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Free sample for IBEM - 4-tert-Butylbenzaldehyde CAS 939-97-9 Assay ≥96.0% (GC) High Quality – Ruifu Featured Image
  • Free sample for IBEM - 4-tert-Butylbenzaldehyde CAS 939-97-9 Assay ≥96.0% (GC) High Quality – Ruifu

Free sample for IBEM - 4-tert-Butylbenzaldehyde CAS 939-97-9 Assay ≥96.0% (GC) High Quality – Ruifu

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Free sample for IBEM - 4-tert-Butylbenzaldehyde CAS 939-97-9 Assay ≥96.0% (GC) High Quality – Ruifu Detail:

Manufacturer Supply with High Purity and Stable Quality
Chemical Name: 4-tert-Butylbenzaldehyde
CAS: 939-97-9
High Quality, Commercial Production

Chemical Name 4-tert-Butylbenzaldehyde
Synonyms TBB; 4-t-Butylbenzaldehyde; 4-(tert-Butyl)benzaldehyde; p-t-Butylbenzaldehyde; p-Tertbutyl Benzaldehyde;
CAS Number 939-97-9
CAT Number RF-PI339
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C11H14O
Molecular Weight 162.23
Boiling Point 130℃/25 mmHg
Density 0.97 g/mL at 25℃
Refractive Index n20/D 1.53
Solubility Soluble in Water
Brand Ruifu Chemical
Item Specifications
Appearance Colorless to Light Yellow Liquid
Assay / Analysis Method ≥96.0% (GC)
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Package: Bottle, Barrel, 25kg/Barrel, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture.

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4-tert-Butylbenzaldehyde (CAS 939-97-9) is an important intermediate for the synthesis of medicines, dyes, flavor and fragrance compounds. It is reported to be formed during the partial oxidation of 4-tert-butyltoluene by hydrogen peroxide in glacial acetic acid, catalyzed by bromide ions in combination with cobalt(II) acetate or cerium(III) acetate. Schiff base reaction between 4-tert-Butylaniline and 4-tert-Butylbenzaldehyde in ethanol has been carried out on-chip in the matrix assisted laser desorption ionization (MALDI) chamber, the formed imine was detected in real time. Used for preparing isoxazolyl penicillin derivatives. 4-tert-Butylbenzaldehyde is suitable for use in a kinetic study to evaluate the kinetic constants (KI) for inhibition of mushroom tyrosinase by 4-substituted benzaldehydes.

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