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CAS RN: 6066-82-6 | Product Number: B0249
N-Hydroxysuccinimide [Coupling Reagent for Peptide]
Purity: >98.0%(GC)(T)
Chemical Substance Law (ENCS):
5-5911
Synonyms:
- HOSu
- NHS
Product Documents:
Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH | Shipping Information |
---|---|---|---|---|---|
25G |
¥8,000
|
20 | 27 | ≥100 | |
100G |
¥15,000
|
1 | It can be shipped from Saitama warehouse on the same day* | Contact Us |
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* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Product Number | B0249 |
Purity / Analysis Method | >98.0%(GC)(T) |
Grade | SU |
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:
Chemical Substance Law (ENCS) |
5-5911 |
Transport Information:
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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