ライフサイエンスコーパス: HCl

1 HCl gave amphimedine in 8 steps from tryptamine with an

2 HCl is oxidized to generate Cl2 and protons in the anode

3 HCl was studied experimentally and with density function

4 in for the outer layer, pH 7, and 0.025MTris-HCl.

5 investigate the detection of Fe(3+) in 0.05M HCl+0.05M KCl solution.

6 ling module after elution with 4 mL of 0.05N HCl.

7 d in MeOH and diluted with either MeOH (0.1% HCl) or buffers to obtain final concentrations between 5

8 n solution containing 200microL of 6molL(-1) HCl.

9 sonication cycle = 74%), using 0.5 mol L(-1) HCl as the extractant, the limits of quantification were

10 upport, 0.5 mol L(-1) NaCl and 4.2 mol L(-1) HCl as the extraction solution, and 1 min stirring time.

11 15min; and elution solvent, 2mL of 1molL(-1)HCl.

12 nly exhibits strong acid resistance (pH = 1, HCl) but also remains intact even when immersed in satur

13 our discovery of the parent compound (+/-)-1.HCl as an anti-microtubule agent.

14 more potent than the parent compound (+/-)-1.HCl.

15 ons were determined to be 60 degrees C, 0.1M HCl in methanol and 3h without added epicatechin.

16 (E124) reaches maximum in acidic medium (1M HCl - pH 1).

17 tion is also maximal in an acidic medium (1M HCl - pH 2).

18 143) is absorbed in the wider area of pH (1M HCl - pH 6).

19 DGE.2 H2O, BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were deter

20 E.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were determined in archived biosolid samples collec

21 A mixture of diluted HNO(3)+HCl+HF, was selected as the best option for the achievem

22 V) from the adsorbent was 17% when using 30% HCl and 85% with 1M NaOH solution.

23 In addition, 30.HCl inhibited cancer cell proliferation regardless of Pg

24 Compound 30.HCl is water-soluble and easily synthesized and serves a

25 The most potent compound 30.HCl was a one to two digit nanomolar inhibitor of most t

26 In vivo efficacy of 30.HCl was demonstrated against a triple negative breast ca

27 rate from minced skins extracted with pH 2.4 HCl containing 23.6KU/g pepsin was the highest (64.19%).

28 ha-form after 3h in 40% NaOH or 1-3 h in 40% HCl solution, and alpha-chitin obtained from NaOH treatm

29 eta(2)-antagonist (betaxolol and ICI-118,551 HCl).

30 % v/v ethanol:water, 85:15% v/v ethanol:1.5N HCl, and ethanol).

31 ollected in a 1-mL fraction of 90% EtOH/0.9N HCl after removal of (68)Ge-breakthrough in a washing st

32 composition of a HfO2/Al2O3 gate stack on a HCl wet-cleaned In0.53Ga0.47As substrate by comparing th

33 Calcium-based scrubbers designed to absorb HCl and SO(2) from flue gases can also remove oxidized m

34 pproximately 500 muL) of an ammonium acetate/HCl (pH 4.5) solution suitable for direct radiolabeling.

35 a volume of 200-400 muL of ammonium acetate/HCl solution (1 M, pH 3.5-4.0) within 10 min.

36 Cl3) catalyst together with a Bronsted acid (HCl) catalyst in aqueous media is investigated.

37 acid hydrolysis using 6 M hydrochloric acid (HCl), followed by amino acids derivatization using N,O-b

38 h then combine to produce hydrochloric acid (HCl).

39 solvents or concentrated hydrochloric acid (HCl).

40 chloride (FeCl3, 1 M) and hydrochloric acid (HCl, 3 M) and continuously drawing the newly released gr

41 In the presence of acid (HCl) or base (NaOH), complex 2 produces TMSCH(2)OH.

42 ) extract was examined in the strong acidic (HCl+H2SO4) solution.

