Text Search >
trans-4-(4-Fluorobenzoyl)cyclohexane-1-carboxylic+acid
Print…
You Searched For:
153,170 results were found
trans-4-(4-Fluorobenzoyl)cyclohexane-1-carboxylic+acid
Catalog Number:
(101849-532)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040449-500MG , MDL Number: MFCD04035220
Supplier:
AMBEED, INC
Description:
trans-Methyl 4-(hydroxymethyl)cyclohexanecarboxylate, Purity: 97%, CAS Number: 110928-44-4, Appearance: Colorless to Pale-yellow Solid or Liquid, Storage: Inert atmosphere, 2-8C, Size: 100MG
Catalog Number:
(101849-530)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040448-500MG , MDL Number: MFCD03233093
Supplier:
Matrix Scientific
Description:
trans-Methyl 4-(hydroxymethyl)cyclohexanecarboxylate ≥97%
Catalog Number:
(MK235757)
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
For Laboratory,Research,or Manufacturing Use
Catalog Number:
(102848-660)
Supplier:
Matrix Scientific
Description:
cis-3-(4-Fluorobenzoyl)cyclopentane-1-carboxylic acid ≥95%
Catalog Number:
(101929-672)
Supplier:
Matrix Scientific
Description:
MF=C13H14Fno3 MW=251.26 MDL=MFCD03278694 500Mg
Catalog Number:
(PI22360)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce SMCC is a hetero-bifunctional crosslinker that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7–9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5–7.5 to form stable thioether bonds. In aqueous solutions, NHS ester hydrolytic degradation is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group, but will slowly hydrolyze and lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugations with these crosslinkers are usually performed at pH 7.2–7.5, with the NHS ester (amine-targeted) reacted before or simultaneous with the maleimide (sulfhydryl-targeted) reaction.
Catalog Number:
(102836-702)
Supplier:
Matrix Scientific
Description:
2-(4-Fluorobenzoyl)benzoic acid ≥97%
Catalog Number:
(103523-926)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce SMCC is a hetero-bifunctional crosslinker that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7–9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5–7.5 to form stable thioether bonds. In aqueous solutions, NHS ester hydrolytic degradation is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group, but will slowly hydrolyze and lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugations with these crosslinkers are usually performed at pH 7.2–7.5, with the NHS ester (amine-targeted) reacted before or simultaneous with the maleimide (sulfhydryl-targeted) reaction.
Supplier:
AMBEED, INC
Description:
trans-Cyclohexane-1,3-dicarboxylic acid 95%
Supplier:
AMBEED, INC
Description:
1-(4-Fluorobenzoyl)-3-(((6-methoxynaphthalen-2-yl)oxy)methyl)azetidine-3-carboxylic acid, Purity: 98+%, CAS Number: 1078166-57-0, Appearance: Form: solid, Storage: Sealed in dry, Room Temperature, Size: 1g
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 046496-1G , MDL Number: MFCD08443967
Supplier:
AMBEED, INC
Description:
1-tert-Butoxycarbonyl-4-(4-fluorobenzoyl)piperidine 96%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 044109-5G , MDL Number: MFCD00202775
Supplier:
AAT BIOQUEST INC
Description:
SMCC is a non-cleavable and membrane permeable crosslinker with a spacer arm of 8.3 â„«. It contains an amine-reactive succinimidyl ester (SE) and a sulfhydryl-reactive maleimide group. NHS esters react with primary amines at pH 7 to 9 to form stable amide bonds. Maleimides react with sulfhydryl groups at pH 6.5 to 7.5 to form stable thioether bonds. The SE group of SMCC is reacted with lysine residues on the carrier protein, converting them to reactive maleimides. SMCC is a reagent that is widely used for generating stable maleimide-activated carrier proteins that can spontaneously react with sulfhydryls. Alternatively these relatively stable maleimide-activated intermediates may be lyophilized and stored for later conjugation to a hapten.
Inquire for Price
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
 is still displayed and you need assistance, please call us at 1-800-932-5000.
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
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
|
|||||||||
List View
