Welcome to LookChem.com Sign In|Join Free

Cas Database

121-73-3

121-73-3

Identification

  • Product Name:Benzene,1-chloro-3-nitro-

  • CAS Number: 121-73-3

  • EINECS:204-496-1

  • Molecular Weight:157.556

  • Molecular Formula: C6H4ClNO2

  • HS Code:29049085

  • Mol File:121-73-3.mol

Synonyms:1-Chloro-3-nitrobenzene;3-Chloro-1-nitrobenzene;3-Chloronitrobenzene;3-Nitro-1-chlorobenzene;3-Nitrophenyl chloride;NSC 5502;m-Chloronitrobenzene;m-Nitrochlorobenzene;

Post Buying Request Now
Entrust LookChem procurement to find high-quality suppliers faster

Safety information and MSDS view more

  • Pictogram(s):ToxicT,HarmfulXn,DangerousN

  • Hazard Codes:Xn,N,T

  • Signal Word:Danger

  • Hazard Statement:H301 Toxic if swallowedH311 Toxic in contact with skin H317 May cause an allergic skin reaction H331 Toxic if inhaled H411 Toxic to aquatic life with long lasting effects

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled Fresh air, rest. Refer for medical attention. See Notes. In case of skin contact Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention . In case of eye contact Rinse with plenty of water for several minutes (remove contact lenses if easily possible). If swallowed Rinse mouth. Refer immediately for medical attention. SYMPTOMS: Symptoms of exposure to this compound may include cyanosis from methemoglobinemia; and blood changes. ACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits toxic fumes. /SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . /Aromatic hydrocarbons and related compounds/

  • Fire-fighting measures: Suitable extinguishing media Water may cause foaming or frothing. Use water spray, dry chemical, foam, or carbon dioxide. /Chloronitrobenzenes/ Flash point data for this chemical are not available. It is probably combustible. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Do NOT let this chemical enter the environment. Sweep spilled substance into sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations. Environmental considerations-land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Cover solids with a plastic sheet to prevent dissolving in rain or fire fighting water. Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, or commercial sorbents. /Chloronitrobenzenes, meta, solid/

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Separated from combustible substances, reducing agents and food and feedstuffs. Store in an area without drain or sewer access. Provision to contain effluent from fire extinguishing.Store in a cool, dry, well ventilated location. Separate from alkalies and oxidizing materials. /Chloronitrobenzenes/

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

  • Manufacture/Brand
  • Product Description
  • Packaging
  • Price
  • Delivery
  • Purchase
  • Manufacture/Brand:TCI Chemical
  • Product Description:1-Chloro-3-nitrobenzene >99.0%(GC)
  • Packaging:25g
  • Price:$ 16
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:TCI Chemical
  • Product Description:1-Chloro-3-nitrobenzene >99.0%(GC)
  • Packaging:500g
  • Price:$ 82
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:1-Chloro-3-nitrobenzene 98%
  • Packaging:250g
  • Price:$ 42.1
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Frontier Specialty Chemicals
  • Product Description:1-Chloro-3-nitrobenzene 98%
  • Packaging:25g
  • Price:$ 13
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Frontier Specialty Chemicals
  • Product Description:1-Chloro-3-nitrobenzene 98%
  • Packaging:100g
  • Price:$ 24
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Alfa Aesar
  • Product Description:1-Chloro-3-nitrobenzene, 98%
  • Packaging:1000g
  • Price:$ 140
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Alfa Aesar
  • Product Description:1-Chloro-3-nitrobenzene, 98%
  • Packaging:250g
  • Price:$ 38.9
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:AK Scientific
  • Product Description:3-Nitrochlorobenzene
  • Packaging:5g
  • Price:$ 14
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:AK Scientific
  • Product Description:3-Nitrochlorobenzene
  • Packaging:5g
  • Price:$ 10
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:AK Scientific
  • Product Description:3-Nitrochlorobenzene
  • Packaging:1g
  • Price:$ 10
  • Delivery:In stock
  • Buy Now

Relevant articles and documentsAll total 92 Articles be found

Superactive iodination reagent on a base of iodine chloride and silver sulfate

Chaikovski, Vitold K.,Kharlova, Tatjana S.,Filimonov, Victor D.,Saryucheva, Tamara A.

