• 3-Allyloxy-1,2-propanediol (CAS 123-34-2) - TCI G0189 - AMI Scientific
1 1

TCI

CAS 123-34-2

3-Allyloxy-1,2-propanediol TCI G0189

3-Allyloxy-1,2-propanediol TCI G0189
Rp 562.800,00
Rp 562.800,00
Sale Sold out
Shipping calculated at checkout.
Berat
Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 4-5 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

3-Allyloxy-1,2-propanediol, referred to in much of the literature as glyceryl allyl ether, is a bifunctional organic compound designed to serve as a starting point for building polymer chains. Its molecular structure combines one unsaturated allyl group at one end with two adjacent hydroxyl groups on a propanediol backbone at the other end. This combination places it squarely within the category of monomers and macromolecular reagents, because a single molecule already carries two distinct types of reactive site that can be addressed separately or in sequence within one laboratory synthesis route.

The characteristic that makes this material a frequent choice is its orthogonal reactivity. The allyl group is open to radical addition, thiol-ene coupling, hydrosilylation and epoxidation, while the pair of hydroxyl groups is ready to enter esterification, etherification, acetal formation and addition with isocyanates along polyurethane routes. That diol character also gives the molecule an affinity for polar solvents, so handling it in aqueous or alcoholic systems is comparatively straightforward. Researchers can employ it as a functionality-donating comonomer or as a linking unit between segments that would otherwise be difficult to join.

In Indonesian laboratories, this reagent is typically encountered in university polymer chemistry groups, materials research centres and industrial development units working on coatings, adhesives and specialty resins. It supports bench-scale exploratory synthesis as well as the preparation of modified surfaces and crosslinked networks. Because it is supplied by TCI in standard laboratory packaging, it fits readily into routine research workflows where reproducible reagent quality across repeated experiments is required.

  • Polymer synthesis as a functional comonomer, where the allyl group participates in chain growth while the two hydroxyl groups remain available for later modification of the finished polymer.
  • Polyurethane and polyester preparation, in which the vicinal diol reacts with isocyanates or acid derivatives to build chains that still carry a pendant unsaturated allyl handle.
  • Thiol-ene click chemistry studies, because the terminal allyl group undergoes efficient radical-mediated addition with thiols under mild conditions suited to bench-scale work.
  • Surface modification and grafting work, where hydrosilylation of the allyl group anchors the molecule to a substrate and leaves hydroxyl functionality exposed at the interface.
  • Crosslinker and network-former development, since a single molecule offers reactive sites of two different chemistries that can be engaged sequentially to build controlled three-dimensional architectures.

Brand TCI
CAS number 123-34-2
Molecular formula —
Purity —
Category Materials Science > Polymer/Macromolecule Reagents > Monomers
Pack sizes available in standard TCI laboratory research pack sizes; please confirm the size required when ordering.
Physical form —
Storage store according to the conditions stated on the manufacturer's label and safety data sheet.
  • Product code: G0189

Store this reagent in a cool, dry and well-ventilated area, kept tightly closed in its original supplier container and away from direct sunlight, heat sources and ignition sources. Because the compound carries an unsaturated allyl group, prolonged exposure to air, light or elevated temperature should be avoided. Use chemically compatible containers and transfer equipment, and keep the container sealed when not in use to limit moisture uptake by the hydroxyl-bearing portion of the molecule. All handling should take place in a fume hood with appropriate personal protective equipment, including safety goggles, chemical-resistant gloves and a laboratory coat. Consult the manufacturer's safety data sheet before use, and follow local institutional procedures for waste collection and disposal.

—

Produk Terkait