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768-52-5

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768-52-5 Usage

Chemical Properties

Clear light yellow liquid

Uses

Different sources of media describe the Uses of 768-52-5 differently. You can refer to the following data:
1. Dyeing acrylic fibers, chemical intermediate.
2. Dyeing of acrylic fibers and as a chemical intermediate
3. N-Isopropylaniline is a microbial metabolite of Propachlor (P757300), an acylanilide herbicide that is used to maintain crop protection from weeds. Propachlor is also known to induce Glutathione (G597951)-dependent cytotoxicity and sister chromatid exchanges in human cells.

Synthesis Reference(s)

The Journal of Organic Chemistry, 28, p. 3259, 1963 DOI: 10.1021/jo01046a537Tetrahedron, 52, p. 9777, 1996 DOI: 10.1016/0040-4020(96)00503-0

Air & Water Reactions

Insoluble in water.

Reactivity Profile

N-Isopropylaniline 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.

Hazard

Toxic by inhalation and skin absorption.

Health Hazard

N-isopropylaniline absorption causes methemoglobinemia in animals, and the same effect is expected in humans.

Fire Hazard

N-Isopropylaniline is combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 768-52-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 768-52:
(5*7)+(4*6)+(3*8)+(2*5)+(1*2)=95
95 % 10 = 5
So 768-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N/c1-8(2)10-9-6-4-3-5-7-9/h3-8,10H,1-2H3

768-52-5 Well-known Company Product Price

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

  • (L10646)  N-Isopropylaniline, 98%   

  • 768-52-5

  • 10g

  • 402.0CNY

  • Detail
  • Alfa Aesar

  • (L10646)  N-Isopropylaniline, 98%   

  • 768-52-5

  • 50g

  • 1389.0CNY

  • Detail
  • Sigma-Aldrich

  • (31576)  N-Isopropylaniline  PESTANAL®, analytical standard

  • 768-52-5

  • 31576-1G

  • 329.94CNY

  • Detail

768-52-5SDS

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-Isopropylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine, N-(1-methylethyl)-

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:768-52-5 SDS

768-52-5Relevant articles and documents

Efficient reductive alkylation of aniline with acetone over Pt nanoparticles encapsulated in hollow porous carbon

Harada, Takashi,Ikeda, Shigeru,Okamoto, Natsumi,Ng, Yun Hau,Higashida, Suguru,Torimoto, Tsukasa,Matsumura, Michio

, p. 948 - 949 (2008)

Reductive alkylation of aniline with acetone over various Pt catalysts was studied under atmospheric pressure of hydrogen at room temperature. It was found that our newly designed Pt catalyst, i.e., Pt nanoparticles encapsulated in hollow porous carbon, showed excellent catalytic activity in comparison with activities of other Pt catalysts. Moreover, one-pot reductive alkylation of nitrobenzene with acetone proceeded smoothly over the catalyst. Copyright

CO2-tuned highly selective reduction of formamides to the corresponding methylamines

Chao, Jianbin,Guo, Zhiqiang,Pang, Tengfei,Wei, Xuehong,Xi, Chanjuan,Yan, Leilei

supporting information, p. 7534 - 7538 (2021/10/12)

We herein describe an efficient, CO2-tuned and highly selective C-O bond cleavage of N-methylated formanilides. With easy-to-handle and commercially available NaBH4 as the reductant, a variety of formanilides could be turned into the desired tertiary amines in moderate to excellent yields. The role of CO2 has been investigated in detail, and the mechanism is proposed on the basis of experiments.

A Highly Dispersed Copper Nanoparticles Catalyst with a Large Number of Weak Acid Centers for Efficiently Synthesizing the High Value-Added 3-Methylindole by Aniline and Biomass-Derived Glycerin

Sun, Pinghui,Lin, Shuyi,Guo, Huimei,Su, Jianhui,Shi, Lei

, p. 463 - 477 (2020/07/16)

Abstract: An excellent catalyst with a large number of weak acid centers and highly dispersed copper nanoparticles embedded in mesoporous SBA-15 carrier was successfully constructed for the purpose of efficient conversion of aniline with biomass-derived glycerin to the high value-added 3-methylindole, in which the catalyst of Cu/SBA-15 was modified with Al2O3, La2O3 and CoO in sequence. The modified carrier and the copper-based catalysts were studied by scanning electron microscopy and energy-dispersive X-ray (SEM–EDX) spectroscopy, nitrogen physical adsorption, ammonia temperature programmed desorption (NH3-TPD), hydrogen temperature programmed reduction (H2-TPR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric and differential thermal analysis (TG–DTA) and inductively coupled plasma (ICP) emission spectroscopy. The research found that the Cu/CoO/La2O3/Al2O3/SBA-15 catalyst exhibited a very good catalytic performance with 3-methylindole yield up to 73.3% and selectivity reaching 86.4%. Besides, only a 3.9% yield decreased after the catalyst was circulated seven times. The characterizations revealed that Al2O3 could enhance the polarity of the carrier, thereby the interaction between the active component and the composite carrier was strengthened and the dispersion of copper was increased significantly. Adding La2O3 to Cu/SBA-15-Al2O3 could weaken the acidity and inhibit the formation of carbon deposits. CoO promoter could increase the number of weak acid centers, which was conducive to a good dispersion of active component and the high selectivity of 3-methylindole. Furthermore, the reaction pathway of gas-phase synthesis of 3-methylindole from glycerin and aniline on Cu/CoO/La2O3/Al2O3/SBA-15 was explored. Graphic Abstract: [Figure not available: see fulltext.]

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