Chromatography Standards
Ethyl butyrate, ≥99.5% (GC), MilliporeSigma™ Supelco™
Ethyl butyrate belongs to the class of esters and is generally employed as a flavor enhancer in commercial food products.
PESTANAL™ Phosalone, MilliporeSigma™ Supelco™
Phosalone is a commonly used, organophosphate insecticide, which can find applications in agricultural production. It can act effectively on lipid peroxidation and other antioxidant enzymes like superoxide dismutase, catalase and also glutathione peroxidase.
3-Amino-1-propanol, ≥99.5% (GC), MilliporeSigma™ Supelco™
3-Amino-1-propanol is a linear primary alkanolamine.
PESTANAL™ Transfluthrin, MilliporeSigma™ Supelco™
Transfluthrin is a contact, pyrethroid ester insecticide, with repellent activity. Its mode of action involves a knock down effect in insect pests such as moths, cockroaches, flies, whitefly and mosquitoes.
Mettler-Toledo™ Calibration Substance ME 18555, For the calibration of the thermosystem 900, MilliporeSigma™ Supelco™
Benzoic acid is an aromatic acid, which occurs physically as colorless leaflets or white needles.
PESTANAL™ Butocarboxim, MilliporeSigma™ Supelco™
Butocarboxim is a carbamate pesticide commonly used as an insecticide and miticide. The mode of action of butocarboxim involves the inhibition of the enzyme activity of acetylcholinesterase (AChE).
PESTANAL™ MCPA-2-ethylhexyl ester, MilliporeSigma™ Supelco™
MCPA-2-ethylhexyl ester is a systemic, post-emergent herbicide used for the selective control of annual and perennial broad leaved weeds in cereals and other specific crops.
Ethyl acetate, Analytical Standard, ≥99.9% (GC), MilliporeSigma™ Supelco™
Ethyl acetate may be used as an extractant solvent in the analysis of moxalactum in serum samples using high performance liquid chromatography (HPLC).
Bromfenac sodium, Thermo Scientific™
CAS: 91714-93-1 Molecular Formula: C15H11BrNNaO3 Molecular Weight (g/mol): 356.15 MDL Number: MFCD03701673 InChI Key: HZFGMQJYAFHESD-UHFFFAOYSA-M IUPAC Name: sodium 2-[2-amino-3-(4-bromobenzoyl)phenyl]acetate SMILES: [Na+].NC1=C(CC([O-])=O)C=CC=C1C(=O)C1=CC=C(Br)C=C1