43 uminum from primary sludge by acidification (HCl or H2SO4), followed by separation using centrifugati

44 mplest CI, CH2 OO, with two inorganic acids, HCl and HNO3 , both of which are present in polluted urb

45 ine atoms with butenes, that the Cl addition-HCl elimination pathway occurs from an abstraction-like

46 Poly (9-(2-diallylaminoethyl)adenine HCl-co-sulfur dioxide) (Poly A) deposited on silica nano

47 onalized with the polycation poly(allylamine HCl) in a manner that depends on the NOM-to-DNP concentr

48 Two catalysts, an amine HCl salt and a bisthiourea, work in concert to enable th

49 he emphasis in previous studies, ClNO(2) and HCl are dominant primary chlorine atom sources for the L

50 The combined use of trifluoroacetic acid and HCl during the synthesis results in a highly crystalline

51 the presence of carbonyl groups, CF3COOH and HCl for basic sites of different strength, and O3 and NO

52 moderate temperatures by combining CrCl3 and HCl.

53 d DNA (dsDNA) with acetone, ethanol, H2S and HCl.

54 g(HSO4)2 salt solutions as well as H2SO4 and HCl acid solutions are investigated by means of vibratio

55 eridine-N-oxyl) in combination with HNO3 and HCl (10 mol % each).

56 and in the literature dilute acids, HNO3 and HCl, showed the highest extracted iAs wheras dilute NaOH

57 Microwave power, methanol and HCl concentration significantly (p<0.05) affect extracti

58 es, cyclization, halogen atom migration, and HCl (HBr) elimination.

59 ses only a common base and an acid, NaOH and HCl to initiate and stop the polymerization reaction, re

60 d that the minor constituents (SO2, NOx, and HCl) significantly modify the percentages of Hg(2+) in t

61 se a MtBE-H2O (1:1) system with 10mM TEA and HCl was applied leading to a phenolic fraction, free of

62 olysis requires the action of both water and HCl.

63 ve solid, prepared by treatment of anhydrous HCl with [Et3 SiHSiEt3 ][CHB11 F11 ].

64 lateral turns after injection of apomorphine HCl (p<0.05).

65 s by extraction into toluene from an aqueous HCl solution; unlike current processes, reverse phase tr

66 een carried out in universal buffer, aqueous HCl, and artificial seawater media.

67 ed readily in the presence of dilute aqueous HCl to give the final quinoline products.

68 ocarbamates with Tin(II) chloride in aqueous HCl.

69 study for adduct hydrolysis in 0.1 M aqueous HCl determined that (Fur)dG was the most acid-sensitive

70 Etching of the MOF with 1 M aqueous HCl followed by 5% H2O2 yielded a titania replica that r

71 nobenzidine and catalytic amounts of aqueous HCl.

72 ) which is about 50-55 % of state-of-the-art HCl electrolysis processes.

73 The optimum conditions were determined as HCl concentration between 0.41 and 0.44mol/L, methanol v

74 of Et4N[H3(BAr(F)3)2], strong acids such as HCl induce H2 release to give the chloride Et4N[(CO)(CNB

75 ropyl paraben (PrP), BADGE.2H(2)O, and BADGE.HCl.H(2)O were the predominant compounds found in dust s

76 oducts (BADGE.H(2)O, BADGE.2H(2)O, and BADGE.HCl.H(2)O).

77 r derivatives (BADGE.2 H2O, BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.

78 BADGE.H2O, BADGE.HCl.H2O, BADGE.2 HCl, BADGE.HCl, BFDGE.2 H2O, and BFDGE.2 HCl) were determined in ar

79 products, in addition to propenes, are base.HCl and olefin-bound, cyclometalated dimers [RuCl(kappa(

80 s (prednisolone acetate [generic], betaxolol HCl [Betoptic; Alcon Laboratories Inc., Fort Worth, TX],

81 d and selective Markovnikov addition of both HCl and HBr across several alkene classes under mild rea

82 The DPI-BP/HCl adduct possesses a more planar configuration than DP

83 ) into the solution to dissociate the DPI-BP/HCl adduct.

84 group of DPI-BP to convert it into a DPI-BP/HCl adduct.

85 cted with either the analgesic buprenorphine-HCl or saline every 12 hrs; injections were started one

86 ther cognitive-behavioral therapy, bupropion HCl, or pill placebo.

87 y HPLC-DAD) and proanthocyanidins (n-butanol/HCl assay), reducing capacity (ferric ion reducing antio

88 cyanidins by depolymerisation with n-butanol/HCl, flavonols by HPLC-DAD, reducing capacity by ferric

89 m Ajka, Hungary is neutralized to < pH 10 by HCl, gypsum, or seawater addition.

