Category: 2525-05-5

The author of 《Transition potentials of some triphenylmethane dyes redox indicators》 were Belcher, R.; Brazier, J. N.; Stephen, W. I.. And the article was published in Talanta in 1965. Synthetic Route of C10H14O2 The author mentioned the following in the article:

The transition ranges of 3 triphenylmethane dye redox indicators have been redetermined The figures found in 1F H2SO4 are appreciably higher than earlier values; the new figures are more in accord with the behavior of these indicators when compared with 2,2′-dipyridyl and substituted ferroins. At high acidities the indicators function in the dichromate-Fe(II) system. In a HClO4 medium the figures are significantly higher and fall into a range which accounts for the fact that all 3 dyes function as indicators with hexaperchloratocerate(IV) titrant. The potentials of ferroin and is derivatives are apparently unaffected by change of medium. The experimental process involved the reaction of 4-Butylbenzene-1,2-diol(cas: 2525-05-5Synthetic Route of C10H14O2)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Synthetic Route of C10H14O2

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《The colorimetric determination of molybdenum with polyhydric phenols》 was published in Talanta in 1962. These research results belong to Buchwald, H.; Richardson, E.. Computed Properties of C10H14O2 The article mentions the following:

Polyhydric phenols containing 2 ortho OH groups, such as catechol, 4-methylcatechol, 3,4-dihydroxybenzaldehyde, 3,4-dihydroxybenzoic acid, Tiron, gallic acid (I), pyrogallol, 2,3,4-trihydroxybenzoic acid, 3-methyl-6-sec-propyleatechol, 4-butylcatechol, 2,3,-dihydroxynaphthalene, and Na 2,3-dihydroxynaphthalene-6-sulfonate (II), can be used for the colorimetric determination of Mo. Beer’s law applies in the presence of a large excess of reagent:phenol (≳25:1). Dissolve the sample by fusion, mineral acid, or alkali. If Mo is reduced, oxidize it to Mo(VI) with HNO3, remove interfering ions (by ion exchange, changing the pH, etc.), adjust the soln, to contain 5-100 γ Mo/ml., adjust the pH to 5.2, dilute to 25 ml., measure the absorbance at 420 mμ, and compare with a calibration curve. Higher concns, can be determined with less accuracy at 500-600 mμ. The practical sensitivity for Mo is about 0.1 γ/ml. at 400 mμ. 15 references. The experimental part of the paper was very detailed, including the reaction process of 4-Butylbenzene-1,2-diol(cas: 2525-05-5Computed Properties of C10H14O2)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Computed Properties of C10H14O2

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Alcohol – Wikipedia,
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Safety of 4-Butylbenzene-1,2-diolOn November 8, 2016 ,《Sulfo-and carboxybetaine-containing polyampholytes based on poly(2-vinyl pyridine)s: Synthesis and solution behavior》 appeared in Polymer. The author of the article were Billing, Mark; Elter, Johanna K.; Schacher, Felix H.. The article conveys some information:

We present the synthesis and characterization of zwitterionic homopolymers and copolymers based on poly(2-vinyl pyridine) (P2VP). Different molar masses as well as copolymer compositions of poly(styrene-co-2-vinyl pyridine) (P(2VP-co-S)) were synthesized using RAFT (reversible addition fragmentation chain transfer) polymerization, followed by quaternization of the nitrogen atom by either 1,3-propanesultone (P2VPS, P(2VPS-co-S)) or ethyl-2-bromoacetate, followed by ester hydrolysis (P2VPC, P(2VPC-co-S)). The resulting materials were characterized using SEC, 1H and 13C NMR spectroscopy, elemental anal., and zeta potential measurements. Degrees of functionalization ranging from 33 to 76% could be determined and both P2VPC and P2VPS exhibited good solubility over the entire pH-range. Upon incorporation of increasing amounts of styrene, aqueous solubility decreased and also UCST behavior could be observed in case of P(2VP56,S-co-S44). In the experiment, the researchers used many compounds, for example, 4-Butylbenzene-1,2-diol(cas: 2525-05-5Safety of 4-Butylbenzene-1,2-diol)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.Safety of 4-Butylbenzene-1,2-diol Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

《Inhibition and enhancement of luminol-KIO4-H2O2 chemiluminescence by organic compounds》 was written by Xu, Hong. Electric Literature of C10H14O2 And the article was included in Faguang Xuebao on August 31 ,2006. The article conveys some information:

