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2,4-Dimethoxybenzaldehyde (DMBA) is a reagent used to specifically quantify phlorotannins. This product reacts specifically with 1,3-and 1,3,5-substituted phenols (e.g., phlorotannins) to form a colored product. [1]
2,4-Dimethoxybenzaldehyde, a reagent used to specifically quantify phlorotannins; para-Dimethylaminobenzaldehyde, a reagent used in Ehrlich's reagent and Kovac's reagent; 7,12-Dimethylbenz(a)anthracene, an immunosuppressant and powerful laboratory carcinogen; 1,3-Dimethylbutylamine, a designer stimulant sometimes found in dietary supplements
In enzymology, a lignin peroxidase (EC 1.11.1.14) is an enzyme that catalyzes the chemical reaction. 1,2-bis(3,4-dimethoxyphenyl)propane-1,3-diol + H 2 O 2 3,4-dimethoxybenzaldehyde + 1-(3,4-dimethoxyphenyl)ethane-1,2-diol + H 2 O
βk-2C-B is a designer drug, more specifically it is the beta keto analogue of the controlled substance 2C-B (2,5-dimethoxy-4-bromophenethylamine) which was first synthesized by Alexander Shulgin. It is unknown who first synthesized βk-2C-B, but it first appeared on the market mid-2013 as a recreational drug. [ 1 ]
Dimethoxybenzaldehyde may refer to: 2,4-Dimethoxybenzaldehyde (DMBA) 2,5-Dimethoxybenzaldehyde; Veratraldehyde (3,4-dimethoxybenzaldehyde) This page was last edited ...
2,5-Dimethoxybenzaldehyde is an organic compound and a benzaldehyde derivative. One of its uses is the production of 2,5-dimethoxyphenethylamine, also known as 2C-H . 2C-H is used to produce many other substituted phenethylamines such as 2C-B , 2C-I and 2C-C .
2C-B (4-bromo-2,5-dimethoxyphenethylamine), also known as Nexus, is a synthetic psychedelic drug of the 2C family, mainly used as a recreational drug. [ 2 ] [ 1 ] [ 4 ] It was first synthesized by Alexander Shulgin in 1974 for use in psychotherapy .
2,4-Dihydroxybenzaldehyde or β-resorcylaldehyde is a phenolic aldehyde, a chemical compound with the formula C 7 H 6 O 3. It is an isomer of protocatechuic aldehyde (3,4-dihydroxybenzaldehyde). References