Ordering
Available Variants1 g
CHA.33863-1g
Price
€129.60
Available – Dispatch in 14 days
10 g
CHA.33863-10g
Price
€56.64
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.33863-1g | €129.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.33863-10g | €56.64 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
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) | C12H28IN |
|---|---|
| CAS Number | 34099-97-3 |
| Molecular Weight | 313.26 |
| MDL number | MFCD32062888 |
| UNSPSC Code | 12352101 |
| NACRES | NA.23 |
Safety Information Handling visibility
| pictograms |
GHS08
GHS05
GHS07
GHS09
    GHS08,GHS05,GHS07,GHS09
|
|---|---|
| signalword | Danger |
| hcodes | H304,H314,H335,H373,H410 |
| pcodes | P260 - P280 - P301 + P310 + P331 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338 + P310 |
| Hazard Classifications | Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Skin Corr. 1B - STOT RE 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4-(Thiophen-3-yl)aniline, with the CAS registry number 834884-74-1, is an organic compound that belongs to the class of anilines. This compound is characterized by the presence of a thiophene ring attached to an aniline moiety, which imparts unique chemical and physical properties. The thiophene ring, a five-membered heterocycle containing sulfur, contributes to the compounds potential biological activity and reactivity. As a building block in organic synthesis, 4-(thiophen-3-yl)aniline can be utilized in the preparation of various pharmaceuticals, agrochemicals, and materials science applications. Its reactivity towards electrophiles and nucleophiles makes it a valuable intermediate in the synthesis of complex molecules, and its properties are being explored in various research fields, including medicinal chemistry and materials science. Further studies are needed to fully elucidate its potential uses and applications.
