You Searched For: 2-(2,3-Dichlorophenyl)thioacetamide


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Supplier: Apollo Scientific
Description: 2-(4,5-Dichloro-1H-imidazol-1-yl)ethanethioamide

Supplier: Honeywell Chemicals
Description: Thioacetamide ACS reagent for the precipitation of heavy metals.

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Supplier: MP Biomedicals
Description: Thioacetamide is a hepatotoxin and a carcinogen. Thioacetamide is also an additive in enantioselective reduction of β-keto esters with immobilized bakers yeast.

Catalog Number: (BOSSBS-11850R)
Supplier: Bioss
Description: GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel ∫-sheet, a parallel ∫-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel ∫-sheet, a parallel ∫-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with ©-GCS and ending with GSS. In an ATP-dependent reaction, GSS produces Glutathione from ©-glutamylcysteine and glycine precursors. Partial hepatectomy, diethyl maleate, buthionine sulfoximine, tert-butylhaydroquinone and thioacetamide increase the ex-pression of GSS, which causes an increase in Glutathione levels. An inherited autosomal recessive disorder, 5-oxoprolinuria (pyroglutamic aciduria), is caused by GSS deficiencies, which leads to central nervous system damage, hemolytic anemia, metabolic acidosis and urinary excretion of 5-oxoproline. A missense mutation in the gene encoding GSS leads to a GSS deficiency restricted to erythrocytes, which causes only hemolytic anemia.-GCS and ending with GSS.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-11850R-HRP)
Supplier: Bioss
Description: GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel ∫-sheet, a parallel ∫-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with GSS (Glutathione synthetase) is a 474 amino acid protein encoded by the gene located at human chromosome 20q11.2. GSS consists of three loops projecting from an antiparallel ∫-sheet, a parallel ∫-sheet and a lid of anti-parallel sheets, which provide access to the ATP-binding site. Although Southern blot and gene analysis suggest that GSS may be the only member of a unique family, the crystal structure indicates that GSS belongs to the ATP-GRASP superfamily. GSS is expressed in hemocytes and nucleated cells, including the brain. GSS occurs as a homodimer. There are two steps in the production of Glutathione, begining with ©-GCS and ending with GSS. In an ATP-dependent reaction, GSS produces Glutathione from ©-glutamylcysteine and glycine precursors. Partial hepatectomy, diethyl maleate, buthionine sulfoximine, tert-butylhaydroquinone and thioacetamide increase the ex-pression of GSS, which causes an increase in Glutathione levels. An inherited autosomal recessive disorder, 5-oxoprolinuria (pyroglutamic aciduria), is caused by GSS deficiencies, which leads to central nervous system damage, hemolytic anemia, metabolic acidosis and urinary excretion of 5-oxoproline. A missense mutation in the gene encoding GSS leads to a GSS deficiency restricted to erythrocytes, which causes only hemolytic anemia.-GCS and ending with GSS.
UOM: 1 * 100 µl


Supplier: Merck
Description: 3,5-Dichlorophenyl isocyanate for synthesis
Catalog Number: (45432-250MG)
Supplier: Merck
Description: Dichlofenthion(O-2,4-dichlorophenyl-O,O-diethyl phosphorothioate), Supelco®
UOM: 1 * 250 mg


Catalog Number: (04718-50MG)
Supplier: Merck
Description: Organic Standard, {2-[(2,6-Dichlorophenyl)amino]phenyl}methanol
UOM: 1 * 50 mg


Supplier: Apollo Scientific
Description: 5-(2,5-Dichlorophenyl)-2-furaldehyde

Catalog Number: (APOSOR5-250MG)
Supplier: Apollo Scientific
Description: 5-(3,4-Dichlorophenyl)isoxazole
UOM: 1 * 250 mg


Catalog Number: (APOSOR346288-1G)
Supplier: Apollo Scientific
Description: 2-(3,5-Dichlorophenyl)acetonitrile
UOM: 1 * 1 g


Supplier: Apollo Scientific
Description: (3,4-Dichlorophenyl)acetonitrile

Supplier: Thermo Scientific
Description: 2,6-Dichlorophenyl isocyanate ≥98%
Supplier: Apollo Scientific
Description: 2-(3,5-Dichlorophenyl)hydrazinecarbothioamide, Technical Grade

Catalog Number: (APOSOR13643-100G)
Supplier: Apollo Scientific
Description: 1-(2,4-Dichlorophenyl)-2-(1-imidazolyl)ethanol
UOM: 1 * 100 g


Catalog Number: (APOSOR51794-5G)
Supplier: Apollo Scientific
Description: (3,5-Dichlorophenyl)acetic acid
UOM: 1 * 5 g


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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