Ordering
Available Variants5 g
CHA.48013-5g
Price
€46.02
Available – Dispatch in 14 days
25 g
CHA.48013-25g
Price
€119.40
Available – Dispatch in 14 days
100 g
CHA.48013-100g
Price
€428.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.48013-5g | €46.02 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.48013-25g | €119.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.48013-100g | €428.00 |
90%, technical grade
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
| Linear Formula | H2N(CH2)3CH(OC2H5)2 |
|---|---|
| CAS Number | 6346-09-4 |
| Molecular Weight | 161.24 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 24890860 |
| EC Number | 228-753-2 |
| Beilstein/REAXYS Number | 1739649 |
| MDL number | MFCD00008227 |
| Assay | 90% |
| Form | liquid |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | 143.6 °F - closed cup |
| flash_point_c | 62 °C - closed cup |
| ppe | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
4-Aminobutyraldehyde diethyl acetal, with the CAS number 6346-09-4, is a chemical compound that has been utilized in various synthetic applications. This compound is characterized by its functional groups, which include an amino group and an acetal moiety, making it a versatile intermediate in organic synthesis. The presence of the diethyl acetal group protects the aldehyde functionality, allowing for selective reactions at the amino group. This protection can be removed under acidic conditions to reveal the aldehyde, which can then participate in further reactions. As such, 4-Aminobutyraldehyde diethyl acetal serves as a valuable building block in the synthesis of more complex molecules, including pharmaceuticals and other biologically active compounds, and its unique properties make it a useful tool in the field of organic chemistry. Its applications are diverse and continue to be explored in research and development.
