-
8223431000Analysis Note Assay (GC, area%): ≥ 99.0 % (a/a) Melting range (lower value): ≥ 77 °C Melting range (upper value): ≤ 80 °C Identity (IR): passes test
-
39246-50MGFind more information here: Neonicotinoids see also 46451 Application Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
-
27221-1LAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having pungent odor.
-
27225-1L-RAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having pungent odor.
-
27225-2.5L-RAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having pungent odor.
-
27225-200L-RAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having pungent odor.
-
27225-500ML-RAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having pungent odor.
-
33209-1LAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having a pungent odor.
-
33209-2.5LAcetic acid is an organic carboxylic acid. It is a hygroscopic liquid having a pungent odor.
-
338826-100MLApplication Acetic acid can be used as a catalyst: For the solvent-free one-pot condensation of indoles with aryl or heteroaryl aldehydes to synthesize di(indolyl)methanes. In the Pictet-Spengler reaction of substituted tryptamines with cyclic
-
338826-25MLApplication Acetic acid can be used as a catalyst: For the solvent-free one-pot condensation of indoles with aryl or heteroaryl aldehydes to synthesize di(indolyl)methanes. In the Pictet-Spengler reaction of substituted tryptamines with cyclic
-
338826-4X100MLApplication Acetic acid can be used as a catalyst: For the solvent-free one-pot condensation of indoles with aryl or heteroaryl aldehydes to synthesize di(indolyl)methanes. In the Pictet-Spengler reaction of substituted tryptamines with cyclic