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CHEMDOR CHEMICALS CATALOG

N1,N4-Bis-Boc-spermidine

N1,N4-Bis-Boc-spermidine • CHA.35378 • CAS 85503-20-4

≥95.0% (TLC)

Catalogued Pack Sizes Technical Data Safety Context B2B Inquiry Ready
N1,N4-Bis-Boc-spermidine molecular structure
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Available Variants
1 Variant
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250 mg
SKU
CHA.35378-250mg
Price
€185.40
Available – Dispatch in 14 days
Availability & Stock Pack SKU Price (EUR)
Available – Dispatch in 14 days
Global Network - International delivery
250 mg CHA.35378-250mg €185.40
Product Overview

≥95.0% (TLC)

SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Quick Product Snapshot
Product Type Research Chemical / Reference Material
CAS Number 85503-20-4
Packaging Multiple pack-size options available
Fulfillment International B2B Freight (Dubai Hub)
Technical Specifications Structured product data
Empirical Formula (Hill Notation) C17H35N3O4
CAS Number 85503-20-4
Molecular Weight 345.48
UNSPSC Code 12352116
NACRES NA.22
PubChem Substance ID 329764223
MDL number MFCD16875671
Beilstein/REAXYS Number 6418809
Safety Information Handling visibility
Storage Class 10 - Combustible liquids
wgk WGK 3
flash_point_f Not applicable
flash_point_c Not applicable
Technical Overview & Applications Use-case context
N1,N4-Bis-Boc-spermidine, with the CAS registry number 85503-20-4, is a synthetic organic compound that serves as a protected form of spermidine. The Boc (tert-butoxycarbonyl) groups are used to temporarily block the amine functionalities, allowing for selective chemical transformations at other sites in the molecule. This compound is a key intermediate in the synthesis of various polyamine derivatives, which have been investigated for their potential biological activities, including antiviral, antibacterial, and anticancer properties. The protection of the amine groups with Boc moieties facilitates the synthesis of complex molecules by preventing unwanted side reactions and enabling the introduction of specific functional groups at the desired positions. The deprotection of the Boc groups can be easily achieved under acidic conditions, restoring the free amine groups and enabling further functionalization or biological evaluation of the resulting compounds.

Supply Chain & Fulfillment Operations

Chemdor Chemicals L.L.C., Dubai, United Arab Emirates supports structured B2B procurement workflows for N1,N4-Bis-Boc-spermidine (CAS 85503-20-4) .

  • Supplier-managed sourcing and fulfillment workflows
  • Research-scale and bulk supply via international freight networks
  • Batch-level documentation support for technical compliance and procurement review

Supporting laboratory, research, and industrial procurement operations across international markets.

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