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You Searched For:

2-(3-Piperidinyl)ethyl+cyclopentanecarboxylate+hydrochloride


31,092  results were found

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Supplier:  Matrix Scientific
Description:   2-(4-Piperidinyl)benzoxazole

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 034365-500MG , MDL Number: MFCD11506601
Supplier:  Spectrum Chemicals
Description:   1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride, purity: 98 %, CAS number: 25952-53-8, Molecular Formula: C8H17N3.HCl, Molecular weight: 191.71, Form: Solid, synonyms: monohydrochloride, EDAP, size: 5 g
MSDS SDS
Supplier:  THERMO FISHER SCIENTIFIC CHEMICALS
Description:   (1S,3R)-N-Boc-1-aminocyclopentane-3-carboxylic acid 95%, 98% ee
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 041036-500MG , MDL Number: MFCD12028487
Supplier:  Chem Impex International
Description:   A carbodiimide coupling reagent that generates a urea by-product which can be easily removed from the reaction media by extraction with water

Supplier:  TCI America
Description:   Mitoxantrone dihydrochloride ≥97.0% (by HPLC)
New Product

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 011429-500MG , MDL Number: MFCD00801011
Supplier:  AMBEED, INC
Description:   4-(2-((2-(Benzo[b]thiophen-3-yl)-9-isopropyl-9H-purin-6-yl)amino)ethyl)phenol, Purity: 98+%, CAS Number: 1227633-49-9, Appearance: White to off-white powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8 deg C, Size: 1mg
Supplier:  Matrix Scientific
Description:   MF=C18H25Cln2O2S MW=368.93 ,250Mg
Supplier:  THERMO FISHER SCIENTIFIC CHEMICALS
Description:   3-Oxocyclopentanecarboxylic acid 97%
Supplier:  Matrix Scientific
Description:   MF=C18H25Cln2O2S MW=368.93 ,250Mg
Supplier:  Matrix Scientific
Description:   MF=C11H14Cln3Os MW=271.77 ,250Mg
Supplier:  Matrix Scientific
Description:   MF=C16H22Cln5 MW=319.84 250Mg
Supplier:  Invitrogen
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.
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 026684-500MG , MDL Number: MFCD09997685
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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 at 1-800-932-5000.
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 Regulatory_Affairs@vwr.com
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1,761 - 1,776  of 31,092