Others

Itraconazole impurity 4 is an impurity of Itraconazole.

3,6-Dichloro-2-hydroxybenzoic acid-¹³C₆ is the ¹³C labeled 3,6-Dichloro-2-hydroxybenzoic acid.

4-Iodobenzylamine hydrochloride ((4-Iodophenyl)methanamine hydrochloride) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA).

4-Arm PEG5000-NH2 (GMP) (4-Arm PEG5000-amine (GMP)) is 4-Arm PEG-NH2 (HY-W1048843A) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. 4-Arm PEG5000-NH2 is a multi-arm PEG derivative with amine groups at each end of four arms attached to a pentaerythritol core. The reactive primary amine or NH2 groups can react rapidly with activated carboxylic acids such as NHS esters to form stable amide bonds.

4-Arm PEG5000-NH2 (GMP Like) (4-Arm PEG5000-amine (GMP Like)) is 4-Arm PEG-NH2 (HY-W1048843A) produced by using GMP like guidelines. GMP like small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. 4-Arm PEG5000-NH2 is a multi-arm PEG derivative with amine groups at each end of four arms attached to a pentaerythritol core. The reactive primary amine or NH2 groups can react rapidly with activated carboxylic acids such as NHS esters to form stable amide bonds.

2,3,5-Trichloro-4-pyridinol can be used as a herbicide for direct-seeded and flooded rice.

N3-PEG2-CH2CO2-NHS is a PEG derivative containing an azide group and an NHS ester. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.

(R)-DPPE-mPEG(2000) is a lipid that can be used to prepare lipid nanoparticles (LNPs) for drug delivery.

Benzyltrimethylsilane-d2 (α-Trimethylsilyltoluene-d2) is the deuterium labeled Benzyltrimethylsilane (HY-W585956).

Dimethylpropiothetin hydrochloride (Standard) (s,s-Dimethyl-β-propionic acid thetine (Standard)) is the analytical standard of Dimethylpropiothetin hydrochloride (HY-W105506). This product is intended for research and analytical applications. Dimethylpropiothetin hydrochloride is a dimethylsulfide precursor. Dimethylpropiothetin hydrochloride can be isolated from the marine coccolithophore Hymenomonas carterae. Dimethylpropiothetin hydrochloride participates in the maintenance of cellular osmotic pressure.

Tenofovir impurity 24 is an impurity of Tenofovir.

(E)-3-(Phenylsulfonyl) acrylic acid is a sulfonyl acrylic acid intermediate that can be used for the preparation of NLRP3 inflammasome inhibitors.

Dibutyltin bis (2-ethylhexanoate) is an orally active metal-based catalyst with cytotoxicity, and exhibits acute oral toxicity in white-footed mice.

Di-n-propyl sulfoxide is an alkyl sulfoxide with no radioprotective activity against lethal x-ray doses in mice.

1,2-Bis (3-hydroxyphenyl) ethane-1,2-dione is a 3,3'-dihydroxybenzil that serves as a starting material for the synthesis of bis-acyloxy-BTP complexing agents.

Copper dihydroxide is a copper group metal hydroxide molecule with significant covalent character, a planar ²B₉ ground-state electronic state, and C_2h symmetry.

Pantoprazole impurity 26 is an impurity of Pantoprazole (HY-17507).

9-Bromo-10-(2-naphthyl)anthracene-d₁₅ is the deuterium labeled 9-Bromo-10-(2-naphthyl)anthracene.

Quasar670 Phosphoramidite is a modified phosphoramidite monomer that can be used for oligonucleotide synthesis and fluorescent in situ hybridization probe synthesis. Oligonucleotide probes synthesized with Quasar670 Phosphoramidite can be used to detect eGFP mRNA in fixed cells; they can target the 26S rRNA D1/D2 region of Hanseniaspora uvarum to enable tracking and detection of this yeast strain.

Spacer-C2 Phosphoramidite is a C2 spacer phosphoramidite modifier for oligonucleotide synthesis that introduces a hydrophobic two-carbon spacer internally or at the 5′ end of an oligonucleotide. Spacer-C2 Phosphoramidite increases the distance between an oligonucleotide and a modifier, thereby reducing interactions between the modifier and the oligonucleotide sequence, and can be used for oligonucleotide modification and labeling research.