Production Method 1

95-68-1

Reaction Conditions

1.1 Reagents: Phenylsilane Catalysts: Dicobalt octacarbonyl Solvents: Tetrahydrofuran ;  3 h, 100 °C

Reference

Cobalt catalyzed chemoselective reduction of nitroarenes: hydrosilylation under thermal and photochemical reaction conditions

Panda, Surajit; Nanda, Amareshwar; Behera, Rakesh R.; Ghosh, Rahul; Bagh, Bidraha, Chemical Communications (Cambridge, 2023, 59(30), 4527-4530

Production Method 2

164406-61-5

95-68-1

Reaction Conditions

1.1 Reagents: 2-Propanone, O-[(2,4,6-trimethylphenyl)sulfonyl]oxime Catalysts: Cuprous cyanide Solvents: Tetrahydrofuran ;  1.5 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  overnight, rt
1.3 Reagents: Sodium hydroxide Solvents: Water ;  basified, rt

Reference

Electrophilic amination of diarylcadmium reagents: the effect of aminating reagent's structure

Daskapan, Tahir ; Korkmaz, Adem, Journal of Chemical Sciences (Berlin, 2022, 134(4),

Production Method 3

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Cobalt Solvents: Ethanol ,  Methanol ;  2 h, 2 MPa, 60 °C

Reference

In situ-formed cobalt nanoparticles embedded within carbonaceous matrix as highly efficient and selective catalysts for the hydrogenation of nitroarenes

Zhuang, Xiuzheng; Liu, Jianguo; Zhong, Shurong; Ma, Longlong, Sustainable Chemistry and Pharmacy, 2022, 29,

Production Method 4

95-68-1

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: Molybdenum nitride (Mo2N) Solvents: Ethanol ;  1 h, 30 °C

Reference

Mo2N as a high-efficiency catalyst for transfer hydrogenation of nitrobenzene using stoichiometric hydrazine hydrate

Luo, Shicheng; Long, Yu; Liang, Kun; Sun, Xun; Qin, Jiaheng; et al, Molecular Catalysis, 2022, 531,

Production Method 5

95-66-9

95-68-1

Reaction Conditions

1.1 Reagents: Ammonia ,  Tripotassium phosphate Catalysts: Copper ,  2633071-98-2 Solvents: Dimethyl sulfoxide ,  Water ;  48 h, 80 °C

Reference

Porous polymeric ligand promoted copper-catalyzed C-N coupling of (hetero)aryl chlorides under visible-light irradiation

Wang, Erfei; Chen, Kaixuan; Chen, Yinan; Zhang, Jiawei; Lin, Xinrong; et al, Science China: Chemistry, 2021, 64(1), 17-21

Production Method 6

95-68-1

Reaction Conditions

1.1 Reagents: Oxygen ,  Hydrazine hydrate (1:1) Catalysts: Molybdenum nitrogen oxide ,  Carbon nitride (C3N4) Solvents: Ethanol ;  1 h, 30 °C

Reference

Unsaturated Mo in Mo4O4N3 for efficient catalytic transfer hydrogenation of nitrobenzene using stoichiometric hydrazine hydrate

Luo, Shicheng; Long, Yu; Liang, Kun; Qin, Jiaheng; Qiao, Yi; et al, Green Chemistry, 2021, 23(21), 8545-8553

Production Method 7

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Carbon Solvents: Methanol ,  Water ;  3 h, 5 bar, 90 °C

Reference

Co,N-Codoped Porous Carbon-Supported CoyZnS with Superior Activity for Nitroarene Hydrogenation

Zhang, Guangji; Tang, Feiying; Wang, Xiaoying; An, Ping; Wang, Liqiang ; et al, ACS Sustainable Chemistry & Engineering, 2020, 8(15), 6118-6126

Production Method 8

31516-11-7

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Potassium tert-butoxide ,  Manganese, bromodicarbonyl[6-[(diphenylphosphino-κP)methyl]-2,2′-bipyridine-κN1,… Solvents: Toluene ;  48 h, 20 bar, 130 °C; 130 °C → 0 °C; 30 min, 0 °C

