You Searched For: Phosphorus+pentoxide+-+methanesulphonic+acid


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Supplier: Apollo Scientific
Description: Phosphorus(V) bromide 95%

Supplier: Thermo Fisher Scientific
Description: Methanesulphonic anhydride ≥98%
Catalog Number: (APOSPC430262-1G)
Supplier: Apollo Scientific
Description: trans-3-Fluoro-tetrahydro-2H-pyran-4-yl methanesulphonate racemate
UOM: 1 * 1 g


Supplier: Apollo Scientific
Description: Pentafluorophenyl-(3-chlorophenyl)methanesulphonate

Supplier: Apollo Scientific
Description: Tetrahydro-2H-pyran-4-yl methanesulphonate

Catalog Number: (APOSOR302751-1G)
Supplier: Apollo Scientific
Description: Oxetan-3-yl methanesulphonate
UOM: 1 * 1 g


Supplier: Thermo Fisher Scientific
Description: Copper phosphorus shot
Supplier: Thermo Fisher Scientific
Description: Vanadium(V) oxide ≥99.99% (metals basis)
Supplier: Apollo Scientific
Description: 2-(Aminomethyl)-1H-indole methanesulphonate 95%

Catalog Number: (ENZOENZ52253)
Supplier: ENZO LIFE SCIENCES
Description: Neuronal detection
UOM: 1 * 10 mg


Supplier: Thermo Fisher Scientific
Description: Arsenic (V) oxide ≥99.9% (metals basis)
Supplier: Thermo Fisher Scientific
Description: Phosphorus(V) bromide 95%
Catalog Number: (46693.03)
Supplier: Thermo Fisher Scientific
Description: Polyethylene glycol monomethyl ether methanesulphonate, M.W. 13,000
UOM: 1 * 1 g

Catalog Number: (BTIUBNUM1173-50)
Supplier: Biotium
Description: The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
UOM: 1 * 50 µl


Catalog Number: (BTIUBNUM1174-50)
Supplier: Biotium
Description: The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
UOM: 1 * 50 µl


Catalog Number: (BTIUBNUM1175-50)
Supplier: Biotium
Description: The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
UOM: 1 * 50 µl


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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
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
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The original product is no longer available. The replacement shown is available.
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