The inhibition and enhancement of liquid phase CL by organic compounds are of considerable interests in anal. chem. because they can be used for the sensitive detection of numerous compounds The mechanism of inhibition and enhancement is not fully understood and discovery of new enhancers and inhibitors is usually achieved in empirical fashion by trail and error. Although there are reports in literatures concerning the use of luminol-KIO4-H2O2 CL for determination of hydrogen peroxide, glucose and ascorbic acid, the effect of aromatic compounds on luminol-KIO4-H2O2 CL has not been studied systematically. The effects of 36 organic compounds on the luminol-KIO4-H2O2 system chemiluminescence (CL) were studied under different pH conditions of luminol solution The CL signal was detected with flow injection chemiluminescence system (Xi’an Ruimai Electronic Technol. Co.Ltd, China) consisted of model IFFM-D peristaltic pump, mixing tee, model IFFS-A CL detector equipped with glass coil (used as reaction coil and detection cell), photomultiplier, and IBM compatible microcomputer. It was found that most of tested compounds could inhibit or enhance CL intensity. The activities of such inhibitors or enhancers were related to pH value of CL system and number and position of functional groups such as -OH and -NH2 on aromatic ring and property of substituent group, electron delocalization and steric hindrance. The CL spectra and UV-visible absorption spectra were studied and mechanism for CL inhibition and enhancement was also discussed. The mechanism for such inhibition or enhancement of organic compounds is most likely due to the reactions between inhibitors or enhancers and radical intermediates of CL reactions. The possibility of anal. applications was explored based on CL inhibition or enhancement. The results demonstrated that numerous compounds are detectable at ng.mL∓1 level. In addition to this study using 4-Butylbenzene-1,2-diol, there are many other studies that have used 4-Butylbenzene-1,2-diol(cas: 2525-05-5Electric Literature of C10H14O2) was used in this study.

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Electric Literature of C10H14O2

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Alcohol – Wikipedia,
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《Influence of temperature variations on the intensities of absorption bands in the infrared spectra of aliphatic compounds》 was published in Spectrochimica Acta in 1957. These research results belong to Dijkstra, G.. Electric Literature of C10H14O2 The article mentions the following:

Marked changes occur in band intensities throughout the spectra of aliphatic long-chain mols. when liquid samples of these are heated to temperatures up to 200°. In all cases the band intensities are reduced with increasing temperatures, the changes being reversible. These reductions vary considerably from one band to another. The fatty acid dimers form an exception, which, however, can be readily explained. In these substances the C:O stretching band at 1715 cm.-1 gradually disappears on heating, and is replaced by the C:O stretching band of the monomers at 1765 cm.-1 In the experiment, the researchers used many compounds, for example, 4-Butylbenzene-1,2-diol(cas: 2525-05-5Electric Literature of C10H14O2)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Electric Literature of C10H14O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

The author of 《Flotation of antimony oxide》 were Thrun, Eberhard. And the article was published in Chemiker-Zeitung in 1959. HPLC of Formula: 2525-05-5 The author mentioned the following in the article:

The flotation of Sb2O3 ore is discussed theoretically on the basis of chem., phys.-chem., and unit-process parameters. Without resorting to the trial and error approach, it was possible to establish the optimal conditions under which certain dihydroxybutylbenzenes are most effective for the flotation of Sb2O3. The small affinity of the collector at the ore interface was overcome by the simultaneous use of a nonspecific cation-active compound As flotation agents 10 mg. 1,2-dihydroxy-4-butylbenzene/l. and its isomers were used. For the larger-scale flotation experiments, a synthetic mixture was prepared consisting of Sb metal (pretreated Sb2O3) 3.0, SiO2 60.0, CaCO3 17.2, Al2O3 10.3, Fe2O3 5.0%. Other experiments were carried out with the lower Sb contents of 0.8 and 0.24%. After reading the article, we found that the author used 4-Butylbenzene-1,2-diol(cas: 2525-05-5HPLC of Formula: 2525-05-5)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.HPLC of Formula: 2525-05-5 Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

《Hydroxylation of benzene with hydrogen peroxide by the use of hydrophobic catechols and iron(3+) ion complexes as the catalyst》 was published in Chemistry Letters in 1981. These research results belong to Hotta, Kazuhiko; Tamagaki, Seizo; Suzuki, Yusuke; Tagaki, Waichiro. Synthetic Route of C10H14O2 The article mentions the following:

Hydroxylation of C6H6 with H2O2 was carried out in the presence of 3,4-( HO)2C6H3R (I; R = e.g., Me, Et, H, Bu, hexyl) and Fe3+ in a C6H6-H2O biphase system. The hydrophobic catechols I (R = Bu, hexyl, benzyl, PhCH2CH2) were far more effective as the catalyst than the hydrophilic ones.4-Butylbenzene-1,2-diol(cas: 2525-05-5Synthetic Route of C10H14O2) was used in this study.

