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B-Base

Experiments were carried out on samples, made of austenitic steel with thickness from 10 to 50 mm using equipment, described above. The samples were a) multipass austenitic weld and b) base metal. [Pg.731]

Figure 2 a) multipass austenitic weld and b) base metal. [Pg.732]

A simple decision-making problem is I measure variable x of a population A and the same variable xof a population B. I get (slightly) different results. Is there areal difference between populations A and B based on the difference in measurements, or am I only seeing different parts of the distributions of identical populations ... [Pg.14]

The reaction takes place extremely rapidly and if D2O is present in excess all the alcohol is con verted to ROD This hydrogen-deuterium exchange can be catalyzed by either acids or bases If D30 is the catalyst in acid solution and DO the catalyst in base wnte reasonable reaction mech anisms for the conversion of ROH to ROD under conditions of (a) acid catalysis and (b) base catalysis... [Pg.186]

Eig. 1. Schematics of (a) acid-cataly2ed and (b) base-cataly2ed siHca gels showing the differences in microstmcture and surface functional groups. [Pg.1]

The free base of compound (17) is Rhodamine B base [509-34-2] (Solvent Red 49 Cl 45170 1). The phosphotungstomolybdic acid salt of (17) is Pigment Violet 1 [1326-03-0] Cl45170 2). Pigment Red 173 [12227-77-9] Cl45170 3) is the corresponding aluminum salt. [Pg.400]

Treatment of halomycin B (55) using nitrous acid yields rifamycin S (24) and the pyrroHdine (57) as shown in Figure 6. The halomycin B stmcture was confirmed by heating rifamycin O (23) and (57) in tetrahydrofiiran to yield halomycin B (20) which can also be converted to rifamycin S by electrochemical oxidation (213). Upon treatment with nitrous acid, halomycin A (54) yields rifamycin S along with the pyrroHdine (58). The stmcture for halomycin C (56) was deterrnined to be 20-hydroxy halomycin B based on mass spectral data (212). [Pg.500]

MAO is known to occur in at least two forms, MAO A and MAO B, based on substrate selectivity, inhibition by various dmgs, and cloning experiments. Clorgyline [17780-72-2] is a specific inhibitor of MAO A, which displays a substrate specificity for NE and serotonin. Deprenyl [2323-36-6] is a selective inhibitor of MAO B, and displays a substrate preference for P-phenylethylamine and benzyl amine. Dopamine and tyramine are substrates for both enzymes. [Pg.358]

The predominance of a-substituted products in the reaction of 2,4,6-tribromopyridine in phenol solution may result from competitive attack by free phenol in preference to attack by the phenoxide ion reagent involving structures 18 (B = base) or 19. A wealth of chemistry awaits elucidation by physical-organic studies. [Pg.312]

B = base pressure drop for control valve t dth valve in wde-open position, psi. (see list above). [Pg.94]

NOTE Calculations are based on formulas in Appsndix A, API RP7C Table b based on API RP7C. Tables 2.1 and 2.2. [Pg.740]

Hydrophobicity plots of AQPs indicated that these proteins consist of six transmembrane a-helices (Hl-H6 in Fig. la) connected by five connecting loops (A-E), and flanked by cytosolic N- and C-termini. The second half of the molecule is an evolutionary duplicate and inverse orientation of the first half of the molecule. Loops B and E of the channel bend into the membrane with an a-helical conformation (HB, HE in Fig. lb) and meet and each other at their so-called Asn-Pro-Ala (NPA) boxes. These NPA motifs are the hallmark of AQPs and form the actual selective pore of the channel, as at this location, the diameter is of that of a water molecule (3 A Fig. la and b). Based on the narrowing of the channel from both membrane sides to this small... [Pg.214]

Decide which member of each of the following pairs is the stronger acid or base in water (a) acid HF or HIO, (b) base NOz or CN. ... [Pg.530]

Using Table 5.6 (see p. 156), propose a sequence for glu-fibrinopeptide B based on the product-ion MS-MS spectrum shown in Figure 4.20. [Pg.178]

Route (b), based on an aliphatic Friedel-Crafts reaction, gives a good yield of (31) which is duly acylated with ketene dimer. [Pg.400]


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See also in sourсe #XX -- [ Pg.33 , Pg.34 , Pg.35 , Pg.36 , Pg.37 , Pg.38 , Pg.39 ]




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