, p. 748 - 750 (1999)

After reaction of ICl and Ag2SO4 in sulfuric acid and separation of resulting AgCl a stable solution is formed, containing very active forms of electrophilic iodine. This solution has a powerful iodination ability with respect to aromatic compounds. Deactivated arenes are iodinated easily and in mild conditions by action of this new reagent in generally good yields of the iodoarenes.

Acid-Catalyzed Nucleophilic Aromatic Photosubstitution. A Reconsideration of Protonation in Excited States of Nitrobenzenes

Wubbels, Gene G.,Susens, Douglas P.,Cuoghlin, E. Bryan

, p. 2538 - 2542 (1988)

3-Bromonitrobenzene is photosubstituted inefficiently but cleanly by chloride ion to give 3-chloronitrobenzene.The photosubstitution is catalyzed by hydronium ion; the limiting quantum yield of 0.021 at infinite +> and 3.0 M -> is only 2-fold higher than the quantum yield (0.011) of the uncatalyzed photosubstitution at 3.0 M ->.The limiting quantum yield at infinite chloride ion concentration with no added acid is also 0.021.That 2-propanol does not intervene on the photosubstitution pathway to cause photoreduction indicates that radical intermediates are not involved, and the absence of deuterium incorporation on the aromatic ring accompanying photosubstitution indicates that the catalysis does not involve formation of a dihydrobenzene intermediate.The reaction appears to be an example of the so-called mechanism and the catalysis to be a manifestation of protonation of the 3?,?* state, which is the higher energy triplet state in 3-bromonitrobenzene.

Green route for the chlorination of nitrobenzene

Boltz, Marilyne,De Mattos, Márcio C.S.,Esteves, Pierre M.,Pale, Patrick,Louis, Benoit

, p. 1 - 8 (2012)

A new green chlorination process of deactivated aromatics has been developed, being environmental-friendly and allowing the continuous chlorination of 1.7 kg nitrobenzene/kg catalyst per day. The triple novelty consists of using a non-conventional chlorination agent, the trichloroisocyanuric acid (TCCA, C3N3O3Cl3), along with solid acid catalysts (mainly zeolites) in a continuous flow reactor system. Different zeolites and solid acids have been tested in the chlorination of nitrobenzene, chosen as a model deactivated aromatic substrate. HUSY zeolite was found as the more promising catalyst for performing the chlorination of nitrobenzene, with good conversions (39-64%) at high selectivity toward monochlorinated products (90-99%). Finally, it is worthy to note that HUSY zeolite could be reused for at least five successive runs.

Preparation method of M-nitrochlorobenzene

-

Paragraph 0014-0022, (2021/07/08)

The invention discloses a preparation method of m-nitrochlorobenzene. The method comprises the step of preparing m-nitrochlorobenzene by taking chlorobenzene as a raw material and N-nitropyrazole and H2SO4 as nitrating agents. The method specifically comprises the following steps: adding 8ml of 98% sulfuric acid into a four-neck bottle, dropwise adding 0.012 mol of chlorobenzene into concentrated sulfuric acid under the conditions that the mechanical stirring speed is 300 to 400r/min and the temperature is 20 DEG C, heating in a water bath to 60 DEG C after the charging is completed, averagely dividing 0.024 mol of N-nitropyrazole into four parts, sequentially adding the four parts of N-nitropyrazole at the temperature, heating the reaction system in the charging process, adding materials again after the temperature is reduced to the initial temperature, keeping stirring after the materials are added, reacting at the constant temperature of 65 DEG C for 6 hours, pouring reaction liquid into a container filled with ice blocks while the reaction liquid is hot, and stirring to reduce the temperature of the solution to 5 DEG C to separate out light yellow substances.

