Propazine

Base Information

• Chemical Name: Propazine
• CAS No.: 139-40-2
• Molecular Formula: C9H16 Cl N5
• Molecular Weight: 229.713
• Hs Code.: 29336990
• European Community (EC) Number: 205-359-9
• ICSC Number: 0697
• NSC Number: 26002
• UN Number: 3077
• UNII: UYP5U99Q5T
• DSSTox Substance ID: DTXSID3021196
• Nikkaji Number: J3.630G
• Wikidata: Q1953551
• Metabolomics Workbench ID: 52208
• ChEMBL ID: CHEMBL1333189
• Mol file: 139-40-2.mol

Synonyms:2-chloro-4,6-bis(isopropylamino)-s-triazine;Geigy 30,028;Gesamil;propazine

Chemical Property of Propazine

Chemical Property:

• Appearance/Colour: Colorless powder.
• Vapor Pressure: 9.19E-06mmHg at 25°C
• Melting Point: 212-214 ºC
• Refractive Index: 1.6110 (estimate)
• Boiling Point: 373.1 °C at 760 mmHg
• PKA: 2.28±0.10(Predicted)
• Flash Point: 179.4 °C
• PSA: 62.73000
• Density: 1.162
• LogP: 2.31160
• Storage Temp.: APPROX 4°C
• Water Solubility.: 8.6mg/L(22 oC)
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 229.1094232
• Heavy Atom Count: 15
• Complexity: 169

Purity/Quality:

99% ^*data from raw suppliers

Propazine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn;N,N,Xn,T,F
• Statements: 40-50/53-39/23/24/25-23/24/25-11
• Safety Statements: 36/37-60-61-45-24-16-7

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Herbicides, Triazine
• Canonical SMILES: CC(C)NC1=NC(=NC(=N1)Cl)NC(C)C
• Inhalation Risk: A nuisance-causing concentration of airborne particles can be reached quickly when dispersed.
• Uses: 2,4-Bis(isopropylamino)-6-chloro-1,3,5-triazine is used to control annual grasses and broad-leaved weeds in milo and sweet sorghum. Herbicide.

Technology Process of Propazine

There total 3 articles about Propazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.8%

1,3,5-trichloro-2,4,6-triazine (108-77-0) + isopropylamine (75-31-0) → propazine (139-40-2)

Guidance literature:

With sodium hydroxide; In water; toluene; at 5 - 50 ℃;

Reference yield:

2,4-dichloro-6-isopropylamino-1,3,5-triazine (3703-10-4) + isopropylamine (75-31-0) → propazine (139-40-2)

Guidance literature:

With sodium hydroxide;

DOI:10.1021/op0340715

Reference yield:

→ propazine (139-40-2)

Guidance literature:

upstream raw materials:

2,4-dichloro-6-isopropylamino-1,3,5-triazine

isopropylamine

1,3,5-trichloro-2,4,6-triazine

Downstream raw materials:

2-Anilino-4,6-di(isopropylamino)-1,3,5-triazin

2,4-diamino-1,3,5-triazine

prometon

2-methylthio-4,6-bis(isopropylamino)-s-triazine

Refernces

• 1、 -. "Cycloolefin substituted heteroaromatic ring compound and application thereof". Paragraph 0287; 0316-0320; 0322. . Retrieved 2019/03/29.
• 2、 -. "ANTIFOULING COATING FILM WITH LOW FRICTIONAL RESISTANCE WITH WATER OR SEAWATER". Paragraph 0088-0089; 0104. . Retrieved 2016/10/27.