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CAS RN: 6066-82-6 | Product Number: B0249
N-Hydroxysuccinimide [Coupling Reagent for Peptide]
Purity: >98.0%(GC)(T)
Synonyms:
- HOSu
- NHS
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
25G |
$73.00
|
20 | ≥100 |
100G |
$137.00
|
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Product Number | B0249 |
Purity / Analysis Method | >98.0%(GC)(T) |
Molecular Formula / Molecular Weight | C__4H__5NO__3 = 115.09 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Hygroscopic |
CAS RN | 6066-82-6 |
Reaxys Registry Number | 113913 |
PubChem Substance ID | 87563364 |
SDBS (AIST Spectral DB) | 5311 |
MDL Number | MFCD00005516 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(GC) | min. 98.0 % |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 98.0 to 102.0 °C |
Solubility in Dioxane | lmost transparency |
NMR | confirm to structure |
Properties (reference)
Melting Point | 100 °C |
Solubility in water | Soluble |
Solubility (soluble in) | Dioxane |
GHS
Related Laws:
Transport Information:
H.S.code* | 2928.00-000 |
Application
An Additive for Condensation Reactions
Experimental procedure: A mixture of 1 (3.8 g, 17.5 mmol) and N-hydroxysuccinimide (3.0 g, 26.2 mmol) in CH2Cl2 (100 mL) and THF (50 mL) at 0 °C is treated with EDC・HCl (5.0 g, 26.2 mmol), and the mixture is stirred at the same temperature for 12 h. The reaction is quenched with H2O, and the mixture is partitioned between AcOEt and H2O. The organic phase is washed with saturated aqueous NaCl, dried (Na2SO4), filtered, and concentrated in vacuo. The residue (2) in CH2Cl2 (100 mL) is treated with 3-amino-1-propanol (2.0 mL, 26.2 mmol) at 0 °C and stirred at room temperature for 8 h. The resulting mixture is partitioned between AcOEt and H2O. The organic phase is washed with H2O (twice), saturated aqueous NaCl, dried (Na2SO4), filtered, and concentrated in vacuo. The residue is purified by silica gel column chromatography (40% AcOEt-hexane) to afford 3 as a colorless syrup (4.0 g, 84% over two steps).
References
- Mechanistic Analysis of Muraymycin Analogues: A Guide to the Design of MraY Inhibitors
PubMed Literature
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