Tetrabutylammonium Borohydride [Reducing Reagent] TCI T0917

Chemical Identity

CAS No.: 33725-74-5
PubChem: CID 9881569·SID 87576737
Formula: C16H36BN
Molecular weight: 253.3 g/mol
Purity: >96.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

SMILES: [B-].CCCC[N+](CCCC)(CCCC)CCCC
InChIKey: SGIQRFZMJGZMNT-UHFFFAOYSA-N

Rp 1.618.050,00

~~Rp 1.146.600,00~~ Rp 1.618.050,00

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Tetrabutylammonium Borohydride (TBAH) is a chemical reagent widely used in laboratory settings for its reducing properties. It serves as an effective source of hydride ions, making it essential in organic synthesis and biochemical research. This compound is particularly valuable in glycoscience, where it facilitates the reduction of carbonyl groups and other functional groups in complex molecules. Its role in enabling electron transfer during reduction reactions makes it indispensable for the synthesis of various organic compounds.

TBAH is favored for its chemical stability and resistance to decomposition, ensuring consistent performance across different experimental conditions. It is non-toxic and free from heavy metals, enhancing its safety profile compared to other reducing agents. Additionally, its solubility in organic solvents such as ethylamine and methanol makes it versatile for use in a wide range of laboratory applications. These properties make it a reliable and efficient reagent for both academic and industrial research environments.

In Indonesian laboratories, TBAH is commonly used in chemical and biochemical research, especially in institutions focused on organic synthesis and glycoscience. Its availability and cost-effectiveness make it a preferred choice for educational and research facilities aiming to develop advanced synthetic methods. The compound's reliability and safety further support its widespread use in both teaching and research settings.

TCI brochures (PDF)

Reducing Agents 2026-04-06 · p. 6
Quaternary Ammonium Salts 2025-11-10 · p. 8
Reagents for Glyco Chemistry & Biology 5th Edition · p. 148
Boron Compounds 2025-10-07 · p. 23

Related TCI products

Glycoscience Research: TBAH is ideal for reducing carbonyl groups in glycosides, aiding in the synthesis of complex carbohydrates.
Organic Synthesis: Its hydride source enables efficient reduction reactions, making it suitable for creating diverse organic compounds.
Biochemical Studies: TBAH supports the modification of biomolecules by reducing functional groups, enhancing its utility in biochemistry.
Analytical Chemistry: Its stability and solubility make it useful in analytical processes requiring controlled reduction reactions.
Teaching Laboratories: TBAH is commonly used in educational settings to demonstrate reduction mechanisms and synthetic pathways.

Brand	TCI
CAS number	33725-74-5
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

TBAH should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to avoid exposure to moisture and air, which could affect its performance. Due to its non-toxic nature, it is generally safe to handle, but standard laboratory precautions should still be followed, such as wearing gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to prevent the accumulation of any vapors. TBAH is compatible with most standard chemical storage containers, provided they are suitable for organic solvents and maintain a controlled environment. Regular inspection of storage conditions ensures the reagent remains effective for use in laboratory applications.

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