Ordering
Available Variants5 g
CHA.26553-5g
Price
€51.90
Available – Dispatch in 14 days
25 g
CHA.26553-25g
Price
€243.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.26553-5g | €51.90 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.26553-25g | €243.20 |
≥98.0% (sum of enantiomers, GC)
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) | C9H13NO |
|---|---|
| CAS Number | 41851-59-6 |
| Molecular Weight | 151.21 |
| UNSPSC Code | 12352112 |
| NACRES | NA.22 |
| PubChem Substance ID | 57653707 |
| MDL number | MFCD00671660 |
| Beilstein/REAXYS Number | 3196456 |
| Assay | ≥98.0% (sum of enantiomers, GC) |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405 |
| Hazard Classifications | Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(S)-(−)-4-Methoxy-α-methylbenzylamine, with the CAS registry number 41851-59-6, is a chiral amine compound that exhibits significant importance in various chemical and pharmaceutical applications. Its molecular structure consists of a benzene ring substituted with a methoxy group and an α-methylbenzylamine moiety, which imparts its unique chemical and physical properties. This compound is utilized as a key intermediate in the synthesis of several biologically active molecules, including pharmaceuticals and agrochemicals. The (S)-enantiomer of 4-methoxy-α-methylbenzylamine is particularly valued for its high optical purity, which is crucial for the production of enantiomerically pure compounds. As a result, (S)-(−)-4-methoxy-α-methylbenzylamine has become a vital building block in asymmetric synthesis, enabling the creation of complex molecules with precise stereochemical control.
