N-Hydroxysuccinimide CAS NO.6066-82-6

Min.Order: 1 Gram
Payment Terms: T/T,Other

Product Details

Keywords

N-Hydroxysuccinimide
6066-82-6
98% purity

Quick Details

ProName: N-Hydroxysuccinimide
CasNo: 6066-82-6
Molecular Formula: C4H5NO3
Appearance: powder
Application: intermediate
DeliveryTime: in stock
PackAge: accroding to the need
Port: Shanghai Port
ProductionCapacity: 100 Kilogram/Day
Purity: 98% purity
Storage: Keep in dark place,Inert atmosphere,Ro...
Transportation: air，sea and courier
LimitNum: 1 Gram

Superiority

Product Name:   N-Hydroxysuccinimide
Synonyms:   N-HYDROXY-2,5-PYRROLIDINEDIONE;NHS;N-HYDROXYSUCCINIMDE;N-HYDROXYSUCCINIMIDE;N-HYDROXYSUCCINIMIDE POLYMER-BOUND;NHS N-HYDROXYSUCCINIMIDE,;NHS OR HONSU;HOSu~1-Hydroxy-2,5-pyrrolidinedione
CAS:   6066-82-6
MF:   C4H5NO3
MW:   115.09
EINECS:   228-001-3
Product Categories:   Zero-Length Crosslinker;heteroXlink;Coupling ReagentsSynthetic Reagents;Coupling;Others;APIS;Biochemistry;Condensation & Active Esterification;Coupling Reactions (Peptide Synthesis);N-Substituted Maleimides, Succinimides & Phthalimides;N-Substituted Succinimides;Peptide Synthesis;Supported Reagents;Supported Synthesis;Peptide coupling agents;Medical Intermediates;Heterocycles;Other Reagents;Miscellaneous Reagents;Synthetic Organic Chemistry
Mol File:   6066-82-6.mol

Details

N-Hydroxysuccinimide Chemical Properties

mp 95-98 °C(lit.)

storage temp. 2-8°C
Water Solubility SOLUBLE
Sensitive Hygroscopic
BRN 113913
Stability: Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides, strong bases. Protect from moisture.
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)

Safety Information

Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-26-36
WGK Germany 3

Hazard Note Irritant
HS Code 29251995

N-Hydroxysuccinimide Usage And Synthesis

Chemical Properties White to pale yellow
Usage Additive used in the carbodiimide method for improved amidations and peptide couplings.