O-tert-Butyl-N,N'-diisopropylisourea TCI B4178

Chemical Identity

CAS No.: 71432-55-8
PubChem: CID 11041782·SID 253660124
Formula: C11H24N2O
Molecular weight: 200.32 g/mol
Purity: >95.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl N,N'-di(propan-2-yl)carbamimidate
SMILES: CC(C)NC(=NC(C)C)OC(C)(C)C
InChIKey: FESDUDPSRMWIDL-UHFFFAOYSA-N

Rp 2.279.550,00

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O-tert-Butyl-N,N'-diisopropylisourea is a synthetic reagent widely used in laboratory settings for its role in organic synthesis. This compound is particularly valuable in reactions involving the formation of C-X (non-halogen) bonds, making it an essential tool in the field of synthetic chemistry. Its unique structure allows it to participate in various types of chemical reactions, including substitution and catalytic processes. As a reagent, it is often employed to facilitate the formation of specific molecular structures, contributing to the development of new chemical compounds.

The compound is known for its chemical stability under controlled conditions, which makes it a preferred choice for many synthetic applications. Despite its stability, it is highly reactive and sensitive to moisture and air exposure, requiring careful handling. Its reactivity is a key factor in its effectiveness for complex chemical transformations. Due to its ability to maintain chemical integrity during reactions, it is often used in processes where stability and reactivity are critical.

In Indonesian laboratories, O-tert-Butyl-N,N'-diisopropylisourea is commonly used in organic chemistry research. It plays a vital role in the development of new pharmaceutical and chemical compounds. Researchers in Indonesia rely on this reagent for its reliability and effectiveness in various synthetic processes. Its application extends to both academic and industrial research, supporting advancements in chemical synthesis and innovation.

TCI brochures (PDF)

Alkylation Reagents for Ester Synthesis 2026-04-06 · p. 2

Related TCI products

Organic synthesis reactions where C-X bond formation is required, due to its ability to facilitate the formation of specific molecular structures.
Catalytic processes that benefit from the presence of isourea groups, enhancing reaction efficiency and selectivity.
Development of new pharmaceutical compounds, as it supports the synthesis of complex organic molecules with desired properties.
Research in chemical engineering, where stable and reactive reagents are essential for industrial-scale synthesis.
Academic studies in synthetic chemistry, providing a reliable reagent for teaching and experimental research.

From the TCI brochure

Alkylation of carboxylic acid in CH2Cl2 at reflux (O-dialkylisourea method, scheme on page 2)

Brand	TCI
CAS number	71432-55-8
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > C-X(Non-Halogen) Bond Formation
Pack sizes	—
Physical form	—
Storage	Requires dry, cool, and well-ventilated conditions

O-tert-Butyl-N,N'-diisopropylisourea should be stored in a dry, cool, and well-ventilated area to prevent moisture and air exposure. It is recommended to use airtight containers made of inert materials such as glass or polyethylene to maintain its chemical stability. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. Avoid contact with moisture and ensure proper ventilation during use. Regular monitoring of storage conditions is essential to maintain the integrity of the compound. Always follow standard laboratory safety protocols when working with this reagent.

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