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A4715712

N-Hydroxysuccinimide , 98% , 6066-82-6

Synonym(s):
1-Hydroxy-2,5-pyrrolidinedione;HOSu;NHS;N-Hydroxysuccinimide;N-Hydroxysuccinimide, NHS

CAS NO.:6066-82-6

Empirical Formula: C4H5NO3

Molecular Weight: 115.09

MDL number: MFCD00005516

EINECS: 228-001-3

Pack Size Price Stock Quantity
5g RMB23.20 In Stock
25G RMB27.20 In Stock
100G RMB64.00 In Stock
500G RMB226.40 In Stock
2.5KG RMB986.40 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 95-98 °C(lit.)
Boiling point: 215.33°C (rough estimate)
Density  1.4769 (rough estimate)
vapor pressure  0Pa at 25℃
refractive index  1.4080 (estimate)
storage temp.  Store at +2°C to +8°C.
solubility  DMSO (Soluble), Methanol (Slightly)
pka 7.81±0.20(Predicted)
form  Liquid or Solid
color  Clear yellow-brown to brown
PH 5-7 (50g/l, H2O, 20℃)
Water Solubility  SOLUBLE
Sensitive  Hygroscopic
BRN  113913
Stability: Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides, strong bases. Protect from moisture.
InChIKey NQTADLQHYWFPDB-UHFFFAOYSA-N
LogP -2.01
CAS DataBase Reference 6066-82-6(CAS DataBase Reference)
NIST Chemistry Reference N-hydroxylsuccinimide(6066-82-6)
EPA Substance Registry System 2,5-Pyrrolidinedione, 1-hydroxy- (6066-82-6)

Description and Uses

N-hydroxysuccinimide is a synthetic ingredient used in cosmetics as an ester to soften and condition skin. It's also a reagent, a substance used to trigger a reaction that leads to a new substance, such as peptides and polymers.
N-Hydroxysuccinimide is used in cosmetics and beauty products as an ester often seen in eye creams. N-hydroxysuccinimide activates the elimination of blood originated pigments responsible for dark color and inflammation that causes under eye circles. "Infra-orbital shadows are due to the accumulation of hemoglobin and its coloured degradation products - biliverdin, bilirubin and iron - in the dermis and epidermis ... N-hydroxysuccinimide renders the iron soluble for natural elimination" (source).

N-hydroxysuccinimide (NHS) is often used to assist carbodiimide-mediated peptide coupling by forming an active ester intermediate via condensation of the surface carboxyl group and NHS. The NHS-reactive ester intermediate is susceptible to nucleophilic attack by primary amines and results in the formation of stable amide bonds between the biomaterial surface and the N-terminus of the peptide.

Safety

Symbol(GHS) 
GHS05
Signal word  Danger
Hazard statements  H315-H318
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P362+P364
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-26-36
WGK Germany  3
Hazard Note  Irritant
TSCA  Yes
HS Code  29251995

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