Reference

Manganese Catalyzed Hydrogenation of Carbamates and Urea Derivatives

Das, Uttam Kumar ; Kumar, Amit; Ben-David, Yehoshoa; Iron, Mark A. ; Milstein, David, Journal of the American Chemical Society, 2019, 141(33), 12962-12966

Production Method 9

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethanol ;  1.25 h, 1 atm, rt

Reference

Green reusable Pd nanoparticles embedded in phytochemical resins for mild hydrogenations of nitroarenes

Enneiymy, Mohamed; Le Drian, Claude; Becht, Jean-Michel, New Journal of Chemistry, 2019, 43(44), 17383-17389

Production Method 10

95-68-1

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: Cobalt oxide (titanium oxide supported) Solvents: Ethanol ;  24 h

Reference

Photocatalytic hydrogenation of nitroarenes: supporting effect of CoOx on TiO2 nanoparticles

Amanchi, Srinivasa Rao; Ashok Kumar, K. V.; Lakshminarayana, Bhairi; Satyanarayana, G.; Subrahmanyam, Ch., New Journal of Chemistry, 2019, 43(2), 748-754

Production Method 11

95-68-1

Reaction Conditions

1.1 Reagents: Lithium hydroxide ,  Hydrazine hydrate (1:1) Catalysts: Palladium Solvents: 1,4-Dioxane ;  20 min, rt; 16 h, 170 °C

Reference

Direct conversion of phenols into primary anilines with hydrazine catalyzed by palladium

Qiu, Zihang; Lv, Leiyang; Li, Jianbin; Li, Chen-Chen; Li, Chao-Jun, Chemical Science, 2019, 10(18), 4775-4781

Production Method 12

2050-43-3

95-68-1

1742-94-5

Reaction Conditions

1.1 Reagents: Formic acid ,  Triethylamine Catalysts: Ruthenium, [(1,2,5,6-η)-1,5-cyclooctadiene]bis[(1,2,3-η)-2-methyl-2-propenyl]- ,  Triphos ,  Bis(trifluoromethanesulfonyl)imide Solvents: Butyl ether ;  24 h, 130 °C

Reference

Ru-Catalyzed Deoxygenative Transfer Hydrogenation of Amides to Amines with Formic acid/Triethylamine

Pan, Yixiao; Luo, Zhenli; Xu, Xin; Zhao, Haoqiang; Han, Jiahong; et al, Advanced Synthesis & Catalysis, 2019, 361(16), 3800-3806

Production Method 13

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Dimethylformamide ;  8 h, 0.6 MPa, 120 °C

Reference

Solvent-Driven Selectivity Control to Either Anilines or Dicyclohexylamines in Hydrogenation of Nitroarenes over a Bifunctional Pd/MIL-101 Catalyst

Chen, Xiaodong; Shen, Kui ; Ding, Danni; Chen, Junying; Fan, Ting ; et al, ACS Catalysis, 2018, 8(11), 10641-10648

Production Method 14

95-68-1

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: Molybdenum oxide (MoO3) (cobalt and N-doped graphite, supported on SBA-15) ,  Cobalt (molybdenum oxide and N-doped graphitic carbon, supported on SBA-15) ,  Silica Solvents: Ethanol ;  60 min, 30 °C

Reference

N-doped graphitic carbon-improved Co-MoO3 catalysts on ordered mesoporous SBA-15 for chemoselective reduction of nitroarenes

Huang, Haigen; Liang, Xiangcheng; Wang, Xueguang; Sheng, Yao; Chen, Chenju; et al, Applied Catalysis, 2018, 559, 127-137

Production Method 15

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Nickel Solvents: Water ;  2.5 h, 5 MPa, 100 °C

Reference

Nitrogen-doped graphene-activated metallic nanoparticle-incorporated ordered mesoporous carbon nanocomposites for the hydrogenation of nitroarenes

