Diethyl adipate has an antifertility effects.

Amino-PEG5-CH2CO2H is a PEG derivative containing an amino group with a terminal carboxylic acid. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

Ricinoleic acid is a fatty acid.

Alfadolone is an anesthetic derivative of pregnanedione.

gamma-Tocotrienol is one of the four types of tocotrienol, a type of vitamin E. gamma-Tocotrienol is a radioprotector, antioxidant, and shows antitumor and antihypertensive effects in vivo.

Proxan-sodium is a biochemical.

Iprovalicarb is a fungicide specific to oomycetes.

Tyrphostin AG957 is a tyrosine kinase inhibitor, selectively inhibiting human p210 tyrosine kinase activity.

Bacitracin is an antibiotic. It has been shown to disrupt gram positive bacteria by interfering with cell wall and peptidoglycan synthesis.

Fenaminosulf is an active ingredient in several commercial fungicides, and reported to be mutagenic in Salmonella typhimurium.

N-Boc-PEG5-alcohol is a PEG derivative containing a hydroxyl group and Boc-protected amino group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Ald-Ph-PEG3-amine TFA salt is a PEG Linker

4-Chlorophenylurea is a novel orally bioavailable factor Xa inhibitor.

Candicidin is a mixture of antifungal heptaene macrolides from Streptomyces griseus or Actinomyces levoris used topically in candidiasis. The antibiotic complex is composed of candicidins A, B, C, and D, of which D is the major component.

Benzathine is a diamine used as a component in some medications including benzathine phenoxymethylpenicillin and benzathine benzylpenicillin. It stabilises penicillin and prolongs its sojourn when injected into tissues.

Amphomycin inhibits mannosylphosphoryldolichol synthesis by forming a complex with dolichylmonophosphate.

Dibenzyl sebacate is a biochemical.

Bromo-PEG5-azide is a PEG derivative containing a bromide group and a terminal azide. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage.

Azido-PEG5-succinimidyl carbonate is a PEG Linker.

Diphenylcarbazide is used for determination of chromium.

Fmoc-PEG5-NHS ester is a PEG derivative containing an Fmoc-protected amine and an NHS ester. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.

Amlodipine besilate impurity F, also known as Amlodipine Dimethyl Ester, is a biochemical.

Amlodipine besilate impurity E is a biochemical.

Metaflumizone is an insecticide

Azido-PEG4-Amido-Tris, also known as Azido-PEG4-Amido-tri-(carboxyethoxymethyl)-methane, is a multi-arm PEG containing an azide group and three hydroxyl groups. The azide group enables Click Chemistry. The indicated molecular weight of the multi-arm PEG is the sum of the molecular weights of all the arms. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.

2-(Azido-PEG2-amido)-1,3-propandiol is a multi-arm PEG with azide or hydroxyl at the terminal of all arms. The azide group enables Click Chemistry. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.

Azido-PEG4-Amido-tri-(carboxyethoxymethyl)-methane is a branched PEG derivative with a terminal azide group and three terminal carboxylic acids. The azide group enables PEGylation via Click Chemistry. The terminal carboxylic acids can be reacted with primary amino groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.

Propargyl-PEG5-beta-D-glucose is a Click Chemistry-ready crosslinker containing a propargyl group and beta-D-glucose. The propargyl groups can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield stable triazole linkages. D-glucose increases solubility in aqueous media and increases the selectivity of the PEGylation reaction.

Propargyl-PEG5-tetra-Ac-beta-D-galactose is a Click Chemistry-ready crosslinker containing a propargyl group and beta-D-galactose. The propargyl groups can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield stable triazole linkages. D-galactose increases solubility in aqueous media and a the selectivity of the PEGylation reaction.

R(+)-6-Bromo-APB HBr is a potent D1 Dopamine receptor agonist.