Low-temperature and highly efficient liquid-phase catalytic nitration of chlorobenzene with NO2: Remarkably improving the para-selectivity in O2-Ac2O-Hβ composite system

Deng, Renjie,Liu, Pingle,Luo, He'an,Ni, Wenjin,You, Kuiyi,Zhao, Fangfang

, (2020/02/26)

In this work, we developed a low-temperature and efficient approach for the highly selective preparation of valuable p-nitrochlorobenzene from the liquid-phase catalytic nitration of chlorobenzene with NO2 in O2-Ac2O-Hβ composite system. The results demonstrated that the introduction of molecular oxygen remarkably enhanced the chlorobenzene conversion and the cooperation catalysis of Hβ zeolite and Ac2O envidently improved the selectivity to para-nitro product. Under the optimized reaction conditions, 93.6 % of the selectivity to p-nitrochlorobenzene with 84.0 % of chlorobenzene conversion was obtained, and the ratio of p-nitrochlorobenzene to o-nitrochlorobenzene could reach up to 20.3. Furthermore, the selectivity distribution of nitration products was reasonably explained by the density functional theory (DFT) calculation. Finally, the possible nitration reaction pathway of chlorobenzene with NO2 was suggested in O2-Ac2O-Hβ composite catalytic system. The present work affords a new and mild nitration approach for highly selective preparation of valuable para-nitro products, and has potential industrial application prospects.

Synthesis of thioethers, arenes and arylated benzoxazoles by transformation of the C(aryl)-C bond of aryl alcohols

Chen, Bingfeng,Han, Buxing,Liu, Mingyang,Meng, Qinglei,Song, Jinliang,Zhang, Pei,Zhang, Zhanrong

, p. 7634 - 7640 (2020/08/14)

Transformation of aryl alcohols into high-value functionalized aromatic compounds by selective cleavage and functionalization of the C(aryl)-C(OH) bond is of crucial importance, but very challenging by far. Herein, for the first time, we report a novel and versatile strategy for activation and functionalization of C(aryl)-C(OH) bonds by the cooperation of oxygenation and decarboxylative functionalization. A diverse range of aryl alcohol substrates were employed as arylation reagents via the cleavage of C(aryl)-C(OH) bonds and effectively converted into corresponding thioether, arene, and arylated benzoxazole products in excellent yields, in a Cu based catalytic system using O2 as the oxidant. This study offers a new way for aryl alcohol conversion and potentially offers a new opportunity to produce high-value functionalized aromatics from renewable feedstocks such as lignin which features abundant C(aryl)-C(OH) bonds in its linkages.

A convenient room temperature ipso-nitration of arylboronic acid catalysed by molecular iodine using zirconium oxynitrate as nitrating species: An experimental and theoretical investigation

Mahanta, Abhijit,Gour, Nanda Kishor,Sarma, Plaban Jyoti,Borah, Raju Kumar,Raul, Prasanta Kumar,Deka, Ramesh Chandra,Thakur, Ashim Jyoti,Bora, Utpal

, (2019/05/15)

A simple and convenient protocol has been developed for ipso-nitration of arylboronic acid catalysed by molecular iodine at room temperature, using zirconium oxynitrate as the nitrating species. The protocol is applicable to electronically diverse aryl- and heteroarylboronic acid moieties under mild reaction conditions with good to excellent isolated yields. Furthermore, a theoretical investigation has been performed for the same reaction, and reaction profiles are modelled using modern density functional theory (DFT). DFT-based results support the experimentally observed results.

A Predictive Model for the Decarboxylation of Silver Benzoate Complexes Relevant to Decarboxylative Coupling Reactions

Crovak, Robert A.,Hoover, Jessica M.

, p. 2434 - 2437 (2018/02/28)

Decarboxylative coupling reactions offer an attractive route to generate functionalized arenes from simple and readily available carboxylic acid coupling partners, yet they are underutilized due to limitations in the scope of carboxylic acid coupling partner. Here we report that the field effect parameter (F) has a substantial influence on the rate of decarboxylation of well-defined silver benzoate complexes. This finding provides the opportunity to surpass current substrate limitations associated with decarboxylation and to enable widespread utilization of decarboxylative coupling reactions.