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.Synthetic Route of C10H14O2 Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Product Details of 2525-05-5On March 31, 1979, Hulisz, Stanislaw; Wawek, Janina published an article in Przemysl Chemiczny. The article was 《Study on the effectiveness of inhibiting furfural autoxidation》. The article mentions the following:

Furfural autoxidation was inhibited by adding 0.01 weight% p-HOC6H4NH2, N(CH2CH2OH)3, 3,4-(HO)2C6H3Bu, HCONH2 or p-(HO)2C6H4. The effectiveness of the additives decreased in the stated order of compounds; the 1st 3 are recommended. The experimental part of the paper was very detailed, including the reaction process of 4-Butylbenzene-1,2-diol(cas: 2525-05-5Product Details of 2525-05-5)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Product Details of 2525-05-5

Referemce:
Alcohol – Wikipedia,
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《Gel chromatographic behavior of mononuclear aromatic hydrocarbons and phenols》 was published in Journal of Chromatography in 1974. These research results belong to Coupek, Jiri; Pokorny, Svatopluk; Pospisil, Jan. Name: 4-Butylbenzene-1,2-diol The article mentions the following:

The gel chromatog. behavior of aromatic hydrocarbons and phenols during elution with THF in columns packed with styrene-divinylbenzene copolymer was investigated. From the elution volumes of 27 aromatic hydrocarbons and 80 phenols, conclusions were drawn about the effects of the types and positions of substituents and of the numbers and positions of phenolic hydroxyl groups on the elution volumes of these compounds in the system under investigation. The effects of the size of the alkyl substituents and of their positions with respect to the hydroxyl group of phenols were determined, and the partial contributions of the alkyl and hydroxyl groups to the elution volumes were calculated Chromatog. results were used for the characterization of the solvatability of phenolic mols. with THF and as the basis of a discussion of problems of the steric hindrance of hydroxyl groups due to neighboring substituents. In addition to this study using 4-Butylbenzene-1,2-diol, there are many other studies that have used 4-Butylbenzene-1,2-diol(cas: 2525-05-5Name: 4-Butylbenzene-1,2-diol) was used in this study.

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.Name: 4-Butylbenzene-1,2-diol Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In 2013,Green and Sustainable Chemistry included an article by Liu, Yi; Sugimoto, Ryuichi; Sumi, Katsuhiro. Name: 4-Butylbenzene-1,2-diol. The article was titled 《Di(isothiocyanato)bis(4-methyl-4′-vinyl-2,2′-bipyridine) ruthenium(II) films deposited on titanium oxide-coated, fluorine-doped tin oxide for an efficient solar cell》. The information in the text is summarized as follows:

Dye-sensitized titanium oxide electrodes were prepared by immobilizing a novel ruthenium complex, di(isothiocyanato) bis(4-methyl-4′-vinyl-2,2′-bipyridine)ruthenium(II) [(NCS)2(mvbpy)2Ru(II)] or the ruthenium complex/sodium 4-vinylbenzenesulfonate onto the surface of a titanium oxide-coated, fluorine-doped tin oxide (TiO2/FTO) electrode through a new electrochem. initiated film formation method, in which the electrolysis step and the film deposition step were individually performed. The incident photon-to-current conversion efficiency (IPCE) of the Ru complex film on a TiO2/FTO electrode was disappointedly insufficient (1.2% at 440 nm). In sharp contrast, the Ru(II) complex/sodium 4-vinylbenzenesulfonate composite film deposited on the surface of a TiO2/FTO electrode showed maximum IPCE of 31.7% at 438 nm. In the experimental materials used by the author, we found 4-Butylbenzene-1,2-diol(cas: 2525-05-5Name: 4-Butylbenzene-1,2-diol)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry.Name: 4-Butylbenzene-1,2-diol Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts