1,3-Diaminopropane CAS 109-76-2

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1,3-Diaminopropane
1,3-Diaminopropane

Base Info:

Name: 1,3-Diaminopropane

CAS: 109-76-2

Purity: 99.5%min

MOQ: 1KG

1,3-Diaminopropane Paramete

CAS No:109-76-2
Name:1,3-Diaminopropane
EINECS:203-702-7
FormulaC3H10N2
Weight74.12
Brand NameLook Chemical
Place of OriginChina
Other Names:1,3-Propanediamine; 3-Propanediamine; Trimethylenediamine
Type:APIs; Organic chemical raw materials
Product Model:LC-109-76-2
Shelf Life3 Years
UsageFor Organic Synthesis
FormLiquid

What is 1,3-Diaminopropane?

1,3-Propylenediamine is a low-level aliphatic diamine with active chemical properties. It can be widely used in epoxy resin curing agents, chemical mechanical polishing, polyamide resins, lubricant additives, oil passivators, corrosion inhibitors and pharmaceutical intermediates. With the development of society and technology, the application scope of 1,3-propylenediamine is also expanding, and the market demand is increasing year by year. Therefore, 1,3-propylenediamine is an organic chemical intermediate with broad development prospects.

1,3-Propylenediamine is a polar compound that can form hydrogen bonds. There are unshared electron pairs on the nitrogen atom. Because this pair of unshared electron pairs is nucleophilic, the chemical properties are relatively active and it is easy to react with some electrophilic compounds. If it is an organic base, it can react with organic acids and inorganic acids to generate corresponding salts; react with alkylating agents such as halogenated hydrocarbons and alcohols to generate higher-level amines; undergo acylation reactions with organic acids, acyl chlorides, esters and anhydrides; generate alkylamines with unsaturated compounds; and undergo dehydration condensation reactions with dibasic acids upon heating to generate polyamide resins. In addition, 1,3-propylenediamine can also react with cyanides, nitriles, sulfides, epoxy compounds, phosphides, etc.

Physical Properties

Product Packaging

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1,3-Diaminopropane Uses

1,3-Propylenediamine is a low-level aliphatic diamine with active chemical properties. It can be widely used in medicine, pesticides, dyes, petrochemicals, semiconductor manufacturing and polymer industries.

  • Epoxy curing agent
    In addition to being used directly as an epoxy resin curing agent, 1,3-propylenediamine can also be made into a latent curing agent through chemical modification. The so-called latent curing agent is a curing agent that has a certain storage stability at room temperature after being combined with epoxy resin, and can quickly crosslink and cure epoxy resin under conditions such as heating, light, moisture or pressure.
  • Used in oil additives
    Oil additives refer to certain chemical substances that can significantly improve the original properties of oil products or give oil products certain new qualities when added to oil products. Propylene diamine has good oil solubility compared to ethylenediamine. Early oil passivators were prepared using ethylenediamine. Due to the crystallinity of ethylenediamine, propylenediamine (1,2-propylenediamine and 1,3-propylenediamine) is currently used as a passivator raw material in countries around the world.
  • Used in mineral processing industry
    Dodecylamine is a commonly used collector in reverse flotation process, but its effect is not very obvious in bauxite reverse flotation, and its ability to collect aluminum silicate minerals is not strong. N-dodecyl-1,3-propylenediamine is a cationic surfactant. It is mainly used for the separation of hematite from quartz and hematite from common pyroxene in flotation. It is also used for the separation of quartz from feldspar and the separation of barite from fluorite.
  • Used for the synthesis of Schiff bases and their metal complexes
    1,3-propylenediamine can be regarded as a compound corresponding to the replacement of two hydrogen atoms in the molecule by two amino groups. It can generate Schiff bases with carbonyl compounds. At the same time, because the molecule contains two highly electronegative nitrogen atoms, 1,3-propylenediamine exhibits strong coordination ability and can form stable complexes with almost all metal elements.
  • Used as pharmaceutical synthesis intermediates
    Synthesis of Amifostine
    Amifostine is a broad-spectrum cell protectant recognized by international authoritative organizations. It was developed by the American Bioscience Corporation of Texas and produced by Alza Pharmaceuticals. It was approved by the US FDA for marketing in the United States in 1996. It is usually used as a normal cell protector during radiotherapy and to prevent and reduce the cumulative nephrotoxicity, neurotoxicity and damage to the hematopoietic system caused by multiple doses of cisplatin chemotherapy for advanced ovarian cancer or non-small cell lung cancer and cyclophosphamide chemotherapy for advanced ovarian cancer. Amifostine is mainly made from 1,3-propylenediamine through condensation, bromination and salt formation.

