N-Succinimidyl Bromoacetate TCI S0852

Chemical Identity

CAS No.: 42014-51-7
PubChem: CID 3565210·SID 125308013
Formula: C6H6BrNO4
Molecular weight: 236.02 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2,5-dioxopyrrolidin-1-yl) 2-bromoacetate
SMILES: C1CC(=O)N(C1=O)OC(=O)CBr
InChIKey: NKUZQMZWTZAPSN-UHFFFAOYSA-N

Rp 3.658.200,00

~~Rp 2.573.550,00~~ Rp 3.658.200,00

Sale Sold out

Shipping calculated at checkout.

Berat 100mg

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

N-Succinimidyl Bromoacetate (N-Succinimidyl Bromoacetate) is a chemical compound widely used in biochemical and biotechnological applications. It functions as an active reagent that facilitates the connection of protein molecules or other biological entities through specific chemical reactions. In laboratory settings, this compound is essential for crosslinking, a technique that enables the precise binding of two biological molecules. Its role is critical in various research areas where molecular interactions need to be studied or modified.

The compound is known for its high reactivity, particularly towards amino groups on proteins or peptides. This reactivity makes it highly effective in conjugation reactions, allowing for the attachment of ligands or labels to target molecules. Its ability to form selective and specific bonds minimizes unwanted side reactions, ensuring greater accuracy in experimental outcomes. These properties make it a preferred choice for researchers aiming for precision in their work.

In Indonesian laboratories, N-Succinimidyl Bromoacetate is commonly used in biomedical research, protein analysis, and drug development. Its relevance extends to studies on molecular interactions and protein modification, which are fundamental to scientific research in various institutions and universities. The compound supports a wide range of experimental needs, making it an essential tool for biochemists and biotechnologists.

TCI brochures (PDF)

Cross-linkers 2026-04-14 · p. 2
Bioconjugation Reagents 2026-07-07 · p. 8
Reagents for Biological Research 2025-03-11 · p. 29

Related TCI products

Biomedical research utilizes N-Succinimidyl Bromoacetate to study molecular interactions and protein modifications, offering precise conjugation capabilities for targeted labeling.
Protein analysis benefits from this compound’s ability to selectively bind to amino groups, enabling accurate modification and detection of protein structures.
Drug development leverages its reactivity to attach functional groups to biomolecules, aiding in the creation of labeled compounds for therapeutic applications.
Crosslinking experiments rely on its high reactivity and specificity, ensuring stable and targeted connections between biological molecules.
Molecular conjugation applications benefit from its ability to form selective bonds, reducing background noise and improving the accuracy of experimental results.

Brand	TCI
CAS number	42014-51-7
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Linkers and Crosslinkers
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light

N-Succinimidyl Bromoacetate should be stored in a cool, dry place away from direct light to maintain its chemical stability and reactivity. It is recommended to use airtight containers to prevent moisture exposure, which could affect its performance. Due to its reactive nature, it should be handled in a well-ventilated area and with appropriate personal protective equipment. Avoid contact with incompatible substances to ensure safety. Proper labeling and storage conditions are essential to maintain the compound’s effectiveness and ensure safe handling in laboratory environments.

—