1-Benzyl-3-p-tolyltriazene [for Esterification] TCI B0949

Chemical Identity

CAS No.: 17683-09-9
PubChem: CID 87234·SID 87563910
Formula: C14H15N3
Molecular weight: 225.29 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-(benzyldiazenyl)-4-methylaniline
SMILES: CC1=CC=C(C=C1)NN=NCC2=CC=CC=C2
InChIKey: IWCGEJKKDAJKJE-UHFFFAOYSA-N

Rp 1.246.350,00

~~Rp 871.500,00~~ Rp 1.246.350,00

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TCI B0949 1-Benzyl-3-p-tolyltriazene is a chemical compound widely used in organic synthesis as a building block for complex molecule construction. This compound is specifically designed for esterification reactions with various carboxylic acids, making it a valuable tool in synthetic chemistry. Its triazene structure allows for versatile chemical reactivity, enabling chemists to create a wide range of derivatives. In the laboratory, it plays a crucial role in the development of new compounds and molecular modifications, supporting both academic and industrial research efforts.

The compound is known for its chemical stability under controlled conditions, although it is highly sensitive to moisture and air exposure. These properties make it a preferred choice for researchers seeking precision in their synthetic processes. Its ability to participate in multiple chemical reactions enhances its utility in diverse experimental setups. The compound’s reactivity and structural versatility make it an essential component in advanced chemical research, particularly in the field of organic synthesis.

In Indonesian laboratories, TCI B0949 1-Benzyl-3-p-tolyltriazene is commonly used in organic chemistry research, especially in the synthesis of new compounds and molecular modifications. Researchers from educational institutions and research organizations frequently utilize this compound for experiments requiring high reactivity and precise structural control. Its role in supporting innovation and discovery in chemical research is well recognized in the scientific community.

Advantages (TCI brochure)

Member of the 1-alkyl-3-p-tolyltriazenes that react rapidly with carboxylic acids under mild conditions to give esters in high yields

TCI brochures (PDF)

GC Derivatization Reagents 2026-03-25 · p. 4
Alkylation Reagents for Ester Synthesis 2026-04-06 · p. 5

Related TCI products

Organic Synthesis: This compound is ideal for esterification reactions, enabling the creation of complex organic molecules with high reactivity.
Molecular Modification: Its versatile structure allows for the synthesis of various derivatives, supporting research in compound development.
Academic Research: Used in university laboratories for teaching and experimental purposes, it aids in understanding chemical reactivity and synthesis techniques.
Industrial Chemistry: Applied in the production of specialty chemicals, it supports the development of new materials and pharmaceuticals.
Analytical Chemistry: Its chemical properties make it useful for testing and validating synthetic pathways in laboratory settings.

From the TCI brochure

Esterification of carboxylic acids; alkylation of phenols, imides and enolized ketones (as stated for the 1-alkyl-3-p-tolyltriazene group)

Brand	TCI
CAS number	17683-09-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a dry, cool, and well-ventilated area away from moisture and air exposure

This compound should be stored in a dry, cool, and well-ventilated area to prevent moisture and air exposure, which can affect its stability. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its integrity. Due to its sensitivity, it should be handled in a controlled environment with appropriate personal protective equipment. Avoid contact with moisture and ensure that storage conditions are consistent to preserve its chemical properties. Regular monitoring of storage conditions is advised to maintain the compound’s effectiveness in laboratory applications.

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