Huang, Haigen; Wang, Xueguang; Sheng, Yao; Chen, Chenju; Zou, Xiujing; et al, RSC Advances, 2018, 8(16), 8898-8909

Production Method 16

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen ,  Hydrazine hydrate (1:1) Catalysts: Hexadecyl-3-methylimidazolium bromide (Ruthenium supported) Solvents: Ethanol ;  2 h, 2 MPa, 40 °C

Reference

Preparation of Well-Ordered Mesoporous-Silica-Supported Ruthenium Nanoparticles for Highly Selective Reduction of Functionalized Nitroarenes through Transfer Hydrogenation

Wei, Ning; Zou, Xiujing; Huang, Haigen; Wang, Xueguang; Ding, Weizhong; et al, European Journal of Organic Chemistry, 2018, 2018(2), 209-214

Production Method 17

70314-82-8

1613-86-1

95-68-1

312633-84-4

Reaction Conditions

1.1 Reagents: Sodium hydride Catalysts: Titania Solvents: Tetrahydrofuran ;  1 h, rt

Reference

TiO2-Nanoparticles Catalyzed Synthesis of New Trifluoromethyl-4,5-dihydro-1,2,4-oxadiazoles and Trifluoromethyl-1,2,4-oxadiazoles

Darehkordi, Ali ; Ramezani, Mahin; Rahmani, Fariba, Journal of Heterocyclic Chemistry, 2018, 55(7), 1702-1708

Production Method 18

95-68-1

Reaction Conditions

1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: Molybdenum oxide (MoO3) (NiO/SBA-15 supported) ,  Nickel monoxide (MoO3/SBA-15 supported) Solvents: Ethanol ;  30 min, 40 °C

Reference

Highly chemoselective reduction of nitroarenes over non-noble metal nickel-molybdenum oxide catalysts

Huang, Haigen; Wang, Xueguang; Li, Xu; Chen, Chenju; Zou, Xiujing; et al, Green Chemistry, 2017, 19(3), 809-815

Production Method 19

2050-43-3

95-68-1

1742-94-5

Reaction Conditions

1.1 Reagents: Tris(pentafluorophenyl)borane ,  Hydrogen Catalysts: Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate ,  (SP-5-43)-[2,6-Bis[[bis(1-methylethyl)phosphino-κP]oxy]phenyl-κC]chlorohydroirid… Solvents: Toluene ;  24 h, 50 atm, 120 °C

Reference

Deoxygenative Hydrogenation of Amides Catalyzed by a Well-Defined Iridium Pincer Complex

Yuan, Ming-Lei; Xie, Jian-Hua; Zhu, Shou-Fei; Zhou, Qi-Lin, ACS Catalysis, 2016, 6(6), 3665-3669

Production Method 20

95-68-1

Reaction Conditions

1.1 Reagents: Sodium borohydride Catalysts: Nickel ,  Silica Solvents: Water ;  65 min, rt

Reference

Preparation and characterization of Ni/mZSM-5 zeolite with a hierarchical pore structure by using KIT-6 as silica template: an efficient bi-functional catalyst for the reduction of nitro aromatic compounds

Mazaheri, Omid; Kalbasi, Roozbeh Javad, RSC Advances, 2015, 5(43), 34398-34414

Production Method 21

95-68-1

Reaction Conditions

Reference

Hydroxylamine-mediated C-C amination via an aza-hock rearrangement

Wang, Tao; Stein, Philipp M.; Shi, Hongwei; Hu, Chao; Rudolph, Matthias; et al, Nature Communications, 2021, 12(1),

Production Method 22

95-68-1

Reaction Conditions

1.1 Reagents: Sodium borohydride Catalysts: Ruthenium Solvents: Ethanol ,  Water ;  240 min, rt

Reference

A One-Step Method for Preparation of Ru Nanoparticle Decorated on Three-Dimensional Graphene with High Catalytic Activity for Reduction of Nitroarenes

