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3,4-Dimethyl-o-phenylenediamine is an aromatic amine chemical compound known for its ability to penetrate the hair shaft and produce long-lasting color. It is commonly used as a raw material in the production of hair dyes and other hair coloring products. However, it is also associated with certain health concerns, such as skin irritation, allergic reactions, and potential carcinogenic effects, leading to regulations and guidelines regarding its use and concentration in hair coloring products.

41927-01-9

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41927-01-9 Usage

Uses

Used in Hair Coloring Industry:
3,4-Dimethyl-o-phenylenediamine is used as a raw material in the production of hair dyes and other hair coloring products for its ability to easily penetrate the hair shaft and produce long-lasting color. However, due to its potential health risks, there are regulations and guidelines in place to ensure its safe use and appropriate concentration in these products.

Check Digit Verification of cas no

The CAS Registry Mumber 41927-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,2 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41927-01:
(7*4)+(6*1)+(5*9)+(4*2)+(3*7)+(2*0)+(1*1)=109
109 % 10 = 9
So 41927-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-5-3-4-7(9)8(10)6(5)2/h3-4H,9-10H2,1-2H3

41927-01-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L07455)  3,4-Dimethyl-o-phenylenediamine, 98%   

  • 41927-01-9

  • 1g

  • 650.0CNY

  • Detail
  • Alfa Aesar

  • (L07455)  3,4-Dimethyl-o-phenylenediamine, 98%   

  • 41927-01-9

  • 5g

  • 2329.0CNY

  • Detail

41927-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethylbenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1,2-Benzenediamine, 3,4-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:41927-01-9 SDS

41927-01-9Relevant academic research and scientific papers

Catalytic Reduction of Nitroarenes by Dipalladium Complexes: Synergistic Effect

Yang, Shu-Ting,Shen, Peng,Liao, Bei-Sih,Liu, Yi-Hung,Peng, Shie-Ming,Liu, Shiuh-Tzung

supporting information, p. 3110 - 3116 (2017/09/05)

The direct reaction between 2,7-bis(2-pyridinyl)-1,8-naphthyridine (bpnp) and Pd(CH3COO)2 in CF3COOH yields the new dinuclear palladium(II) complex [Pd2(bpnp)(μ-OH)(CF3CO2)2](CF3CO2) (1). Similarly, substitution of Pd(CH3CN)4(BF4)2 with bpnp in DMF gives [Pd2(bpnp)(μ-OH)(DMF)2](BF4)3 (2). Treatment of 1 or 2 with Cl- readily provide the chloro-substituted species [Pd(bpnp)(μ-OH)(Cl)2]+. All complexes were characterized by spectroscopic methods, and the structure of 2 was further confirmed by X-ray crystallography. Complex 1 is an efficient catalyst for the reduction of aromatic nitro compounds leading to the corresponding aniline derivatives under atmospheric pressure of hydrogen at 50 °C. The mechanistic pathway of the catalysis is investigated. From the reaction pathway, it is suggested that a facile condensation of nitroso and hydroxylamine intermediates is enabled by the dipalladium system and the desired transformation proceeds smoothly under mild reaction conditions to yield the reduced product.

Iridium catalyst complexes and C—H bond activated products therefrom

-

, (2016/04/20)

Provided is a novel iridium catalyst complex which is useful in the dehydrogenation of alkanes. The iridium complex comprises the metal iridium atom complexed with a benzimidazolyl-containing ligand. The iridium atom can be coordinated with the nitrogen a

Process for Alkane Oligomerization

-

Paragraph 0042, (2013/04/13)

Provided is a process for preparing oligomers from an alkane. The process comprises (a) contacting an alkane under dehydrogenation conditions in the presence of a dehydrogenation catalyst such as an iridium catalyst complex comprising iridium complexed with a benzimidiazolyl-containing ligand to form olefins, and (b) contacting the olefins prepared in step (a) under oligomerization conditions with an oligomerization catalyst such as a nickel, platinum or palladium metal catalyst complex comprising the metal complexed with a nitrogen containing bi- or tridentate ligand to prepare oligomers of the olefins, and hydrogenating the olefin oligomers. In one embodiment, the ligands of the catalyst complexes in step (a) and step (b) can be the same.

Urea and thiourea derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists

-

, (2008/06/13)

A novel series of substituted quinoxaline 2,3-diones useful as neuroprotective agents are taught. Novel intermediates, processes of preparation, and pharmaceutical compositions containing the compounds are also taught. The compounds are glutamate antagonists and are useful in the treatment of stroke, cerebral ischemia, or cerebral infarction resulting from thromboembolic or hemorrhagic stroke, cerebral vasospasms, hypoglycemia, cardiac arrest, status epilepticus, perinatal asphyxia, anoxia, seizure disorders, pain, Alzheimer''s, Parkinson''s, and Huntington''s Diseases.

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