You Searched For: Fmoc-D-3-Abu-OH


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Supplier: Bachem Americas
Description: Sequence: Fmoc-Abu-OH

Supplier: Ambeed
Description: Fmoc-Abu-OH 98%

New Product

Catalog Number: (B-4205.1000BA)
Supplier: Bachem Americas
Description: Sequence: Fmoc-4-(7-hydroxy-4-coumarinyl)-Abu-OH
Synonym(s): Fmoc-(7-hydroxycoumarin-4-yl)-ethyl-Gly-OH#Fmoc-(umbellifer-4-yl)-ethyl-Gly-OH


Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 041565-1G , MDL Number: MFCD00270336

Catalog Number: (101852-384)
Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 041589-5G , MDL Number: MFCD00080268


Catalog Number: (F-4040.0001BA)
Supplier: Bachem Americas
Description: Sequence: (S)-2-(Fmoc-amino)-4-neopentyloxysulfonyl-butyric acid


Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Abu-OH

Supplier: Ambeed
Description: Fmoc-D-Abu-OH, Purity: 97%, CAS Number: 170642-27-0, Appearance: White to off-white solid, Storage: Sealed in dry, Room Temperature, Size: 1G

Supplier: Bachem Americas
Description: Sequence: Fmoc-γ-Abu-OH

Supplier: Thermo Scientific Chemicals
Description: (R)-2-(Fmoc-amino)butyric acid, Purity: 98%, CAS Number: 170642-27-0, Molecular Formula: C19H19NO4, Synonym: Fmoc-D-Abu-OH, Size: 1G

SDS

Supplier: Ambeed
Description: (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid, Purity: 98%, CAS Number: 201864-71-3, Appearance: White to Yellow Solid, Storage: Sealed in dry, 2-8C, Size: 1G

Supplier: TCI America
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-aminobutyric Acid, Purity: >98.0%(HPLC)(T), CAS Number: 116821-47-7, Molecular Formula: C19H19NO4, MW: 325.36, Synonym: N-Fmoc-4-aminobutyric Acid, Fmoc-GABA-OH, Form: Crystal- Powder, Size: 5G

SDS

Supplier: Thermo Scientific Chemicals
Description: 4-(Fmoc-amino)butyric acid, 95%
Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 041580-5G , MDL Number: MFCD00144889

Supplier: Ambeed
Description: Fmoc-GABA-OH 97%

Supplier: Bachem Americas
Description: Protected derivative of L-azidohomoalanine (Aha), a Met isostere. This building block for 'click chemistry' additionally creates a specific cleavage site in peptides, Aha-containing sequences can be cleaved under mild conditions in the presence of phosphines or dithiols via formation of homoserine lactone.

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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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