| Weight | 115.088 g/mol |
|---|---|
| Formula | C4H5NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
N-Hydroxysuccinimide (6066-82-6)
Score:
#2098 in Physics
,
#2613 in Biochemistry
,
#6509 in Chemistry
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- The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis (Journal of the American Chemical Society, 1964)
- Adsorbents for affinity chromatography. Use of N-hydroxysuccinimide esters of agarose (Biochemistry, 1972)
- Use of esters of N-hydroxysuccinimide in the synthesis of N-acylamino acids (Journal of Lipid Research, 1967)
- N-Hydroxysuccinimide Esters in Peptide Synthesis (Journal of the American Chemical Society, 1963)
- Conjugation of Glucose Oxidase from Aspergillus niger and Rabbit Antibodies Using NHydroxysuccinimide Ester of N(4Carboxycyclohexylmethyl)Maleimide (FEBS Journal, 1979)
- Cortical fine actin filaments in higher plant cells visualized by rhodamine-phalloidin after pretreatment with m-maleimidobenzoyl N-hydroxysuccinimide ester (Protoplasma, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(=O)N(C1=O)O
-
InChIKeyNQTADLQHYWFPDB-UHFFFAOYSA-N
- Pubchem - N-Hydroxysuccinimide
- Wikipedia - N-hydroxysuccinimide
N-Hydroxysuccinimide (NHS) is an organic compound with the formula C4H5NO3. Being slightly acidic, it is an irritant to skin, eyes and mucous membranes.
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N-Hydroxysuccinimide
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