Dabiri, Minoo; Miraghaee, Seyedesahar; Nikbakht, Roonak; Bashiribod, Sahareh, Journal of Cluster Science, 2021, 32(4), 959-965

Production Method 23

95-68-1

Reaction Conditions

1.1 Reagents: Phenylsilane Catalysts: Triphenylphosphine ,  Sodium iodide Solvents: Chloroform ;  72 h, 60 °C
1.2 Reagents: Sodium carbonate Solvents: Water

Reference

NaI/PPh3-Mediated Photochemical Reduction and Amination of Nitroarenes

Qu, Zhonghua; Chen, Xing; Zhong, Shuai; Deng, Guo-Jun ; Huang, Huawen, Organic Letters, 2021, 23(14), 5349-5353

Production Method 24

95-68-1

87-62-7

108-69-0

Reaction Conditions

1.1 Reagents: Hydroxyamine hydrochloride ,  Sulfuric acid Solvents: Acetonitrile ;  25 °C; 10 min, 25 °C
1.2 Reagents: Hydrochloric acid ,  Titanium chloride (TiCl3) Solvents: Water ;  25 °C; 10 min, 25 °C
1.3 Reagents: Citric acid, sodium salt ,  Sodium hydroxide Solvents: Water ;  basified, 25 °C

Reference

C-H Amination of Arenes with Hydroxylamine

See, Yi Yang; Sanford, Melanie S., Organic Letters, 2020, 22(8), 2931-2934

Production Method 25

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethanol ;  2 h, 1 atm, rt

Reference

Palladium nanoparticles embedded in mesoporous carbons as efficient, green and reusable catalysts for mild hydrogenations of nitroarenes

Enneiymy, Mohamed; Fioux, Philippe; Le Drian, Claude; Matei Ghimbeu, Camelia; Becht, Jean-Michel, RSC Advances, 2020, 10(60), 36741-36750

Production Method 26

95-68-1

Reaction Conditions

1.1 Reagents: Potassium carbonate ,  Sulfur ,  Water Solvents: Dimethylformamide ;  20 h, 150 °C

Reference

Metal-free chemoselective reduction of nitroaromatics to anilines via hydrogen transfer strategy

Shuai, Qi; Li, Jun; Zhao, Feng; Su, Weike ; Deng, Guojun, Chemical Papers, 2019, 73(4), 965-975

Production Method 27

33089-61-1

95-68-1

2713973-21-6

Reaction Conditions

1.1 Reagents: Sodium hydroxide ;  10 min, 80 °C

Reference

Chromogenic spray reagent for the detection and identifi cation of amitraz in biological materials

Mulani, Khudbudin B.; Kamble, Brahmanand M.; Chandegaonkar, Vijay R.; Deshpande, Hemantini A., Journal of Planar Chromatography--Modern TLC, 2019, 32(1), 51-53

Production Method 28

95-68-1

Reaction Conditions

1.1 Catalysts: Iron ,  Copper ,  Cellulose Solvents: Water ;  5 min, rt
1.2 Reagents: Sodium borohydride ;  7 h, 70 °C

Reference

Cellulose supported bimetallic Fe-Cu nanoparticles: a magnetically recoverable nanocatalyst for quick reduction of nitroarenes to amines in water

Karami, Shiva; Zeynizadeh, Behzad; Shokri, Zahra, Cellulose (Dordrecht, 2018, 25(6), 3295-3305

Production Method 29

95-68-1

Reaction Conditions

1.1 Reagents: Ammonium formate Catalysts: Palladium Solvents: Ethanol ;  12 h, rt

Reference

Highly efficient reduction of nitro compounds: recyclable Pd/C-catalyzed transfer hydrogenation with ammonium formate or hydrazine hydrate as hydrogen source

Chen, Xia; Zhou, Xiao-Yu; Wu, Hong; Lei, Yi-Zhu; Li, Jin-Hui, Synthetic Communications, 2018, 48(19), 2475-2484

