Ordering
Available Variants25 mg
CHA.87489-25mg
Price
€62.96
Available – Dispatch in 14 days
100 mg
CHA.87489-100mg
Price
€160.00
Available – Dispatch in 14 days
500 mg
CHA.87489-500mg
Price
€600.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mg | CHA.87489-25mg | €62.96 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 mg | CHA.87489-100mg | €160.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.87489-500mg | €600.00 |
≥97.0% (HPLC)
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C8H10FNO2S · HCl |
|---|---|
| CAS Number | 30827-99-7 |
| Molecular Weight | 239.69 |
| UNSPSC Code | 12352202 |
| NACRES | NA.77 |
| PubChem Substance ID | 24278240 |
| MDL number | MFCD00132962 |
| Beilstein/REAXYS Number | 7604627 |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 |
| Hazard Classifications | Eye Dam. 1 - Skin Corr. 1A |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4-(2-Aminoethyl)benzenesulfonyl fluoride hydrochloride, with the CAS number 30827-99-7, is a chemical compound that has been utilized in various biochemical and pharmacological applications. This compound is a derivative of benzenesulfonyl fluoride and contains an aminoethyl group, which provides a reactive site for further modification or conjugation. The hydrochloride salt form of this compound enhances its solubility and stability, making it more suitable for use in aqueous solutions. As a sulfonyl fluoride, it can react with nucleophiles, such as amines or thiols, to form covalent bonds, which is useful in protein modification and cross-linking studies. The compound has been employed in the development of inhibitors and probes for various enzymes and proteins, and its reactivity and selectivity make it a valuable tool in biochemical research and drug discovery.
