O-tert-Butyl-L-threonine TCI B3398

Chemical Identity

CAS No.: 4378-13-6
PubChem: CID 6951357·SID 87557830
Formula: C8H17NO3
Molecular weight: 175.23 g/mol
Purity: >98.0%(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,3R)-2-amino-3-[(2-methylpropan-2-yl)oxy]butanoic acid
SMILES: C[C@H]([C@@H](C(=O)O)N)OC(C)(C)C
InChIKey: NMJINEMBBQVPGY-RITPCOANSA-N

Rp 875.700,00

~~Rp 627.900,00~~ Rp 875.700,00

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O-tert-Butyl-L-threonine is a chemical compound widely used in catalytic reactions and organic synthesis within laboratory settings. As an organocatalyst, it plays a crucial role in accelerating chemical reactions without the need for heavy metals. This makes it a valuable tool in modern synthetic chemistry, where the use of environmentally friendly and cost-effective reagents is increasingly important. Its ability to facilitate asymmetric reactions and substitution reactions has made it a popular choice among researchers aiming to produce chiral compounds with high enantiomeric purity.

The compound is known for its stability and controlled reactivity, which are key factors in its preference for organic chemistry research. It exhibits good solubility in organic solvents, which simplifies the process of dissolution and reaction setup in the lab. Additionally, its thermal stability allows it to be used in a variety of reaction conditions, including those that require precise temperature control. These properties make it a reliable and versatile reagent for both academic and industrial research applications.

In Indonesian laboratories, O-tert-Butyl-L-threonine is commonly used in organic chemistry research, particularly in the synthesis of asymmetric compounds and organic catalysis. It is a standard material in many research institutions and universities, where it supports the development of new synthetic methodologies and the exploration of catalytic mechanisms. Its availability and effectiveness have made it an essential component in the chemical toolkit of Indonesian scientists.

TCI brochures (PDF)

Asymmetric Organocatalysts 2025-06-12 · p. 8
Asymmetric Synthesis 2026-03-18 · p. 7
Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 30

Related TCI products

Asymmetric synthesis applications benefit from O-tert-Butyl-L-threonine's ability to control stereochemistry in reaction products, making it ideal for creating chiral compounds with high enantiomeric purity.
Organic catalysis research relies on this compound due to its role in accelerating reactions without the need for metal-based catalysts, aligning with green chemistry principles.
Substitution reactions in synthetic pathways often use this material because of its reactivity and compatibility with various functional groups, enhancing reaction efficiency.
Structural modification of organic molecules is supported by its use in controlled reaction environments, allowing for precise molecular design and functional group manipulation.
Research into catalytic mechanisms benefits from its stability and predictable behavior, enabling detailed kinetic and mechanistic studies in controlled laboratory settings.

Brand	TCI
CAS number	4378-13-6
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > Organocatalysts [Catalysis]
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from moisture and direct sunlight

O-tert-Butyl-L-threonine should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in airtight containers to minimize exposure to moisture and air, which could affect its reactivity. Since it is a chemical reagent, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. While it is generally stable under normal storage conditions, it is important to avoid prolonged exposure to extreme temperatures or high humidity. Proper labeling and storage in designated chemical cabinets are essential to maintain a safe and organized laboratory environment.

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