Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
4-Methylbenzylamine, 98%, Thermo Scientific Chemicals
CAS: 104-84-7 | C8H11N | 121.183 g/mol
| Catalog Number | Quantity |
|---|---|
| ALFA13768.14 | 25 g |
Catalog number ALFA13768.14
View Price:Sign InSign in to see your account pricing. Need an account? Register with us today.
Quantity:
25 g
Chemical Identifiers
CAS60481-36-9
IUPAC Name(3,5-dimethylphenyl)hydrazine hydrochloride
Molecular FormulaC8H13ClN2
InChI KeyRSBQANBNDXZFIY-UHFFFAOYSA-N
SMILESCl.CC1=CC(NN)=CC(C)=C1
View more
Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream to pale brown
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
FormPowder or lumps
The reactions of 1-hexanol with benzylamine and with 4-methylbenzylamine led to the corresponding imines in moderate yields. 4-methylbenzylamine in ethanol/water solution (1:4) as simultaneously absorbing and buffering background electrolyte with detection at 210 nm was found suitable for determination of the individual compounds in determination by capillary zone electrophoresis with indirect detection. Synthesis of benzimidazoles uses 4-methylbenzylamine (R 1 =4-MeBn) and 4-chlorophenyl isothiocyanate (R 2 =4-ClPh) as building blocks.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
The reactions of 1-hexanol with benzylamine and with 4-methylbenzylamine led to the corresponding imines in moderate yields. 4-methylbenzylamine in ethanol/water solution (1:4) as simultaneously absorbing and buffering background electrolyte with detection at 210 nm was found suitable for determination of the individual compounds in determination by capillary zone electrophoresis with indirect detection. Synthesis of benzimidazoles uses 4-methylbenzylamine (R 1 =4-MeBn) and 4-chlorophenyl isothiocyanate (R 2 =4-ClPh) as building blocks.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
The reactions of 1-hexanol with benzylamine and with 4-methylbenzylamine led to the corresponding imines in moderate yields. 4-methylbenzylamine in ethanol/water solution (1:4) as simultaneously absorbing and buffering background electrolyte with detection at 210 nm was found suitable for determination of the individual compounds in determination by capillary zone electrophoresis with indirect detection. Synthesis of benzimidazoles uses 4-methylbenzylamine (R 1 =4-MeBn) and 4-chlorophenyl isothiocyanate (R 2 =4-ClPh) as building blocks.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
General References:
- Viktor Krchňák,; Jennifer Smith,; Josef Vágner. A solid phase traceless synthesis of 2-arylaminobenzimidazoles. Tetrahedron Letters. 2001, 42 (9), 1627-1630.
- Nad’a Reichová,; Jiří Pazourek,; Pavla Polášková andJosef Havel. Electrophoretic behavior of adamantane derivatives possessing antiviral activity and their determination by capillary zone electrophoresis with indirect detection. Electrophoresis. 2002, 23 (2), 259-262.