90 troscopic (UV-visible) investigations and by HCl-augmented computational modeling.

91 H is redox-dependent and can be estimated by HCl leachable sediment Fe(III)/Fe ratio with typical Fe

92 ed into 3 groups in which ALI was induced by HCl inhalation: pigs studied in the supine position with

93 onate and sodium glutarate salts resulted by HCl evaporation from dehydrating particles.

94 found to be affected in aqueous solutions by HCl, NaCl, KCl, and CaCl2 and in acetonitrile by CF3COOH

95 ethyl-3-(3-dimethylaminopropyl) carbodiimide HCl (EDC) has recently been investigated for its effecti

96 repare 9, it was found that adding catalytic HCl and LiCl enabled higher yields.

97 Nevertheless, LinA and LinB catalyzing HCl elimination and hydrolytic dehalogenations, respecti

98 Internal stress in bent CFZ-HCl led to photoelastic effects on the azimuthal orienta

99 ocrystals-the hydrochloride salt of CFZ (CFZ-HCl)-has a corrugated packing along the (001) face and w

100 hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation.

101 , at the 2sigma level, in hydrogen chloride (HCl), the main stratospheric chlorine reservoir, startin

102 as well as the bioactive compound Cinacalcet HCl.

103 using data from the Evaluation of Cinacalcet HCl Therapy to Lower Cardiovascular Events trial, a plac

104 pproach failed when the leaving group was Cl/HCl or Br/HBr, both for anionic and neutral nucleophiles

105 s are activated with SOCl(2) or concentrated HCl and then treated with trimethylaluminum, affording t

106 antly up to 20-fold compared to conventional HCl mediated extraction, depending on the mushroom speci

107 yzed cleavage of the resulting cyclopropane (HCl), further improvements in a unique intramolecular cy

108 e was optimized by a 3(2) factorial design (%HCl in methanol, temperature, and time) and response sur

109 alization of soil samples with HF and dilute HCl and recovery of the SOM fraction solubilized in the

110 ion in vivo or by treatment with cold dilute HCl or with excess borate in vitro) enhanced the GIPCs'

111 nt has been developed that allows for dilute HCl (0.05N) to efficiently elute metal-impurity-free (68

112 pensive and nontoxic reagents (NaCl, diluted HCl, water).

113 Metformin (MF) (1,1-dimethylbiguanide HCl) is one of the most commonly used oral antihyperglyc

114 )-2-(2-quinolin-2-yl-vinyl)-benzene-1,4-diol HCl) hereafter designated Q8.

115 iminates the need to buy new Cl2 and dispose HCl waste.

116 ent with either gaseous water or gaseous dry HCl.

117 ciently promoted by catalytic amounts of dry HCl.

118 plex and the beneficial effect of added Et3N.HCl on yield and enantioselectivity is elucidated: chlor

119 extracts containing it, diluted with ethanol-HCl to assess total flavonoids and anthocyanins in the s

120 HCl (100:1, v/v) (W2), ethanol (E3), ethanol:HCl (100:1, v/v) (E4), dichloromethane (D5) and hexane (

121 of cation-exchange chromatography using EtOH/HCl medium has been developed.

122 s of protonation and activation energies for HCl addition across the multiple bonds have been calcula

123 ichloroethene (DCE), due to competition from HCl formation.

124 OH)2 addition which limited pH declines from HCl, volatile fatty acids (VFAs), and inorganic carbon (

125 x that provides a route to H2 evolution from HCl.

126 losing the photocycle for H2 generation from HCl.

127 Onsite Cl2 regeneration from HCl is highly desirable as it eliminates the need to buy

128 Gaseous HCl as a by-product is often produced from chlorination

129 A gaseous HCl electrolysis with Fe(3+) /Fe(2+) redox-mediated cath

130 ic chlorine in the presence of H2 to gaseous HCl, was coupled to a dual-detection system, combining a

131 as well as being a source of halogen gases (HCl, ClNO2, etc.).

