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Cas:76-01-7
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Cas:76-01-7
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:76-01-7
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiry76-01-7 PENTACHLOROETHANE Application:76-01-7 PENTACHLOROETHANE
76-01-7 PENTACHLOROETHANEAppearance:colourless liquid with a camphor-like smell Storage:2-8°C Package:As your request Application:76-01-7 Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport)
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:76-01-7
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryTech Data Relevant 1.Certificate Of Analysis (COA) 2..Material Safety Data Sheet (MSDS) 3.Technical Data Sheet(TDS) 4.Route of synthesis (ROS) 5.Nuclear Magnetic Resonance(NMR) 6.Method of Analysis(MOA) Our Service 1. Before Shipmen
Cas:76-01-7
Min.Order:100 Kilogram
Negotiable
Type:Trading Company
inquiryProduct name : Pentachloroethane Chemical Name : Pentachloroethane Molecular Formula : CHCL2CCL3 Molecular Weight : 202.29 Appearance : Colo
Cas:76-01-7
Min.Order:200 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryAt Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
Pentachloroethane Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
76-01-7 PENTACHLOROETHANE Application:76-01-7
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
Conditions | Yield |
---|---|
With chlorine at 10 - 20℃; for 11h; Inert atmosphere; Cooling with ice; | 99% |
With tetrachloromethane; chlorine monoxide at -20℃; | |
With chlorine at 0℃; im Sonnenlicht; |
N,N-Dichlorobenzenesulfonamide
Trichloroethylene
A
pentachloroethane
B
N-(2,2,2-trichloroethylidene)benzenesulfonamide
Conditions | Yield |
---|---|
at 85 - 90℃; Product distribution; Other temperatures, UV irradiation, presence of azoisobutyronitrile or benzoyl peroxide.; | A n/a B 97% |
at 85 - 90℃; Other temperatures, UV irradiation, presence of azoisobutyronitrile or benzoyl peroxide.; | A n/a B 97% |
1,1,1-trichloroethane
A
1,1,1,2-tetrachoroethane
B
1,1-Dichloroethylene
C
pentachloroethane
Conditions | Yield |
---|---|
With chlorine at 25℃; Irradiation; | A 92.5% B 2.4% C 5.1% |
With chlorine at 25℃; Irradiation; | A 89.9% B 4.7% C 5.3% |
1,1-dichloroethane
A
1,1,1-trichloroethane
B
1,1,2-trichloroethane
C
pentachloroethane
Conditions | Yield |
---|---|
With chlorine at 200℃; for 0.05h; Mechanism; Irradiation; other temperature; | A 83.1% B 6.3% C 0.5% |
With chlorine at 200℃; for 0.05h; Irradiation; | A 83.1% B 6.3% C 0.5% |
N,N-Dichlorobenzenesulfonamide
Trichloroethylene
A
benzenesulfonamide
B
pentachloroethane
C
N-(2,2,2-trichloroethylidene)benzenesulfonamide
D
N-(2,2,2-trichloro-1-benzenesulfonamidoethyl)benzenesulfonamide
Conditions | Yield |
---|---|
With tin(IV) chloride at 20 - 22℃; for 1080h; Product distribution; other time, temperature, Lewis acid (AlCl3); | A n/a B n/a C n/a D 81% |
1,1,2,2-tetrachloroethane
A
1,1,2,2-tetrachloroethylene
B
Trichloroethylene
C
pentachloroethane
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen at 379.84℃; | A 20.8% B 64.3% C 6.1% |
Trichloroethylene
N,N-dichloro-benzamide
A
pentachloroethane
B
N-(2,2,2-trichloro-1-hydroxyethyl)benzamide
C
benzamide
D
N-(dichloroacetyl)benzamide
Conditions | Yield |
---|---|
With air for 11h; Heating; | A n/a B n/a C n/a D 37% |
Trichloroethylene
N,N-dichlorotrifluoromethylsulfonamide
A
pentachloroethane
C
1,1,1-trifluoro-N-(2,2,2-trichloroethylidene)methanesulfonamide
Conditions | Yield |
---|---|
at 20℃; for 25h; | A n/a B n/a C 35% |
(2,2-dichloro-vinyl)-trimethyl-silane
A
Trichloroethylene
B
pentachloroethane
Conditions | Yield |
---|---|
With chlorine for 3h; Further byproducts given; | A 5% B 2% C 30% D 33% |
Trichloroethylene
N,N-dichloro-benzamide
A
pentachloroethane
B
N-(2,2,2-trichloro-1-hydroxyethyl)benzamide
C
1,1,1-trichloro-2,2-dibenzamidoethane
D
benzamide
Conditions | Yield |
---|---|
at 85 - 90℃; for 10h; | A n/a B n/a C 28% D n/a |
Trichloroethylene
N,N-dichloro-acetamide
A
acetamide
B
pentachloroethane
C
N-(2,2,2-trichloro-1-hydroxyethyl)-acetamide
D
2,2,2-trichloro-1,1-diacetamidoethane
Conditions | Yield |
---|---|
at 85 - 90℃; for 10h; | A n/a B n/a C n/a D 17% |
Conditions | Yield |
---|---|
With chlorine at 379.84℃; Reagent/catalyst; Temperature; | A 8.1% B 11.2% |
Trichloroethylene
N,N-dichloro-4-chlorobenzenesulfonamide
A
4-Chlorobenzenesulfonamide
B
pentachloroethane
C
N-(2,2,2-trichloroethylidene)-4-chlorobenzenesulfonamide
D
N-(2,2,2-trichloro-1-p-chlorobenzenesulfonamidoethyl)-p-chlorobenzenesulfonamide
Conditions | Yield |
---|---|
With tin(IV) chloride at 20 - 22℃; for 720h; Product distribution; other time, temperature, Lewis acid (AlCl3); | A n/a B n/a C n/a D 7.1% |
N,N-dichloro-p-toluenesulfonamide
Trichloroethylene
A
N-(2,2,2-trichloroethyliden)-p-toluenesulfonamide
B
pentachloroethane
C
N-(2,2,2-trichloro-1-p-toluenesulfonamidoethyl)-p-toluenesulfonamide
D
toluene-4-sulfonamide
Conditions | Yield |
---|---|
With tin(IV) chloride at 20 - 22℃; for 1560h; Product distribution; other time, temperature, Lewis acid (AlCl3); | A n/a B n/a C 2.7% D n/a |
Conditions | Yield |
---|---|
Einw. dunkler elektrischer Entladungen; |
diethyl ether
hexachloroethane
ethylmagnesium bromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
diethyl ether
hexachloroethane
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
beim Chlorieren; |
Conditions | Yield |
---|---|
Einw. dunkler elektrischer Entladungen; | |
Brennen eines Lichtbogens (?); | |
In water at 25℃; Kinetics; sonolysis; sonication; |
chloroform
A
tetrachloromethane
B
1,1,2,2-tetrachloroethylene
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
beim Durchgang des elektrischen Lichtbogens; weitere Produkten: Hexachloraethan, Hexachlorbenzol, HCl und Kohle; |
1,1,1-trichloroethane
A
1,1,1,2-tetrachoroethane
B
pentachloroethane
C
hexachloroethane
Conditions | Yield |
---|---|
Chlorierung im Sonnenlicht; |
Conditions | Yield |
---|---|
With chlorine at 1001℃; |
Trichloroethylene
A
pentachloroethane
B
1,1,2,2-tetrachloro-1-nitroethane
Conditions | Yield |
---|---|
With nitrosylchloride |
Conditions | Yield |
---|---|
With phosphorus pentachloride |
Conditions | Yield |
---|---|
With phosphorus pentachloride | |
With aluminium trichloride |
Conditions | Yield |
---|---|
beim Chlorieren; |
diethyl ether
hexachloroethane
para-methylphenylmagnesium bromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
diethyl ether
hexachloroethane
1-naphthylmagnesiumbromide
A
1,1,2,2-tetrachloroethylene
B
1,1,1,2-tetrachoroethane
C
pentachloroethane
D
1,1,2,2-tetrachloroethane
Conditions | Yield |
---|---|
With pumice stone at 700℃; | |
With chlorine Irradiation.UV-Licht; | |
With hydrogenchloride; oxygen at 349.84℃; Reagent/catalyst; Temperature; |
Conditions | Yield |
---|---|
With methyl diethylphosphinate at 150℃; for 10h; | 75% |
With chlorine at 379.84℃; Gas phase; chemoselective reaction; | 33.8% |
With nickel dichloride at 330℃; |
pentachloroethane
Conditions | Yield |
---|---|
In chloroform at 20℃; for 0.833333h; | 46% |
Conditions | Yield |
---|---|
With iodobenzene; tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide for 5.6h; Ambient temperature; electrolysis; Cd-coated cathode, Mg anode; | 45% |
Conditions | Yield |
---|---|
With hexacarbonyl molybdenum at 140℃; for 3h; further reagent Fe(CO)5; | A 42% B 23% |
With iron pentacarbonyl at 140℃; for 3h; further reagent Mo(CO)6; | A 27% B 23% |
Conditions | Yield |
---|---|
With 2-hydroxy-2-phenylacetophenone; iron(III) chloride In acetonitrile at 130℃; | 40% |
Conditions | Yield |
---|---|
Irradiation (UV/VIS); with Cl2 sensibilized photochemical oxidn., 80 to 100°C; | A 20% B n/a |
piperidine
tetrachloromethane
pentachloroethane
1,1,2,2-tetrachloroethylene
Conditions | Yield |
---|---|
at 20℃; |
Conditions | Yield |
---|---|
With aluminium trichloride at 40℃; 1,1,2,3,4-pentachloro-butane, solid form; | |
With aluminium trichloride at 40℃; 1,1,2,3,4-pentachloro-butane, liquid form; |
Conditions | Yield |
---|---|
With aluminium trichloride at 40℃; |
Conditions | Yield |
---|---|
With aluminium trichloride |