Jiangsu Changqing Agrochemical Co.

Changqing, China

Jiangsu Changqing Agrochemical Co.

Changqing, China

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News Article | February 22, 2017
Site: en.prnasia.com

ZHENJIANG, China, Feb. 22, 2017 /PRNewswire/ -- Delta Technology Holdings Limited (NASDAQ: DELT), a manufacturer and seller of specialty chemicals, today announced that it is increasing both the number of core clients it serves and the amount of product sold to these companies. "We are confident that the products we produce for pharmaceutical and pesticide companies, and companies in other sectors including clean energy, food additives, aerospace and agrochemical, allow these major firms to achieve successes. We are very proud of the strategic cooperation these major companies have with Delta Technology," said Chao Xin, Chairman and CEO. Delta Technology services giant international chemical companies including Bayer, BASF Corporation, FMC Corporation as well as several public companies in China listed on the Shenzhen Stock Exchange for example: Jiangsu Flag Chemical Industry Co., Ltd.; Jiangsu Huifeng Agrochemical Co., Ltd., Huapont Life Sciences Co, Ltd. and Jiangsu Changqing Agrochemical Co., Ltd. Founded in 2007, Delta Technology Holdings Ltd. is a leading China-based fine and specialty chemical company producing and distributing organic compound including para-chlorotoluene ("PCT"), ortho-chlorotoluene ("OCT"), PCT/OCT downstream products, unsaturated polyester resin ("UPR"), maleic acid ("MA") and other by-product chemicals. The end application markets of the Company's products include Automotive, Pharmaceutical, Agrochemical, Dye & Pigments, Aerospace, Ceramics, Coating-Printing, Clean Energy and Food Additives. Delta has approximately 300 employees, 25% of whom are highly-qualified experts and technical personnel. The Company serves more than 380 clients in various industries. This press release may contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements are subject to known and unknown risks, uncertainties and other factors that may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Statements preceded or followed by or that otherwise include the words "believes," "expects," "anticipates," "intends," "projects," "estimates," "plans," and similar expressions or future or conditional verbs such as "will", "should", "would", "may" and "could" are generally forward-looking in nature and not historical facts. Forward-looking statements in this release also include statements about business and economic trends. Investors should also consider the areas of risk described under the heading "Forward Looking Statements" and those factors captioned as "Risk Factors" in DELT's periodic reports under the Securities Exchange Act of 1934, as amended, or in connection with any forward-looking statements that may be made by DELT. To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/delta-technology-holdings-limited-continues-to-expand-revenues-from-core-client-base-300411535.html


Wang X.,Yangzhou University | Li Y.,Yangzhou University | Yuan Y.,Yangzhou University | Yuan Y.,Jiangsu Changqing Agrochemical Co.
Synthesis (Germany) | Year: 2013

The copper-catalyzed direct thiolation of benzothiazole with iodobenzene and sulfur in superbase system under oxygen atmosphere is reported. The corresponding 2-thio-substituted benzothiazoles were formed in satisfactory yields. © Georg Thieme Verlag KG Stuttgart · New York.


Han Y.,Yangzhou University | Wang X.,Yangzhou University | Lv L.,Jiangsu Changqing Agrochemical Co. | Diao G.,Yangzhou University | Yuan Y.,Yangzhou University
Synthesis | Year: 2012

The catalytic coupling reaction of aryl halides and heterocycles has been developed using copper powder as the catalyst in N,N-dimethylacetamide. The procedure is experimentally simple and free from the addition of external cocatalysts or chelating ligands. © Georg Thieme Verlag.


Liu S.,Nanjing College of Chemical Technology | Zhu H.-J.,Nanjing University of Technology | Yu G.-Q.,Jiangsu Changqing Agrochemical Co. | Du G.,Jiangsu Changqing Agrochemical Co. | Lv L.-Z.,Jiangsu Changqing Agrochemical Co.
Acta Crystallographica Section E: Structure Reports Online | Year: 2012

In the crystal structure of the title compound, C 5H 8N 2O, molecules are linked by weak C-H⋯O hydrogen bonds, forming a three-dimensional network.

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