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104728-29-2

1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104728-29-2 Structure

  • Basic information

    1. Product Name: 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide
    2. Synonyms: 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide
    3. CAS NO:104728-29-2
    4. Molecular Formula: C14H29N2OP
    5. Molecular Weight: 272.366621
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104728-29-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 347.8°Cat760mmHg
    3. Flash Point: 164.2°C
    4. Appearance: /
    5. Density: 0.99g/cm3
    6. Vapor Pressure: 5.24E-05mmHg at 25°C
    7. Refractive Index: 1.489
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide(104728-29-2)
    12. EPA Substance Registry System: 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^{5}-phosphacyclopent-4- ene 2-oxide(104728-29-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104728-29-2(Hazardous Substances Data)

104728-29-2 Usage

Chemical structure

1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3-diaza-2$l^5-phosphacyclopent-4-ene 2-oxide

Type of compound

Phosphorous-containing chemical compound

Applications

a. Flame retardants
b. Lubricant additives

Effectiveness

Highly effective flame retardant, particularly in polymer materials

Flammability reduction

Helps to reduce the flammability of materials

Toxic gas release

Decreases the release of toxic gases during combustion

Additional properties

Antioxidant properties

Protection

Useful for protecting materials from oxidative degradation

Industrial applications

Wide range of industrial applications due to its unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 104728-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,2 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104728-29:
(8*1)+(7*0)+(6*4)+(5*7)+(4*2)+(3*8)+(2*2)+(1*9)=112
112 % 10 = 2
So 104728-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H29N2OP/c1-6-9-11-15-13(4)14(5)16(12-10-7-2)18(15,17)8-3/h6-12H2,1-5H3

104728-29-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibutyl-2-ethyl-4,5-dimethyl-1,3,2λ<sup>5</sup>-diazaphosphole 2-oxide

1.2 Other means of identification

Product number -
Other names 1,3,2-Diazaphosphol-4-ene,2-ethyl-2-oxo-1,3-dibutyl-4,5-dimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104728-29-2 SDS

104728-29-2Relevant articles and documents

Oxidation of 1,3,2-Diazaphospholenes

Kibardin,Gryaznova,Gryaznov,Pudovik

, p. 1415 - 1417 (2007/10/03)

1,3,2-Diazaphospholenes can be oxidized by air oxygen under mild conditions. The reactions proceed by a radical mechanism. From 2-alkyl-1,3,2-diazaphospholenes oxodiazaphospholenes were obtained. Reaction of 1,3-dibutyl-2-ethoxy-4,5-dimethyl-1,3,2-diazaphospholene with oxygen leads to formation of 3-butyl-2-butylimino-2-ethoxy-1,3,2λ5-oxazaphospholene.

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