According to a new market report published by Credence Research Inc., Hematoxylin Market by Application (Laboratories & Textile), by Type (Alum Hematoxylin, Iron Hematoxylin, Tungsten Hematoxylin & Others)  - Growth, Future Prospects, Competitive Analysis and Forecast, 2017 2025, the worldwide hematoxylin market was valued at US$ 1,532.64 Mn in 2016. 

Browse the full report at http://www.credenceresearch.com/report/hematoxylin-market

Market Insights:

Hematoxylin market is projected to witness high growth owing to rising demand from end use application. It is widely use as dye in histological studies and textiles application. Furthermore, aging global population, growing number of diseases and standardization of pathological laboratories are the factors anticipated to drive the investment in research and development with the concentration to cure the critical diseases such as cancer, etc. Increasing research and development in biomedical is fueling the demand for dyes such as hematoxylin.

However, volatile raw material prices & increasing use of substitutes are the factors hampering the market growth. China, Japan and India are expected to be the most attractive markets for hematoxylin, offering high growth potential. Besides this, Asia Pacific offers low cost of manufacturing, which can provide competitive advantage to the hematoxylin.

Competitive Insights:

The global market for hematoxylin is highly competitive and fragmented due to presence of various players. To gain competitive advantage, players should provide better services to buyers. Market players are involved in adopting various strategies such as geographical expansion, mergers, acquisitions, and R & D (Research & Development) in order to develop their business and survive in the long run. Some of the prominent players present in this market are Abbey Color, Sigma-Aldrich, Thermo Fisher Scientific, Inc., American MasterTech Scientific Incorporated, Cardinal Health, Inc. and Molychem among others.

Key Trends:

• Asia Pacific offers huge untapped market potential
• Rising demand from end use application

Growing prevalence of various disease along with rising demand for personalized medicine is projected to propel the demand for hematoxylin over the forecast period

 Browse the full report at http://www.credenceresearch.com/report/hematoxylin-market

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Haematoxylin or hematoxylin (/himtksln/), also called natural black 1 or C.I. 75290, is a compound extracted from the heartwood of the logwood tree (Haematoxylum campechianum).[1] Haematoxylin and eosin together make up haematoxylin and eosin stain, one of the most commonly used stains in histology. This type of stain is a permanent stain as opposed to temporary stains (e.g. iodine solution in KI). Another common stain is phosphotungstic acid haematoxylin, a mix of haematoxylin with phosphotungstic acid. When oxidized, it forms haematein, a compound that forms strongly coloured complexes with certain metal ions, the most notable ones being Fe(III) and Al(III) salts. Metal-haematein complexes are used to stain cell nuclei prior to examination under a microscope. Structures that stain with iron- or aluminium-haematein are often called basophilic, even though the mechanism of the staining is different from that of staining with basic dyes.

In the early 1970s and in 2008, there were shortages of haematoxylin due to interruptions in its extraction from logwood. The price of the compound increased, affecting the cost of diagnostic histopathology, and prompted a search for alternative nuclear stains. Before the use of any alternatives became firmly established, haematoxylin returned to the market, though at a higher price, and resumed its place in histopathology. Several synthetic dyes have been recommended as replacements, notably celestine blue (CI 51050), gallocyanine (CI 51030), gallein (CI 45445) and eriochrome cyanine R (also called chromoxane cyanine R and solochrome cyanine (CI 43820). All four have Fe(III) as the mordant. Another alternative is the aluminium complex of oxidized brazilin, which differs from haematoxylin by only one hydroxyl group. Source: Wikipedia

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