Production Method 30

95-68-1

Reaction Conditions

Reference

Synthesis, characterization, anticancer and antifungal studies of Pyrazole carboxamide derivatives

Sa, Adinarayana; Chauhana, Pramod K.; Choudhary, Prakash C., Chemistry & Biology Interface, 2018, 8(1), 26-44

Production Method 31

95-68-1

Reaction Conditions

Reference

Synthesis, biological evaluation, and in silico study of some unique multifunctional 1,2,4-triazole acetamides

Sattar, Almas; Ur Rehman, Aziz; Abbasi, Muhammad Athar; Siddiqui, Sabahat Zahra; Rasool, Shahid; et al, Turkish Journal of Chemistry, 2018, 42(2), 401-417

Production Method 32

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Ceria ,  Palladium (cerium dioxide-supported) ;  3.5 h, 2 MPa, 45 °C

Reference

High Performance and Active Sites of a Ceria-Supported Palladium Catalyst for Solvent-Free Chemoselective Hydrogenation of Nitroarenes

Shi, Xiuxiu; Wang, Xueguang; Shang, Xingfu; Zou, Xiujing; Ding, Weizhong; et al, ChemCatChem, 2017, 9(19), 3743-3751

Production Method 33

95-68-1

87-62-7

Reaction Conditions

1.1 Reagents: Trifluoromethanesulfonic acid ,  Azidotrimethylsilane Solvents: Methanol ,  Chloroform ;  2.7 min, 90 °C
1.2 Reagents: Methanol ;  90 °C
1.3 Reagents: Sodium bicarbonate Solvents: Water ;  neutralized, rt

Reference

Continuous-Flow Electrophilic Amination of Arenes and Schmidt Reaction of Carboxylic Acids Utilizing the Superacidic Trimethylsilyl Azide/Triflic Acid Reagent System

Chen, Yuesu; Gutmann, Bernhard; Kappe, C. Oliver, Journal of Organic Chemistry, 2016, 81(19), 9372-9380

Production Method 34

95-68-1

Reaction Conditions

Reference

Synthesis of 2-{(5-phenyl-l,3,4-Oxadiazol-2-yl)sulfanyl}_N-substituted acetamides as potential antimicrobial and hemolytic agents

Aziz-ur-Rehman; Abbasi, Muhammad Athar; Siddiqui, Sabahat Zahra; Ahmad, Irshad; Shahid, Muhammad; et al, Pakistan Journal of Pharmaceutical Sciences, 2016, 29(3), 801-809

Production Method 35

95-68-1

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium (nanoclusters, nitrogen-doped mesoporous carbon-supported) ;  2 h, 1 MPa, rt → 45 °C

Reference

Solvent-Free Selective Hydrogenation of Nitroarenes Using Nanoclusters of Palladium Supported on Nitrogen-Doped Ordered Mesoporous Carbon

Huang, Haigen; Wang, Xueguang; Tan, Mingwu; Chen, Chenju; Zou, Xiujing; et al, ChemCatChem, 2016, 8(8), 1485-1489

Production Method 36

95-68-1

Reaction Conditions

1.1 Reagents: Pyridine ,  Tetrabutylammonium tetrafluoroborate Solvents: Acetonitrile ;  22 °C
1.2 Reagents: Piperidine ;  12 h, 80 °C

Reference

Electrochemical Amination of Less-Activated Alkylated Arenes Using Boron-Doped Diamond Anodes

Herold, Sebastian; Moehle, Sabine; Zirbes, Michael; Richter, Frank; Nefzger, Hartmut; et al, European Journal of Organic Chemistry, 2016, 2016(7), 1274-1278

Production Method 37

29418-25-5

95-68-1

41825-73-4

Reaction Conditions

1.1 Reagents: Cuprous iodide ,  Hydrogen bromide Solvents: 1,2-Dichloroethane ,  Water ;  12 h, 120 °C

Reference

Copper-Promoted Tandem Reaction of Azobenzenes with Allyl Bromides via N=N Bond Cleavage for the Regioselective Synthesis of Quinolines

Yi, Xiangli; Xi, Chanjuan, Organic Letters, 2015, 17(23), 5836-5839

Production Method 38

95-68-1

Reaction Conditions

1.1 Reagents: Thiourea ,  Potassium tert-butoxide Solvents: Ethanol ;  12 h, 80 °C

Reference

Catalyst-Free Chemoselective Reduction of Nitroarenes Using Thiourea as a Hydrogen Source

Lv, Mei-fang; Lu, Guo-ping; Cai, Chun, Asian Journal of Organic Chemistry, 2015, 4(2), 141-144

Production Method 39

95-68-1

Reaction Conditions

1.1 Reagents: Oxygen ,  Poly(methylhydrosiloxane) Catalysts: Bis(acetylacetonato)nickel Solvents: 1,4-Dioxane ;  3 - 5 h, 80 °C

Reference

Selective reduction of nitro-compounds to primary amines by nickel-catalyzed hydrosilylative reduction

Sun, Shuai; Quan, Zhengjun; Wang, Xicun, RSC Advances, 2015, 5(103), 84574-84577

Production Method 40

95-68-1

Reaction Conditions

1.1 Reagents: Ammonium formate Catalysts: 1604839-72-6 (silica-coated iron oxide-bound) Solvents: Water ;  20 h, 90 °C

Reference

A Highly Water-Dispersible/Magnetically Separable Palladium Catalyst: Selective Transfer Hydrogenation or Direct Reductive N-Formylation of Nitroarenes in Water

Karimi, Babak; Mansouri, Fariborz; Vali, Hojatollah, ChemPlusChem, 2015, 80(12), 1750-1759

2,4-dimethylaniline Raw materials

• N-(2,4-dimethylphenyl)-2,2,2-trifluoroacetimidoyl chloride
• Diazene,1,2-bis(2,4-dimethylphenyl)-
• N-Hydroxy-4-nitrobenzimidamide
• 1,3-Bis(2,4-dimethylphenyl)urea
• Bis(2,4-dimethylphenyl)cadmium
• N-(2,4-Dimethylphenyl)acetamide
• 4-Chloro-m-xylene
• Amitraz

2,4-dimethylaniline Preparation Products

• 2,4-dimethylaniline (95-68-1)
• N′-(2,4-Dimethylphenyl)-N-formyl-N-methylmethanimidamide (2713973-21-6)
• 2,6-Dimethylaniline (87-62-7)
• 3,5-Dimethylaniline (108-69-0)
• 2-Bromo-4,6-dimethylaniline (41825-73-4)
• N-ethyl-2,4-dimethylaniline (1742-94-5)
• 1,2,4-Oxadiazole, 3-(4-nitrophenyl)-5-(trifluoromethyl)- (312633-84-4)

• 1. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
• 2. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 3. Fe(iii)-mediated isomerization of α,α-diarylallylic alcohols to ketones via radical 1,2-aryl migration?
  Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
• 4. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 5. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives m-Xylenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Xylenes m-Xylenes
• Pesticide Chemicals Pesticide Active Ingredients Standard Substances
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides

• 919785-81-2(2,6-Dimethylaniline-D6)
• 78288-65-0(Benzenamine, 2,4-dimethyl-, ion(1-) (9CI))
• 82299-97-6(Benzenamine,2-(methyl-14C)- (9CI))
• 88-05-1(2,4,6-Trimethylaniline (Mesidine), ND25=1,4959)
• 151985-13-6(o-Toluidine-d3 (methyl-d3))
• 68408-20-8(O-TOLUIDINE-4,6-D2)
• 68408-22-0(2-TOLUIDINE-D7)
• 87-62-7(2,6-Dimethylaniline)
• 194423-47-7(2-Toluidine-d9)
• 1092805-08-7(2,6-DIMETHYLANILINE-D11)