N,N-Dimethylformamide Di-tert-butyl Acetal [for Esterification] TCI D1303

Chemical Identity

Other names: 1,1-Di-tert-butoxytrimethylamine · N,N-DMF Di-tert-butyl Acetal
CAS No.: 36805-97-7
PubChem: CID 547712·SID 87567826
Formula: C11H25NO2
Molecular weight: 203.33 g/mol
Purity: >98.0%(N)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N,N-dimethyl-1,1-bis[(2-methylpropan-2-yl)oxy]methanamine
SMILES: CC(C)(C)OC(N(C)C)OC(C)(C)C
InChIKey: DBNQIOANXZVWIP-UHFFFAOYSA-N
MDL: MDL00015002

Rp 3.895.500,00

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Volume 5mL 25mL

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Dokumen Keamanan & Mutu

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N,N-Dimethylformamide Di-tert-butyl Acetal is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key building block in organic synthesis, it enables the formation of esters through efficient and controlled chemical processes. This compound is particularly valued for its ability to react with various carboxylic acids, making it a versatile reagent in synthetic chemistry. Its stability and reactivity make it a reliable choice for researchers working on complex molecular structures.

The compound's chemical properties, including its stability and reactivity, make it a preferred choice for laboratory applications. It is known for its ability to undergo esterification efficiently, which is crucial in the synthesis of ester compounds with diverse industrial and pharmaceutical applications. Its non-heterocyclic nature allows it to be used in a wide range of chemical reactions without interfering with other functional groups. This makes it a go-to material for chemists seeking reliable and consistent results.

In Indonesian laboratories, N,N-Dimethylformamide Di-tert-butyl Acetal is commonly used in organic chemistry research. It is a staple in both academic and industrial settings, where its reliability and efficiency are highly appreciated. Its availability in liquid form and ease of use further contribute to its popularity among researchers. Its non-volatile nature also ensures safety during handling and storage, making it a trusted reagent in controlled laboratory environments.

Advantages (TCI brochure)

Liquid at room temperature and easy to handle
Stable at room temperature when stored away from moisture

TCI brochures (PDF)

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

Related TCI products

Organic synthesis for esterification reactions due to its efficient and stable chemical properties.
Pharmaceutical research for the development of ester-based compounds with therapeutic applications.
Industrial chemistry applications where ester compounds are required for product formulation.
Academic research in chemical laboratories for teaching and experimental purposes.
Polymer science for the synthesis of ester-functionalized polymers with specific properties.

From the TCI brochure

Esterification reagent for fatty acids giving alkyl esters
Conversion of amino acids into N-dimethylaminomethylene-O-alkyl esters in one step

Brand	TCI
CAS number	36805-97-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry place away from direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. While it is relatively stable under normal storage conditions, it should not be exposed to extreme temperatures or incompatible substances. Proper labeling and safe storage practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.

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