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99-98-9

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99-98-9 Usage

Chemical Properties

grey to black solid

Uses

Different sources of media describe the Uses of 99-98-9 differently. You can refer to the following data:
1. Base for production of methylene blue, photodeveloper, reagent for detection of hydrogen sulfide, reagent for cellulose, organic synthesis, reagent for certain bacteria.
2. N,N-Dimethyl-p-phenylenediamine is a redox indicator. Readily forms stable, red radical cation, involved in a variety of redox reactions.
3. N,N-Dimethyl-p-phenylenediamine may be used for the preparation of molecular compounds with tetracyano-p-quinodimethane (TCNQ). Polarized absorption spectra of these molecular compounds were investigated.

Synthesis Reference(s)

Chemistry Letters, 9, p. 439, 1980Tetrahedron Letters, 34, p. 2441, 1993 DOI: 10.1016/S0040-4039(00)60436-7

General Description

Colorless to reddish-violet solid. Used in the production of methylene blue and photographic developer. Used as a chemical intermediate for dyes and diazonium chloride salts and as an analytical reagent to detect chloroamine in water.

Reactivity Profile

N,N-Dimethyl-1,4-phenylenediamine neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. Incompatible with strong oxidizers, strong acids and acid anhydrides. Also incompatible with alkalis .

Hazard

Toxic by ingestion or inhalation of vapor.

Health Hazard

Lowest toxic dose with skin effect is 14 mg/kg. Irritant to skin and eyes.

Fire Hazard

When heated to decomposition, N,N-Dimethyl-1,4-phenylenediamine emits toxic fumes of nitrogen oxides.

Check Digit Verification of cas no

The CAS Registry Mumber 99-98-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99-98:
(4*9)+(3*9)+(2*9)+(1*8)=89
89 % 10 = 9
So 99-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-9-7-3-5-8(10-2)6-4-7/h3-6,9-10H,1-2H3

99-98-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A15962)  N,N-Dimethyl-p-phenylenediamine, 96%   

  • 99-98-9

  • 50g

  • 464.0CNY

  • Detail
  • Alfa Aesar

  • (A15962)  N,N-Dimethyl-p-phenylenediamine, 96%   

  • 99-98-9

  • 250g

  • 1964.0CNY

  • Detail
  • Alfa Aesar

  • (A15962)  N,N-Dimethyl-p-phenylenediamine, 96%   

  • 99-98-9

  • 1000g

  • 3992.0CNY

  • Detail
  • Sigma-Aldrich

  • (07750)  N,N-Dimethyl-p-phenylenediamine  for spectrophotometric det. of SO42-, S2-, ≥97.0%

  • 99-98-9

  • 07750-25G

  • 589.68CNY

  • Detail
  • Sigma-Aldrich

  • (07750)  N,N-Dimethyl-p-phenylenediamine  for spectrophotometric det. of SO42-, S2-, ≥97.0%

  • 99-98-9

  • 07750-100G

  • 1,745.64CNY

  • Detail
  • Aldrich

  • (193992)  N,N-Dimethyl-p-phenylenediamine  97%

  • 99-98-9

  • 193992-5G

  • 552.24CNY

  • Detail
  • Aldrich

  • (193992)  N,N-Dimethyl-p-phenylenediamine  97%

  • 99-98-9

  • 193992-100G

  • 1,736.28CNY

  • Detail
  • Aldrich

  • (193992)  N,N-Dimethyl-p-phenylenediamine  97%

  • 99-98-9

  • 193992-500G

  • 5,961.15CNY

  • Detail

99-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1,4-phenylenediamine

1.2 Other means of identification

Product number -
Other names 4-N,4-N-dimethylbenzene-1,4-diamine

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:99-98-9 SDS

99-98-9Relevant articles and documents

-

Livingston,Pariser

, p. 2944,2948,2949 (1956)

-

Developments in Dynamic Covalent Chemistries from the Reaction of Thiols with Hexahydrotriazines

Wojtecki, Rudy J.,Jones, Gavin O.,Yuen, Alexander Y.,Chin, Willy,Boday, Dylan J.,Nelson, Alshakim,García, Jeannette M.,Yang, Yi Yan,Hedrick, James L.