132 Ps were also more cytotoxic than gemcitabine HCl in the deoxycytidine kinase deficient (CCRF-CEM/dCK(

133 Similar to gemcitabine HCl, GemC18-NPs induced apoptosis through caspase activa

134 kdown of Atg9a or treatment with gemcitabine HCl resulted in enhanced stimulator of IFN genes-mediate

135 The reaction utilizes in situ generated HCl as the source of both the Cl(-) and H(+) and is cata

136 m the slides by treatment with 0.1 M glycine.HCl buffer, pH 2.6, for 30 min and regenerated by shakin

137 olished by the denaturants triton X-100, Gua-HCl, Gua-thiocyanate, SDS and urea in a dose-dependent m

138 of the alpha2 adrenergic agonist, guanfacine HCl, on responses to stress and drug cue in a group of c

139 inst chemical denaturants urea and guanidine HCl.

140 ich were measured independently by guanidine HCl-induced unfolding titrations using purified proteins

141 as only slightly more resistant to guanidine-HCl induced denaturation compared to unbound protein.

142 H2O, CO2, SO2, O2, H2, H2S, HCl, chlorinated hydrocarbons, NO, and other trace gases

143 ion bias due to formation of byproducts HCN, HCl, and H2S.

144 r is produced by placing the carbides in HF, HCl or NaCl solutions and applying anodic potentials.

145 , for other variables, such as solvent (HNO3:HCl), final concentration (1.7molL(-1)) and time (26min)

146 the species present in the crystal, 5Me-HQE.HCl, was lost HCl upon sublimation but did not tautomeri

147 transfer between O2 and liquid hydrocarbons, HCl dissociation in salty water, and super-Maxwellian he

148 ater than that of gemcitabine hydrochloride (HCl).

149 ) by addition of 2.0 mL of 10% hydroxylamine HCl, the system was applied to the total iron.

150 e structure sensitive reaction to illustrate HCl surface structure effects.

151 t on polyaniline film using Fe(2+)/Fe(3+) in HCl as the redox system shows five distinct linear segme

152 hese challenges and characterize actinium in HCl solutions using X-ray absorption spectroscopy and mo

153 of Au obtained by anodic stripping of Au in HCl solution was used to evaluate the average diameter o

154 tammetry of AuNPs after their dissolution in HCl.

155 y comparisons between Ac(III) and Am(III) in HCl solutions indicate Ac(III) coordinates more inner-sp

156 It can be strongly suppressed in HCl medium by partial hydrolysis of THB with optimal con

157 BAB), and sodium tetrahydridoborate (THB) in HCl and HClO4 media, in the presence or absence of L-cys

158 The parent reagent and its HCl salt present stability and detonation risks, but the

159 5mL of 1mol/L HCl was used as eluent.

160 1 mL of 1 mol/L HCl and 5% thiourea was used as eluent.

161 A lidocaine HCl (Xylocaine) injection on the midline at the rostroca

162 For the latter, common reagents like HCl, Na2CO3, glycine buffer, or SDS are employed.

163 resent in the crystal, 5Me-HQE.HCl, was lost HCl upon sublimation but did not tautomerize.

164 6-dicarboxylic acid hydrochloride (LY3020371.HCl, 19f), a potent, selective, and maximally efficaciou

165 ency using a standard acid wash with a 1.0 M HCl solution followed by neutralization with a 0.1 M NaO

166 H (pH: 13.4) was added to 3.7 muL of 0.058 M HCl (pH: 1.24).

167 Im chi((2)) spectra of 1.1 M H2SO4 and 1.1 M HCl acid solutions indicate that HSO4(-) ions have a sim

168 .0 x 10(-3) to 2.6 x 10(-5) M, in both 0.1 M HCl and 0.1 M HNO(3).

169 e sensor is regenerable by treating with 1 M HCl and can be used for multiple analysis with little re

170 procedures for polonium samples (0.1 to 1 M HCl).

171 optimized (0.05 mg of Cu(2+) in 10 mL of 1 M HCl); these compare advantageously with conventional pre

172 h 1.1 M H2SO4 being more enhanced than 1.1 M HCl.

