• 134-03-2

• 129499-78-1

Reference: [1]Chemical and Pharmaceutical Bulletin,1990,vol. 38,p. 3020 - 3023

Downstream Synthesis Route 5

• 134-03-2

• 15667-21-7

Reference: [1]Organic Process Research and Development,2002,vol. 6,p. 49 - 53
[2]Tetrahedron Letters,1992,vol. 33,p. 857 - 860

* For details of the synthesis route, please refer to the original source to ensure accuracy.