SU45022A1 - The method of analysis of indaniline obtained from carbazole and n-nitrosophenol - Google Patents

The method of analysis of indaniline obtained from carbazole and n-nitrosophenol

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Publication number
SU45022A1
SU45022A1 SU162302A SU162302A SU45022A1 SU 45022 A1 SU45022 A1 SU 45022A1 SU 162302 A SU162302 A SU 162302A SU 162302 A SU162302 A SU 162302A SU 45022 A1 SU45022 A1 SU 45022A1
Authority
SU
USSR - Soviet Union
Prior art keywords
indaniline
nitrosophenol
carbazole
analysis
alcohol
Prior art date
Application number
SU162302A
Other languages
Russian (ru)
Inventor
А.И. Куликов
Original Assignee
А.И. Куликов
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by А.И. Куликов filed Critical А.И. Куликов
Priority to SU162302A priority Critical patent/SU45022A1/en
Application granted granted Critical
Publication of SU45022A1 publication Critical patent/SU45022A1/en

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  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Description

Лучшие результаты получаютс , если в качестве растворител  примен ть этиловый алкоголь и раствор подкисл ть уксусной кислотой. Реакци  протекает количественно и, почти моментально.Best results are obtained if ethyl alcohol is used as the solvent and the solution is acidified with acetic acid. The reaction proceeds quantitatively and, almost instantly.

Пример. Навеска 0,2-0,3 г инданилина из карбазола и пара-нитрозофенола раствор ют в 100 см алкогол  в колбе Эрленмейера емкостью 0,75 - 1 л при кип чении с обратным холодильником в течение 10 - 15 мин. Прибавл ют 1-2 см 80%-ной уксусной кислоты или соответствующее количество иной концентрации и титруют вначале быстро,Example. A weighed 0.2-0.3 g of indaniline from carbazole and para-nitrosophenol is dissolved in 100 cm of alcohol in a 0.75-1 l Erlenmeyer flask with reflux for 10-15 minutes 1-2 cm of 80% acetic acid or an appropriate amount of a different concentration is added and initially titrated quickly,

(108)(108)

к концу по капл м с выдержкой в 3-5 мин.by the end dropwise with an exposure time of 3-5 minutes.

-2Q- раствором гипосульфита до исчезновени  фиолетовой окраски. Дл  лучшей видимости перехода к концу титровани  прибавл ют 100 см воды.-2Q-hyposulphite solution until the purple color disappears. For better visibility of the transition, 100 cm of water is added to the end of the titration.

Предмет изобретени .The subject matter of the invention.

Способ анализа инданилина, полученного из карбазола и пара-нитрозофенола, отличающийс  тем, что спиртовой раствор инданилина титруют гипосульфитом натри  в присутствии слабой кислоты.A method for analyzing indaniline obtained from carbazole and p-nitrosophenol, wherein the alcohol solution of indaniline is titrated with sodium hyposulfite in the presence of a weak acid.

Тип. .Печатный Труд. Зак. 6194-40аType of. . Printed Labor. Zak 6194-40а

SU162302A 1935-02-04 1935-02-04 The method of analysis of indaniline obtained from carbazole and n-nitrosophenol SU45022A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU162302A SU45022A1 (en) 1935-02-04 1935-02-04 The method of analysis of indaniline obtained from carbazole and n-nitrosophenol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU162302A SU45022A1 (en) 1935-02-04 1935-02-04 The method of analysis of indaniline obtained from carbazole and n-nitrosophenol

Publications (1)

Publication Number Publication Date
SU45022A1 true SU45022A1 (en) 1935-11-30

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Family Applications (1)

Application Number Title Priority Date Filing Date
SU162302A SU45022A1 (en) 1935-02-04 1935-02-04 The method of analysis of indaniline obtained from carbazole and n-nitrosophenol

Country Status (1)

Country Link
SU (1) SU45022A1 (en)

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