173 y inert in very harsh conditions such as 2 M HCl, with no dissociation being observed for at least 5

174 A loss of ca. 50% of 0.5 M HCl-extractable Fe(II) [5-10 mmol Fe(II) L(-1)] and dete

175 -3-yl]-3-(1-methyl-1H-indo l-3-yl)maleimide, HCl, bisindolylmaleimide X, HCl), GRK2 [C-terminal GRK2

176 To do this, we administered MDMA-HCl (100 mg p.o.) and, separately, placebo (ascorbic aci

177 rst, structural models of erythro-mefloquine HCl compatible with NMR-derived (3)J(HH) scalar coupling

178 tant antimalaria drug rac-erythro-mefloquine HCl has been on the market as Lariam for decades, the ab

179 ignment of 11R,12S to (-)-erythro-mefloquine HCl is correct.

180 as depolymerized, using 0.1 or 1M methanolic HCl, with (+)-catechin, (-)-epicatechin, or (-)-epigallo

181 Minocycline HCl 1 mg microspheres were applied on biofilms on days 2

182 er dimer and trimer, HCl clusters, and mixed HCl-water clusters are the major topics, but related wor

183 nd the foam was dissolved in 300 muL of 1 mM HCl.

184 cumene; donor, 1 muL of basic drugs in 10 mM HCl; and extraction potential, 250 V), experimentally de

185 The formyl-H KIEs are (D)k = 0.80 in 200 mM HCl, (D)k = 0.77 in 50 mM HCl, (D)k = 0.75 in pure water

186 lvent (D2O) KIEs are (D2O)k = 0.20 in 200 mM HCl, (D2O)k = 0.81 in 50 mM HCl, and (D2O)k = 4.2 in pur

187 mu-EME conditions (acceptor, 1 muL of 25 mM HCl; FLM, 1 muL of 4-nitrocumene; donor, 1 muL of basic

188 k = 0.80 in 200 mM HCl, (D)k = 0.77 in 50 mM HCl, (D)k = 0.75 in pure water, (D)k = 0.88 in 50 mM NaO

189 = 0.20 in 200 mM HCl, (D2O)k = 0.81 in 50 mM HCl, and (D2O)k = 4.2 in pure water.

190 ater, and the (63)Zn was eluted using 0.05 N HCl in 90% acetone.

191 Increases in 0.5 N HCl-extractable Fe(II) were observed in incubated sedime

192 rous, and stable in boiling water, acid (9 N HCl), and base (3 N NaOH).

193 rkable stability in boiling water, acid (9 N HCl), and base [TpBD (MC) in 3 N NaOH and TpPa-2 (MC) in

194 d by immersing carbon electrodes in NR-NaNO2-HCl solution.

195 ild heating react via elimination of neutral HCl.

196 have similar concentrations of SO2, NO, NO2, HCl, and H2O, the proportion of Hg(0)/Hg(2+) is similar

197 Even in the absence of HCl, hydrolysis of Cr(III) decreases the solution pH, an

198 surements to be derived from the activity of HCl reported by the sensor system over the range of ocea

199 1 transformation involves formal addition of HCl across the Mo horizontal lineN imido bond through in

200 The oxidative addition of HCl to 2 selectively yields the cis-hydride-alkylidyne c

201 Stoichiometric addition of HCl to the Co(I)-(N2) cleanly affords the Co(III) hydrid

202 otoredox catalyst system for the addition of HCl, HF and also phosphoric and sulfonic acids to alkene

203 R(regrowth)) simply by varying the amount of HCl added to the reaction solution.

204 When the amount of HCl was between these two extremes, we obtained Pd octah

205 In contrast, with a small amount of HCl, all of the newly formed Pd(2+) ions could be quickl

206 With a large amount of HCl, etching dominated the process (R(etching) >> R(regr

207 ent to continuously release small amounts of HCl by thermolytic elimination.

208 mium metal to form H(2) and minor amounts of HCl.

209 ontrol is determined by the concentration of HCl in the water phase of the microemulsion.

210 The optimal concentration of HCl was 2 mol L(-1); the optimal concentration of NaBH4

211 ediment containing a higher concentration of HCl-extractable Fe(II).

212 With high concentrations of HCl (e.g., 1.2-1.5 M), all aggregates break up and the k

213 Additionally, using high concentrations of HCl further reduces the production of the less volatile

214 med not only that very low concentrations of HCl generated from the solvent were responsible for the

215 stric conditions with high concentrations of HCl.

216 Subsequent base-induced beta-elimination of HCl proceeds selectively to give nitrobenzylic alpha-flu

217 2) g(-1), respectively, only when 2 equiv of HCl (0.22 M) was used.

218 The generation of HCl at room temperature from a mixture of sodium chlorid

219 oved from the polymeric matrix using 5 mL of HCl (2 mol.L(-1)) as the eluting solvent.

220 neamino)-benzonitrile (1) in the presence of HCl to produce 2-chloro-3-phenyl-4(3H)-quinazoliniminium

221 ed with a dipyrrylmethane in the presence of HCl, followed by oxidation with ferric chloride, to give

222 were analyzed in solution in the presence of HCl.

223 Release of HCl from this salt can be manifested in chlorination and

224 (rac-BINAP) was detected from the release of HCl in the dehydrogenation and subsequent reaction with

225 -dibromophenol as a stoichiometric source of HCl to facilitate catalyst turnover.

226 work represents the first successful use of HCl, the simplest strong Bronsted acid, as an efficient

227 Simple adjustment of the amounts of NH(2)OH.HCl introduced enables this particle shape evolution.

228 ported by systematic investigations based on HCl titration and dynamic light scattering measurements.

229 )) with 100% efficiency with the use of only HCl and NaBH4 as the reagents.

230 results reported here show that the optimal HCl percentage in the water phase is about 25% to obtain

231 n or concentration of the parent compound or HCl salt and will facilitate the use of hydrogen sulfate

232 urn to the outward-facing state in a KCl- or HCl-bound form.

233 rivatives were obtained by saponification or HCl acidolysis of o-boronato-phosphonium amino esters, r

234 arison with the CH method, the pepsin-HCl (P-HCl) method is simpler, avoiding solvent evaporation, di

235 s of PAni doped with hydrochloric acid (PAni-HCl) in an effort to circumvent issues associated with c

236 In summary, sputtered PAni-HCl films exhibit quantifiable, reversible behavior upon

237 racts were digested with a mixture of pepsin-HCl for 2 h, followed by a 2 h incubation with pancreati

238 In comparison with the CH method, the pepsin-HCl (P-HCl) method is simpler, avoiding solvent evaporat

239 e within the NU-1000 pores via a vapor-phase HCl treatment, a silica layer is created on the inner wa

240 ng opening of trans-2-phenylcyclopropylamine.HCl occurs at the distal (C2-C3) bond.

241 Photodriven HCl splitting to produce solar fuels is an important goa

242 Propranolol HCl, as well as very small sugar particles from the pell

243 starter cores were layered with propranolol HCl and subsequently coated with Kollicoat SR, plasticiz

244 x10(-4)molkg(-1) thiamine HCl and pyridoxine HCl solutions.

245 35)molkg(-1) thiamine HCl(aq) and pyridoxine HCl(aq) solutions over temperature range (288.15-318.15)

246 r received HCl inhalation or did not receive HCl inhalation.

247 ual to 35 cm of H2O and that either received HCl inhalation or did not receive HCl inhalation.

248 pport, concentration of extraction solution (HCl and NaCl), and stirring time, were investigated by t

249 ling that the compounds function as 'strict' HCl cotransporters.

250 (The HCl-exchanged QBs are insufficiently stable for elementa

251 e, 15.6-21.3 per thousand, was found for the HCl-extractable inorganic delta(18)O(p), with the except

252 The important autocatalytic effect of the HCl reaction product was confirmed by spectroscopic (UV-

253 The applicability of the HCl/HFIP method is illustrated by the synthesis of a sul

254 carried out in 1.0x10(-4)molkg(-1) thiamine HCl and pyridoxine HCl solutions.

255 0.05, 0.15, 0.25 and 0.35)molkg(-1) thiamine HCl(aq) and pyridoxine HCl(aq) solutions over temperatur

256 ow how the exposure of plant-based fibers to HCl vapor results in rapid degradation with simultaneous

257 arger relative conversion of source gases to HCl.

258 tected monosaccharides that are subjected to HCl/HFIP treatment.

259 cohols, which are normally unreactive toward HCl catalysis.

