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ALADDIN SCIENTIFIC
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ALADDIN SCIENTIFIC
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Acetyl-2-methylpyridine ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
3-Amino-5-chlorophenol ≥97%
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ALADDIN SCIENTIFIC
Description:
2-Acetamido-5-nitropyridine ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Acetyl-5-methylpyridine ≥96%
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-1-cyclopentene-1-carbonitrile ≥98%
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ALADDIN SCIENTIFIC
Description:
2-Amino-N-methylacetamide ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
ADL5859 is a δ-opioid receptor agonist with Ki of 0.8 nM, selectivity against opioid receptor κ, μ, and weak inhibitory activity at the hERG channel.A selective receptor agonist for the δ-opioid receptor
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-4,6-dimethylpyridine ≥98%
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ALADDIN SCIENTIFIC
Description:
4-Amino-3-chlorophenol hydrochloride ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-3-bromo-5,6-dimethylpyridine ≥98%
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Amino-3,5-difluorobenzonitrile ≥97%
Supplier:
ALADDIN SCIENTIFIC
Description:
A-803467 inhibits spontaneous and evoked action potentials in sensory neurons. It exhibits antinociceptive effects.A-803467 decreases the firing in spinal dorsal horn neurons in vivo.The small molecule A-803467 is a potent and selective Nav1.8 sodium channel blocker. Nav1.8 is a tetrodotoxin-resistant (TTX-R) sodium channel that contributes to pain sensation by transmitting pain stimuli in peripheral sensory neurons; blockage of this channel by A-803467 reduces pain with varying effectiveness in a number of different models.A-803467 has been used to further understand the role of Nav1.8 in transmitting pain stimuli and also can be used as an analgesic
Catalog Number:
(ALA151024-25G)
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Acetamidobenzaldehyde ≥98% (by GC)
Supplier:
ALADDIN SCIENTIFIC
Description:
Azide/azido functionalized polyethylene glycol (N3-PEG-X) is a bifunctional PEG derivative that can be used to modify proteins, peptides and other materials. Azide group can react with alkyne in aqueous solution catalyzed by copper. It can also be reduced into amine group easily while another functional group can be react with other molecules or functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Acryloylmorpholine is an acrylate monomer widely used as a crosslinking agent in the polymer industry. It is used to form three-dimensional polymer networks to enhance the mechanical strength, stability, and durability of materials. The morpholine moiety in acryloylmorpholine imparts hydrophilicity to the molecule facilitating its applications in the field of adhesives, biocompatible coatings, and drug delivery systems. It is also used as a reactive monomer to synthesize hydrogels for drug delivery, photocurable materials for 3D bioprinting and display devices. Purpose
4-Acryloylmorpholine can be used as a monomer:To synthesize multiblock copolymers via RAFT polymerization. These functional block copolymers find application in the fields of medicine, energy, and nanotechnology.To prepare organogel electrode frame via photopolymerization and cross-linking. This can be used to fabricate triboelectric nanogenerators with excellent transparency, stretchability, and interface adhesion.For printing thermoplastic 3D tissue scaffolds. ACMO′s water solubility,and remarkably low viscosity, combined with surface oxygen inhibition, promoteswift liquid flow during high-speed open-air printing.
Supplier:
ALADDIN SCIENTIFIC
Description:
2-(1-Aminocyclohexyl)acetic acid hydrochloride ≥95%
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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
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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