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L(+)-Ascorbic acid sodium salt, 10 mg, 10 mg

≥99 %, ROTI®Click Grade
Icon_Eisstern All products identified as being particularly temperaturesensitive are shipped in special ice boxes with freezer packs or in dry ice.
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Sodium L(+)-ascorbate
Empirical formula C6H7O6Na
Molar mass (M) 198,11 g/mol
Density (D) 1,8 g/cm³
Melting point (mp) 220 °C
Storage temp. +4 °C
Transport temp. cooled
WGK 1
CAS No. [134-03-2]
EG-Nr. 205-126-1

for Click Chemistry

Important information on refrigerated transports
Product details
Type analysis

€14.55/Pack Qty. 

excl. VAT. | 10 mg per Pack Qty.

Art. No. 7819.1

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Important information on refrigerated transports

All products identified as being particularly temperature‑sensitive are shipped in special ice boxes with freezer packs or in dry ice.
Additional costs
resulting from such, will be invoiced (further information on request).

Please note: In order to guarantee optimum product quality, the dispatch of refrigerated transport products will be carried out on Mon and Tue only outside Germany!
Slight delays in delivery are therefore possible.



L(+)-Ascorbic acid sodium salt
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General information

Vitamins

Vitamins are involved in many metabolic reactions. We can supply a range of high-purity substances suitable for biochemical applications in research and development.


Tip:

TBTA (Art.No. 7814) is suitable as copper-stabilising ligand for reactions in organic solvents. THPTA (Art.No. 7822) on the other hand is an optimal ligand for reactions in aqueous media.


Reagents for Click Chemistry

Starting from diverse copper catalyst sources, over Cu(I) stabilising ligands to buffer additives and solvents, you will find all necessary reagents in the special ROTI®Click quality to perform your click reactions here.


Click Chemistry

The copper(I)‑catalysed azide-alkyne cycloaddition (CuAAC) is the most prominent example of a group of reactions named click reactions. According to Sharpless’ definition, these reactions are characterised by high yields, mild reaction conditions, and by their tolerance of a broad range of functional groups.[1-3] Typically, the reactions require simple or no workup or purification of the product. The most important characteristic of the CuAAC reaction is its unique bioorthogonality as neither azide nor terminal alkyne functional groups are generally present in natural systems.


References:
1 H. C. Kolb, M.G. Finn, K. B. Sharpless, Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
2 C.W. Tornoe, C. Christensen, M. Meldal, J. Org. Chem. 2002, 67, 3057-3064.
3 V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708-2711; Angew. Chem. Int. Ed. 2002, 41, 2596-2599.


Certificates of Analysis

You can search for and download your certificate of analysis for the selected product here. Please provide your batch number.
The following analysis certificates have been found:

Type analysis

Appearancewhite crystals  
Assay≥99 %  

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