Boc-Sta(3R,4S)-OH

CAS 66967-01-94S)-OHChemical Synthesis

Boc-Sta(3R,4S)-OH (CAS: 66967-01-9) is a protected amino acid derivative with the molecular formula C13H25NO5 and a molecular weight of 275.34. It is a key building block in peptide synthesis and chemical biology research. Its specific stereochemistry and protected functional groups make it valuable for constructing complex peptide chains and developing novel biologically active molecules. TSS supplies this compound for research and development purposes.

IUPAC: (3R,4S)-4-(Boc-amino)-3-hydroxy-6-methylheptanoic acid
Synonyms: (3R,4S)-4-(Boc-amino)-3-hydroxy-6-methylheptanoic acid

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Boc-Sta(3R,4S)-OH (4S)-OH) — chemical structure, CAS 66967-01-9; Chemistry, fine chemical supplied by Tech Serve Solutions

Amino AcidsBiochemicals and ReagentsChemical BiologyChemical SynthesisModified Amino AcidsOthersPeptide Chemistry

01 /Applications

Peptide Synthesis

Utilised as a protected amino acid building block for the synthesis of peptides and peptidomimetics. Its defined stereochemistry is crucial for creating peptides with specific biological activities.

Chemical Biology

Serves as a reagent in chemical biology for probing biological pathways and developing novel therapeutics. It can be incorporated into molecules designed to interact with specific biological targets.

Organic Synthesis

A valuable intermediate in the synthesis of complex organic molecules. The Boc-protected amine and hydroxyl groups allow for selective functionalisation in multi-step syntheses.

Biochemical Research

Employed in biochemical studies requiring unnatural amino acids or modified peptide structures. Aids in understanding protein function and designing enzyme inhibitors.

02 /Properties

Molecular weight	275.34
Empirical formula	C13H25NO5
Assay	≥97.0% (sum of enantiomers, HPLC)
Optical activity	[α]20/D −26±2°, c = 0.5% in methanol
Storage temperature	2-8°C
Melting point	137-139 °C

03 /Safety & handling

Protective equipment	Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Water hazard class (WGK, DE)	3

Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.

04 /Identifiers & registry

CAS number

66967-01-9

Beilstein registry

3613624

05 /Quality & supply

Documentation

Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.

Supply & logistics

Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.

06 /Frequently asked questions

What is Boc-Sta(3R,4S)-OH used for?

Boc-Sta(3R,4S)-OH is primarily used as a protected amino acid building block in peptide synthesis and as a reagent in chemical biology and organic synthesis for creating complex molecules and studying biological pathways.

What are the CAS number and formula for Boc-Sta(3R,4S)-OH?

The CAS number is 66967-01-9 and the empirical formula is C13H25NO5.

What grade and purity does Tech Serve Solutions supply?

Tech Serve Solutions supplies Boc-Sta(3R,4S)-OH with an assay of ≥97.0% (sum of enantiomers, HPLC). This product is supplied for research and development purposes and TSS does not represent it as USP, BP, or EP grade.

How should Boc-Sta(3R,4S)-OH be handled and stored?

Handle with appropriate personal protective equipment, including eyeshields, gloves, and a type N95 or P1 respirator filter. Store at 2-8°C to maintain its integrity.

Is Boc-Sta(3R,4S)-OH a controlled substance?

The provided data does not indicate that Boc-Sta(3R,4S)-OH is a controlled substance. Standard laboratory safety protocols should be followed.

How is Boc-Sta(3R,4S)-OH packed, shipped, and exported?

Boc-Sta(3R,4S)-OH is carefully packed to ensure stability during transit. Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals.