You Searched For: Ethyl+formate


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Supplier: Merck
Description: Ethyl formate for synthesis
Catalog Number: (88554-5ML-F)
Supplier: Merck
Description: Ethyl formate, Supelco®
UOM: 1 * 5 mL


Supplier: Thermo Scientific
Description: Ethyl formate ≥97%
Supplier: Thermo Scientific
Description: Ethyl formate 98+%, pure
Supplier: Apollo Scientific
Description: Ethyl-2-naphthoyl formate, Technical Grade

Supplier: Apollo Scientific
Description: Ethyl-4-bromobenzoyl formate 95%

Catalog Number: (APOSOR32664-1G)
Supplier: Apollo Scientific
Description: Ethyl (benzylcarbamoyl)formate, tech
UOM: 1 * 1 g


Supplier: Merck
Description: Triethyl phosphonoformiate for synthesis, Sigma-Aldrich®
Catalog Number: (1265606.)
Supplier: USP
Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 3 Ampoul


Supplier: ENZO LIFE SCIENCES AG
Description: A novel, selective inhibitor of receptor-mediated calcium entry. It inhibits receptor-mediated calcium entry in stimulated platelets (IC50=8-12µM) neutrophils and endothelial cells at concentrations which do not affect internal Ca²⁺ release. Note, in some cells SK&F 96365 can activate a novel Ca²⁺ entry pathway. Blocks TRPC3 and TRPC6 activation. Inhibits the histamine-induced formation of nitric oxide in human endothelial cells.

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Catalog Number: (429241000.)
Supplier: Thermo Scientific
Description: Ethyl formate, extra dry 98+%, AcroSeal®
UOM: 1 * 100 mL

Catalog Number: (ROTH3574.1)
Supplier: Roth Carl
Description: Ethyl formate
UOM: 1 * 1 L

Market Source Item This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLE19063440-500G)
Supplier: Molekula
Description: Triethyl phosphonoformiate
UOM: 1 * 500 g

Market Source Item This is a MarketSource item. Additional charges may apply

Catalog Number: (PIER23030)
Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce N-Ethylmaleimide (NEM) is a small compound that forms stable, covalent thioether bonds with sulfhydryls (e.g., reduced cysteines), enabling them to be permanently blocked to prevent disulfide bond formation.
UOM: 1 * 25 g

Catalog Number: (PIERA35391)
Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
UOM: 1 * 10 mg


Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
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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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