Skip to product information
1 of 2

TCI

CAS 7693-46-1

4-Nitrophenyl Chloroformate TCI C1400

4-Nitrophenyl Chloroformate TCI C1400

Chemical Identity

Other names
Chloroformic Acid 4-Nitrophenyl Ester
CAS No.
7693-46-1
PubChem
CID 82129·SID 87566408
Formula
C7H4ClNO4
Molecular weight
201.56 g/mol
Purity
>98.0%(T)
Storage
0-10°C
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4-nitrophenyl) carbonochloridate
SMILES
C1=CC(=CC=C1[N+](=O)[O-])OC(=O)Cl
InChIKey
NXLNNXIXOYSCMB-UHFFFAOYSA-N
MDL
MDL00007321
Regular price Rp 2.889.600,00
Regular price Rp 2.035.950,00 Sale price Rp 2.889.600,00
Sale Sold out
Shipping calculated at checkout.
Berat
Quantity
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

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

TCI C1400 4-Nitrophenyl Chloroformate (CAS 7693-46-1) is a widely used activating reagent in peptide chemistry and bioconjugation. It converts alcohols and amines into activated 4-nitrophenyl carbonates or carbamates, in which 4-nitrophenolate serves as an excellent leaving group for subsequent nucleophilic attack. This two-step approach provides controlled access to unsymmetrical carbamates, prodrug linkers, activated PEG derivatives, and immobilised ligands without handling phosgene directly. AMI Scientific offers 25 g and 250 g packs; the reagent is moisture-sensitive and performs best when stored and handled under dry conditions.

TCI brochures (PDF)

From the TCI brochure

  • Reacts with hydroxyl-terminated polymer in pyridine, CH2Cl2 to form an activated intermediate for coupling with amine target molecules

Brand —
CAS number —
Molecular formula —
Purity —
Category —
Pack sizes —
Physical form —
Storage —

—

  • Sammet (2009). 4-Nitrophenyl Chloroformate: A Versatile Coupling Reagent. Synlett doi:10.1055/s-0029-1218291
  • El Seoud et al. (2006). Kinetics of the pH‐independent hydrolyses of 4‐nitrophenyl chloroformate and 4‐nitrophenyl heptafluorobutyrate in water‐acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity. Journal of Physical Organic Chemistry doi:10.1002/poc.1081
  • Mikulec et al. (1996). Use ofp-nitrophenyl chloroformate chemistry to immobilize protein on orthopedic biomaterials. Journal of Biomedical Materials Research doi:10.1002/(sici)1097-4636(199610)32:2<203::aid-jbm8>3.0.co;2-x

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.