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Triethylamine is prepared by the alkylation of ammonia with ethanol: [10]. NH 3 + 3 C 2 H 5 OH → N(C 2 H 5) 3 + 3 H 2 O. The pK a of protonated triethylamine is 10.75, [4] and it can be used to prepare buffer solutions at that pH.
C 6 H 7 NO 3 S: metanilic acid: 121-47-1 C 6 H 7 N 3 O: isoniazid: 54-85-3 C 6 H 7 N 3 O: nicotinic acid hydrazide: 553-53-7 C 6 H 7 P: phenylphosphine: 638-21-1 C 6 H 7 Si: phenyl silyl radical: 72975-30-5 C 6 H 8: cyclopropylidene cyclopropane: 27567-82-4 C 6 H 8: ethynylcyclobutane: 50786-62-4 C 6 H 8 AsNO 3: arsanilic acid: 98-50-0 C 6 H 8 ...
Methyl anisate is the methyl ester of p-anisic acid.It is found in star anise.. It is an organic compound commonly used within the food industry. It is also commonly employed as a fragrance for certain perfumes.
Screenshot of the CAS Common Chemistry database with information about caffeine ().. A CAS Registry Number [1] (also referred to as CAS RN [2] or informally CAS Number) is a unique identification number, assigned by the Chemical Abstracts Service (CAS) in the US to every chemical substance described in the open scientific literature, in order to index the substance in the CAS Registry.
CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA) 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0 C 20 H 25 N 30: Lysergic acid diethylamide (LSD) 50–37–3 C 123 H 193 N 35 O 37: Common serum albumin (macromolecule) 9048–49–1 Ca(AlH 4) 2: calcium ...
Benzethonium chloride exhibits a broad spectrum of microbiocidal activity against bacteria, fungi, mold, and viruses. Independent testing shows that benzethonium chloride is highly effective against such pathogens as methicillin-resistant Staphylococcus aureus, Salmonella, Escherichia coli, Clostridioides difficile, hepatitis B virus, hepatitis C virus, herpes simplex virus (HSV), human ...
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The crystal structure called Form I is a disappearing polymorph that cannot be produced by researches anymore while Form II and III still exist. [6] The reason for this is that Form I is converted to another polymorph upon contact with a seed crystal and most places are contaminated with tiny amounts of Form II or III that are enough to prevent any viable amounts of Form I to be produced.