260 VP of the water dimer and trimer, HCl clusters, and mixed HCl-water clusters are the major

261 imum response within 2s at pH 8.5 (0.1M Tris-HCl) and 35 degrees C, when operated at 20 mV s(-1).

262 as achieved with crude extract at pH 7, Tris-HCl binding buffer at pH 7 and the use of 300 mM imidazo

263 Phosphate and Tris-HCl buffers decrease the signal intensity measured in Fe

264 ion Tg in a freeze-concentrated buffer (Tris-HCl).

265 ons of ionic strength (163 mM) in 50 mM Tris-HCl (pH 7.4) at 37 degrees C.

266 ssium glutamate and 8 mM MgCl2 or 10 mM Tris-HCl and 200 mM KCl, with or without 0.5% Tween added to

267 ed directly from a 150 mM KCl and 25 mM Tris-HCl buffer at pH 7 that is widely used in protein chemis

268 ysis buffer with high concentrations of Tris-HCl and sodium dodecyl sulfate as well as exposure to hi

269 On the other hand, the use of Tris-HCl as binding buffer gave higher purification performan

270 ction buffers (phosphate buffer saline, Tris-HCl and NaCl) on the extraction efficiency of total prot

271 s higher using 0.5M NaCl as compared to Tris-HCl and phosphate buffer saline.

272 An extraction procedure using Tris-HCl buffer solution was employed in order to extract wat

273 -46.5%) bound to the column eluted with Tris-HCl buffer, pH 7.5 with a yield up to 76.6%.

274 ) and Cetylpyridinium chloride (CPC) in Tris/HCl buffer, pH 8.5.

275 h and 121 degrees C/30 min, at pH 1-7 using HCl, formic or citric acid as acidulants.

276 to compare the effects of pH adjusted using HCl vs CO2.

277 ) and acid-soluble ash (ASA) fractions using HCl.

278 ve assisted extraction was carried out using HCl 1molL(-1) in order to maintain the integrity of the

279 rbal powder, 0.1% m/v citric acid and 2% v/v HCl was injected into the VG-ICP-MS system for the deter

280 s of these bio-residues in water (W1), water:HCl (100:1, v/v) (W2), ethanol (E3), ethanol:HCl (100:1,

281 res based on subtle pKa differences, whereas HCl addition leads to a rapid formation of mixed compone

282 c(V)O2}(+) core into {(99)Tc(V)OCl}(2+) with HCl as the H(+) and Cl(-) source.

283 (P)N(H))] is generated by reaction of 3 with HCl or by direct photolysis of 2 in chlorobenzene.

284 Si:L (L: = C{N(2,6-(i)Pr2C6H3)CH}2) (8) with HCl.NC5H5 results in carbene-stabilized Si2Cl2 (2) and s

285 ives by deoxygenation and aromatization with HCl/EtOH.

286 how fluorescence quenching upon binding with HCl likely due to the smaller pi-conjugation structure,

287 c acid for total As and Sb, and boiling with HCl for total Se.

288 nocatalyst that operates in combination with HCl.

289 Cu and CA could be recovered completely with HCl.

290 htforward removal of the sulfinyl group with HCl yields the highly enantiomerically enriched amine hy

291 d Sb(III) ions were removed by leaching with HCl (50%v/v) and the polymer was characterised by FT-IR

292 fast; at 295 K, the reactions of CH2 OO with HCl and HNO3 have rate constants of 4.6x10(-11) cm(3) s(

293 Particle surfaces reacted with HCl accumulated less water than acid-free surfaces due t

294 )O was found during the reaction of THB with HCl, H2SO4, and HClO4, while HG from CH3COOH or TRIS buf

295 BP and is expected to bind the same way with HCl.

296 by the simple reaction of metallic zinc with HCl in water for H2 and DCl in deuterated water for D2.

297 thite nanoparticles reacted with and without HCl and NaCl were resolved using vibrational spectroscop

298 utants (HAPs), including SO(2)/SO(3), NO(x), HCl, particulate matter, mercury, and other trace elemen

299 -3-yl)maleimide, HCl, bisindolylmaleimide X, HCl), GRK2 [C-terminal GRK2 peptide overexpression and s

300 rder were randomized to placebo or yohimbine HCl (10.8 mg) 1 hour before each of four exposure sessio