    Synthesis of Methimidine Propylene Diamine
    Methimidine Propylene Diamine-ETDA (MPE for short) is a biological genetic material DNA cutting agent, which has extremely wide applications in the determination of drug action sites, biochemical research and cutting reagent standards, especially in the field of life sciences. Methimidine Propylene Diamine is an essential compound for the synthesis of MPE, which is mainly made from 2-aminobiphenyl as the starting material through nitration, amidation, cyclization, methylation, reduction and amidation reactions.

Applications of 1,3-Diaminopropane

1,3-propylenediamine can be used in the preparation of fluorescent sensor films that are sensitive to nitroaromatic compounds. The fluorescent sensor film uses fluorescence as the output signal. Among sensor materials, it has the advantages of high sensitivity and good selectivity. In addition, compared with liquid-phase fluorescent sensors, it also has the advantages of not polluting the system to be tested and easy to device.

Unless gasoline contains additives that effectively control deposits, deposits tend to accumulate inside the engine. 1,3-propylenediamine can be used to prepare Mannich reaction products with strong cleaning ability in the fuel, which can effectively control the engine deposits in the internal combustion engine.

1,3-propylenediamine can be used as a template to prepare porous inorganic materials of metal phosphate, which can be used in ion exchange, adsorption, catalysis and other inorganic functional materials.

1,3-propylenediamine can be used to prepare N,N′-alkylenebis(tetrabromophthalamide), which is an important type of plastic flame retardant. It has excellent flame retardant effect and low toxicity. It is used in plastic products without frost, does not affect the electrical and mechanical properties of the products, and has outstanding thermal stability and UV resistance. It is an excellent flame retardant for various engineering plastics and thermoplastics.

1,3-propylenediamine can be used to prepare amino-terminated polyoxyethylene, which has biological activity and can be combined with carboxyl, sulfhydryl or acylamino groups on proteins through its amino group to modify proteins, and give some advantages of polyoxyethylene such as amphiphilicity, non-toxicity, low immunogenicity, good biocompatibility, a wide variety, stability, and the ability to improve protein performance to the modified protein.

1,3-Propylenediamine can be used to prepare a stripper composition, which is used for stripping resist residues and metal oxide products derived from metal wiring, especially for stripping ashing residues in through holes, wherein the resist residues are left after the resist used in the process of forming semiconductor elements on semiconductor substrates such as silicon wafers is removed by ashing.

Using 1,3-propylenediamine as a raw material, compounds with good antibacterial pharmacological activity such as p-dimethylaminobenzaldehyde propylenediamine can be prepared.

1,3-Propylenediamine can be used to prepare a wood preservative composition, which has good activity against termites and fungi, and can give wood efficient antiseptic, insect-proof and termite-proof properties.

1,3-Propylenediamine can also be used as a crosslinking agent for polymers, and can be used in the chain extension and spraying of polyurethanes. It can also be used to synthesize water-soluble polyamides and used as carriers for macromolecular drugs.

In addition, 1,3-propylenediamine can be used as a corrosion inhibitor in metal protection, can also be used to prepare industrially used bactericides, can be used as a solvent and is widely used in some other organic syntheses.

Product Data

1. Certificate Of Analysis (COA)

2. Material Safety Data Sheet (MSDS)

3. Route of synthesis (ROS)

4. Method of Aanlysis (MOA)

5. Nuclear Magnetic Resonance (NMR)

6. Packing pictures and loading video before loading

7. Free Sample

8. Factory audit

1,3-Diaminopropane Manufacturer & Supplier

As an experienced 1,3-diaminopropane manufacturer and supplier, Look Chemical is committed to producing and selling high quality products.

We cooperate and trade with 6000+ factories around the world, and our high-quality products and excellent services make us enjoy a high reputation internationally.

As 1,3-diaminopropane supplier, Look Chemical provides supply chain solutions to partners and customers in a wide range of industries. We offer competitive pricing and quality products.

If you have a demand for this product, please contact our company’s sales staff, we will provide you with a solution in the shortest time.

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Loading and Transportation

1. ≤50kg, Express delivery recommended, usually called as DDU service;

2. ≤500kg, Air shipping recommended, usually called as FOB, CFR, or CIF service;

3. >500kg, sea shipping recommended, usually called as FOB, CFR, or CIF service;

4. For high value products, please select air shipping and express delivery for safe.

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Related References

  1. Zou Xiaoyan. Study on luminescence and molecular magnetism of 1,3-propylenediamine-based Salen rare earth complexes[D]. Heilongjiang University, 2013.
  2. WikiPedia