, p. 14248 - 14251 (2015)

Dynamic covalent chemistries have garnered significant attention for their potential to revolutionize technologies in the material fields (engineering, biomedical, and sensors) and synthetic design strategies as they provide access to stimuli responsiveness and adaptive behaviors. However, only a limited number of molecular motifs have been known to display this dynamic behavior under mild conditions. Here, we identified a dynamic covalent motif - thioaminals - that is produced from the reaction of hexahydrotriazines (HTs) with thiols. Furthermore, we report on the synthesis of a new family of step-growth polymers based on this motif. The condensation efficiently proceeds to quantitative yields within a short time frame and offers versatility in functional group tolerance; thus, it can be exploited to synthesize both small molecule thioaminals as well as high molecular weight polymers from the step-growth polymerization of HTs with dithiols. Careful evaluation of substituted HTs and organic thiols supported by DFT calculations led to a chemically diverse library of polymers based on this motif. Finally, dynamic substitution reactions were employed toward the facile preparation of functional oligomers and macromolecules. This dynamic covalent motif is particularly attractive for a range of applications that include material design and drug delivery due to the economic feasibility of synthesis.

Nickel Boride Catalyzed Reductions of Nitro Compounds and Azides: Nanocellulose-Supported Catalysts in Tandem Reactions

Proietti, Giampiero,Prathap, Kaniraj Jeya,Ye, Xinchen,Olsson, Richard T.,Dinér, Peter

, p. 133 - 146 (2021/11/04)

Nickel boride catalyst prepared in situ from NiCl2 and sodium borohydride allowed, in the presence of an aqueous solution of TEMPO-oxidized nanocellulose (0.01 wt%), the reduction of a wide range of nitroarenes and aliphatic nitro compounds. Here we describe how the modified nanocellulose has a stabilizing effect on the catalyst that enables low loading of the nickel salt pre-catalyst. Ni-B prepared in situ from a methanolic solution was also used to develop a greener and facile reduction of organic azides, offering a substantially lowered catalyst loading with respect to reported methods in the literature. Both aromatic and aliphatic azides were reduced, and the protocol is compatible with a one-pot Boc-protection of the obtained amine yielding the corresponding carbamates. Finally, bacterial crystalline nanocellulose was chosen as a support for the Ni-B catalyst to allow an easy recovery step of the catalyst and its recyclability for new reduction cycles.

Synthesis and characterization of polyaniline/nickel oxide composites for fuel additive and dyes reduction

Jamil, Saba,Ahmad, Zunaira,Ali, Muhammad,Rauf Khan, Shanza,Ali, Sarmed,Amen Hammami, Mohamed,Haroon, Muhammad,Saleh, Tawfik A.,Ramzan Saeed Ashraf Janjua, Muhammad

, (2021/05/13)

Polyaniline (PANI) and Polyaniline/Nickel oxide (PANI/NiO) composites are prepared to use as a potential catalyst, by Chemical oxidation method using ammonium persulfate (NH4)2S2O8)) as an oxidant. Nickel oxide (NiO) nanopartiles are prepared by Sol-gel method. The synthesized products were characterized by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray analysis (EDX), Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffraction technique (XRD). The prepared PANI/NiO composites are used as additive with different concentrations in diesel to investigate their efficiency as fuel additive. The catalytic properties are studied by using the synthesized products as catalyst for reduction of dyes in aqueous media. Sodium borohydride (NaBH4) is used as reducing agent. Linear relationships are obtained between time and ln(A0/At) for Methyl orange and Methylene blue. Kapp values were obtained for three catalysts showed the increasing trend of reduction for both dyes as, PANI NiO PANI/NiO composites. Experimental data analysis proved PANI/NiO composites to be efficient catalysts and fuel additive as compared to PANI and NiO.

Development of sustainable and efficient nanocatalyst based on polyoxometalate/nickel oxide nanocomposite: A simple and recyclable catalyst for reduction of nitroaromatic compounds

Kurbah, Sunshine Dominic

, p. 1487 - 1495 (2021/04/22)

In this paper, we report the synthesis and characterization of NiO@PolyMo nanocomposite. The newly synthesized nanocomposite was characterized by transmission electronmicroscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and powder X-ray diffraction (XRD). The particle sizes of the NiO@PolyMo nanocatalyst are in the range of 10–20 nm. Powder XRD patterns show that the phase of NiO@PolyMo remains unaltered even after the functionalization of NiO. The lattice fringes of d = 0.20 nm were observed, which correspond to the (111) plane of NiO phase. The newly synthesized material shows excellent catalytic performance and good selectivity for reduction of nitroarenes. The advantages of the present protocols are mild, and can be carried out using water as a solvent, which is an eco-friendly benign.

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