Search results
Results from the WOW.Com Content Network
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.
Chemical formula Synonyms 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
Chemical Abstracts Service Building B in August 2009. Columbus, Ohio. STN (Scientific & Technical Information Network) International is operated jointly [4] by CAS and FIZ Karlsruhe, and is intended primarily for information professionals, using a command language interface.
Dimethyl sulfoxide can often be used in place of HMPA as a cosolvent. Both are strong hydrogen bond acceptors, and their oxygen atoms bind metal cations.Other alternatives to HMPA include the N,N′-tetraalkylureas DMPU (dimethylpropyleneurea) [10] [11] or DMI (1,3-dimethyl-2-imidazolidinone). [12]
Additionally, EDC can also be used to activate phosphate groups in order to form phosphomonoesters and phosphodiesters. Common uses for this carbodiimide include peptide synthesis, protein crosslinking to nucleic acids, but also in the preparation of immunoconjugates.
N,N′-Dicyclohexylcarbodiimide (DCC or DCCD) [1] is an organic compound with the chemical formula (C 6 H 11 N) 2 C. It is a waxy white solid with a sweet odor. Its primary use is to couple amino acids during artificial peptide synthesis.
This page was last edited on 23 October 2024, at 02:12 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Tetramethylethylenediamine (TMEDA or TEMED) is a chemical compound with the formula (CH 3) 2 NCH 2 CH 2 N(CH 3) 2.This species is derived from ethylenediamine by replacement of the four amine hydrogens with four methyl groups.