Process route upstream and downstream products

Process route

methoxybenzene
100-66-3

methoxybenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
With N-nitro-2,4,6-trimethylpyridinium tetrafluoroborate; In nitromethane; at 25 ℃; Rate constant; competitive nitration with benzene;
nitrobenzene
98-95-3,26969-40-4

nitrobenzene

3,4-dichloronitrobenzene
99-54-7

3,4-dichloronitrobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

1,2-Dichloro-3-nitrobenzene
3209-22-1

1,2-Dichloro-3-nitrobenzene

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

2,5-dichloronitrobenzene
89-61-2

2,5-dichloronitrobenzene

Conditions
Conditions Yield
With chlorine; iron(III) chloride; at 60 - 120 ℃; Product distribution; Kinetics; relative rates of each steps;
nitrobenzene
98-95-3,26969-40-4

nitrobenzene

2,4-dichloronitrobenzene
611-06-3

2,4-dichloronitrobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

Quintozene
82-68-8

Quintozene

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
With chlorine fluorosulfate; In 1,1,2-Trichloro-1,2,2-trifluoroethane; at -25 ℃;
2.8 % Chromat.
8.5 % Chromat.
16.5 % Chromat.
2 g
nitrobenzene
98-95-3,26969-40-4

nitrobenzene

meta-dinitrobenzene
99-65-0

meta-dinitrobenzene

para-dinitrobenzene
100-25-4

para-dinitrobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

1,2-Dinitrobenzene
528-29-0

1,2-Dinitrobenzene

Conditions
Conditions Yield
With hydrogenchloride; sulfuric acid; nitric acid; at 25 ℃; Product distribution;
1.2 % Chromat.
1.3 % Chromat.
96.4 % Chromat.
1.0 % Chromat.
methyl nitrate
598-58-3

methyl nitrate

chlorobenzene
108-90-7

chlorobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
Product distribution; gas-phase radiolytic nitration;
chlorobenzene
108-90-7

chlorobenzene

formic acid
64-18-6

formic acid

2-monochlorophenol
95-57-8

2-monochlorophenol

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

acetic acid
64-19-7,77671-22-8

acetic acid

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
With ozone; hydrazine; at 22.9 ℃; for 0.75h; Product distribution; different reagent concentrations, times;
chlorobenzene
108-90-7

chlorobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
With dinitrogen tetraoxide; N,N,N,N-tetraethylammonium tetrafluoroborate; In sulfolane; at 30 ℃; Yield given. Yields of byproduct given; electrochemical process;
With zeolite H-beta; Nitrogen dioxide; at 150 ℃; Yield given. Yields of byproduct given;
With zeolite FeAl-ZSM-5; Nitrogen dioxide; at 150 ℃; Yield given. Yields of byproduct given;
With silver nitrate; boron trifluoride; In acetonitrile; at 25 ℃; for 10h; Product distribution; competitive nitration benzene, relative rate;
44 % Chromat.
1 % Chromat.
55 % Chromat.
With phosphoric acid; nitric acid; at 25 ℃; Product distribution; var. conc. of H3PO4;
With N-nitro-2,4,6-trimethylpyridinium tetrafluoroborate; In nitromethane; at 25 ℃; Rate constant; competitive nitration with benzene;
With methyl nitrate; methane; at 37.6 ℃; Product distribution; Irradiation; gas-phase nitration by radiolytically formed MeO(1+)(H)NO2;
With nitrosulphuric acid; sulfuric acid; sulfur trioxide; water; at 9.9 ℃; for 0.666667h; Product distribution; fluorobenzene, var. composition of nitrating acid;
With sulfuric acid; nitric acid; at 10 - 75 ℃; Product distribution; further reagent concentration;
With nitro acetate; H-ZSM-11; In hexane; at 30 ℃; Product distribution; different catalysts, reagents, temperatures;
With Nitrogen dioxide; ozone; In dichloromethane; at 0 ℃; Product distribution; Mechanism; var. solvents; also in the presence of pyridine, HNO3, and MeSO3H, other arenes;
With oxygen; nitrogen(II) oxide; In dichloromethane; at 0 ℃; for 10h; Product distribution; nitration of toluene and chlorobenzene with ternary system NO-NO2-O2; comparison with nitration with other nitrating systems; possible mechanism;
With dinitrogen tetraoxide; In liquid sulphur dioxide; at -30 ℃; Product distribution; other monosubstituted benzenes and heteroaromatic compounds;
With oxygen; Nitrogen dioxide; iron(III)-acetylacetonate; In 1,2-dichloro-ethane; at 0 ℃; relative reaction rate;
With zeolite ZSM-5-60; Nitrogen dioxide; at 250 ℃; Yield given. Yields of byproduct given;
With pyridine; oxygen; Nitrogen dioxide; iron(III)-acetylacetonate; In 1,2-dichloro-ethane; at 0 ℃;
With zeolite Hβ; nitric acid; trifluoroacetic anhydride; at -10 ℃; for 2h; Further Variations:; Reagents; Product distribution;
15 % Chromat.
1 % Chromat.
84 % Chromat.
With NH4β zeolite; oxygen; dinitrogen tetraoxide; In 1,2-dichloro-ethane; at 0 ℃; for 50h; Further Variations:; Reagents; Time; Product distribution;
With 3 A molecular sieve; oxygen; Nitrogen dioxide; HZSM-5; at 20 ℃; for 22h; Title compound not separated from byproducts;
With nitric acid; In water; at 65 ℃; for 0.166667h;
With nitric acid; 1-(n-butyl)-3-methylimidazolium triflate; at 130 ℃; for 108h;
With Broensted acidic ionic liquid; nitric acid; at 80 ℃; for 12h;
With air; Nitrogen dioxide; at -15 - 20 ℃; for 66.5h;
With nitric acid; acetic anhydride; In tetrachloromethane; Reagent/catalyst; Temperature; Catalytic behavior;
With Nitrogen dioxide; at 20 ℃; for 11h; under 3750.38 Torr; Overall yield = 35 %; Overall yield = 0.49 g;
0.16 g
0.02 g
0.31 g
With nitrogen(II) oxide; In dichloromethane; at 50 ℃; for 15h; under 5625.56 Torr; Overall yield = 63 %;
With nitrogen dioxide; oxygen; acetic anhydride; at 35 ℃; under 3750.38 Torr; Pressure; Temperature; Reagent/catalyst; Autoclave;
chlorobenzene
108-90-7

chlorobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-chloro-2,6-dinitrophenol
88-87-9

4-chloro-2,6-dinitrophenol

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
With oxygen; Nitrogen dioxide; iron(III)-acetylacetonate; In 1,2-dichloro-ethane; at 0 ℃; for 36h; Yield given. Yields of byproduct given;
nitromethane
75-52-5

nitromethane

chlorobenzene
108-90-7

chlorobenzene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
Conditions Yield
at 25 ℃;
hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

<i>N</i>-(3-nitro-phenyl)-<i>N</i>'-(4-nitro-phenyl)-triazene
109369-58-6

N-(3-nitro-phenyl)-N'-(4-nitro-phenyl)-triazene

3-Nitrochlorobenzene
121-73-3

3-Nitrochlorobenzene

4-nitro-aniline
100-01-6,104810-17-5

4-nitro-aniline

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

3-nitro-aniline
99-09-2

3-nitro-aniline

Conditions
Conditions Yield
at 100 ℃; im geschlossenen Rohr; Produkt 5: Stickstoff;

Global suppliers and manufacturers

Global( 70) Suppliers
  • Company Name
  • Business Type
  • Contact Tel
  • Emails
  • Main Products
  • Country
  • Simagchem Corporation
  • Business Type:Manufacturers
  • Contact Tel:+86-592-2680277
  • Emails:sale@simagchem.com
  • Main Products:110
  • Country:China (Mainland)
  • Amadis Chemical Co., Ltd.
  • Business Type:Lab/Research institutions
  • Contact Tel:86-571-89925085
  • Emails:sales@amadischem.com
  • Main Products:29
  • Country:China (Mainland)
  • Chemwill Asia Co., Ltd.
  • Business Type:Manufacturers
  • Contact Tel:021-51086038
  • Emails:sales@chemwill.com
  • Main Products:56
  • Country:China (Mainland)
  • Afine Chemicals Limited
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-571-85134551
  • Emails:info@afinechem.com
  • Main Products:92
  • Country:China (Mainland)
  • Kono Chem Co.,Ltd
  • Business Type:Other
  • Contact Tel:86-29-86107037-8015
  • Emails:info@konochemical.com
  • Main Products:82
  • Country:China (Mainland)
  • Hangzhou Dingyan Chem Co., Ltd
  • Business Type:Manufacturers
  • Contact Tel:86-571-86465881,86-571-87157530,86-571-88025800
  • Emails:sales@dingyanchem.com
  • Main Products:95
  • Country:China (Mainland)
close
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 121-73-3
Post Buying Request Now
close
Remarks: The blank with*must be completed