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Lignin

Lignin Structure
CAS No.
9005-53-2
Chemical Name:
Lignin
Synonyms
LIGNIN;C05615;LIGNINE;PHYLLANTIN;Ligrion, GR;LIGNIN,ALKALINE;PURIFIED LIGNIN;LIGNINE ALKALINE;LIGNIN,DEALKALINE;LIGNINE USP/EP/BP
CBNumber:
CB5255412
Molecular Formula:
unspecified
Molecular Weight:
0
MOL File:
Mol file
Modify Date:
2024/12/18 14:08:57

Lignin Properties

storage temp. Store at -20°C
solubility DMSO : ≥ 50 mg/mL;Water : < 0.1 mg/mL (insoluble)
form Solid
color Brown to black
Merck 14,5487
Stability Stable. Incompatible with strong oxidizing agents.
EPA Substance Registry System Lignin (9005-53-2)

SAFETY

Risk and Safety Statements

HS Code  39072090

Lignin price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ottokemi L 1457 Ligrion, GR 9005-53-2 500mL ₹1971 2022-05-26 Buy
Product number Packaging Price Buy
L 1457 500mL ₹1971 Buy

Lignin Chemical Properties,Uses,Production

Description

An abundant phenylpropane polymer found in all vascular plants. Lignin acts as the "glue" for cellulose and hemicellulose constit uents of plants, and the three substances comprise the major cell wall components of cellulosic plants, e.g., woody and grassy plants. These substances are bound tightly and may only be sep arated under vigorous conditions. Lignin finds use as a drilling fluid additive, asphalt emulsion stabilizer, protein precipitant, rub ber strengthener and precursor for the synthesis of phenol, vanillin and other products.

Chemical Properties

The term "lignin" is derived from the Latin lignum for wood, and woody plants or parts of plants contain large quantities of this substance. lignin is an irnportant skeletal component of secondary cell walls and is thus not found in young plants or parts of plants that are still growing. It is lignin that provides the hardness and rigidity of tree trunks and the sterns of perennial plants. In the cell wall, lignin is bound to other components, notably hemicelluloses. The lignin-cellulose-hemicellulose complex has economic irnportance in the production of paper from wood. The strong bonds linking cellulosic material to lignin render the former inaccessible to enzyme hydrolysis, and thus lignin has a direct influence on the digestibility, and hence the nutritive value, of herbage plants to grazing animals. In herbage plants, lignin is also bonded to cell wall protein.
Lignification of plants affects the palatability of fruits and vegetables. Thus, the unpleasant "stone cells" in pears are due to lignification, and many root and stern crops, such as carrots, beetroot, celery or asparagus, when old become inedible through lignification.

Occurrence

Lignin is a 3-dimensional type of polymer of phenol elements with heavy-duty intermolecular bonding by strongly divided molecules. The main sources of lignins are coniferyl, p-coumaryl and sinapyl alcohols[1]. The intensity of lignin in wheat stems and roots is 4.4 and 5.6, which is considerably stronger (p < 0.001) than in wheat leaves. Lignin differs in composition between species. For example, the composition of the aspen specimen is 5.9% hydrogen, 63.4% carbon, 0.7% ash (mineral components), and 30% oxygen (by difference), conforming to the formula (C31H34O11)n.

Uses

Source of vanillin, syringic aldehyde, dimethyl sulfoxide, Lignin (Dealkaline) can be extender for phenolic plastics, to strengthen rubber (esp for shoe soles), as oil mud additive, to stabilize asphalt emulsions, to precipitate proteins.

Biosynthesis

Lignin biosynthesis is a very complex network that is divided into three processes: (i) biosynthesis of lignin monomers, (ii) transport, and (iii) polymerization. After a series of steps involving deamination, hydroxylation, methylation, and reduction, lignin monomers are produced in the cytoplasm and transported to the apoplast. Finally, lignin is generally polymerized with three main types of monolignols (sinapyl alcohol, S unit; coniferyl alcohol, G unit and p-coumaryl alcohol, H unit) by peroxidase (POD) and laccase (LAC) in the secondary cell wall. In addition, several other compounds, including hydroxycinnamaldehydes, tricin flavones, hydroxystilbenes xenobiotics, etc., have also been recognized as lignin subunits [2].

Agricultural Uses

The overall appearance of lichens is described as crustose (they make a thin and flat crust on the substratum), foliose or fruticose (upright, branched forms, resembling shrubs). Lichens grow slowly from a few millimeters to several meters each year. They reproduce mostly by the development of apothecia or perithecia, forming new lichens on germination of the ascospores only in the presence of the algal partner in whose absence the fungus dies.
Nearly 700 chemicals, which are unique to lichens, help lichens to survive and ward off attacks by bacteria, other fungi and grazing herbivores.
Lichens belong to soil-crust communities and help stabilize soils, especially in desert areas. Cyanolichens contribute to fixing nitrogen to the ecosystem in which they grow. LicheGare used for identifying the age of the surface (on which they grow) by a technique, called lichenometry..
Lichens are pollution indicators because of their differential sensitivity to sulphur dioxide (SO2), nitrogen dioxide (NO2) and ozone, as well as their ability to absorb and accumulate heavy metals and radionuclides..
Substances like pigments, toxins, antibiotics, etc. are obtained from lichens, which are especially useful as a source of dyes (for example, Roccella, providing litmus), medicines and perfumes. Some lichens, like Iceland moss and reindeer moss, are used as food in arctic regions.

References

[1] Muhammad Waheed Riaz. “Role of Lignin in Wheat Plant for the Enhancement of Resistance against Lodging and Biotic and Abiotic Stresses.” Journal of Thermal Stresses 60 1 (2023).
[2] Qingquan Liu, Luqing Zheng, Le Luo. “Lignins: Biosynthesis and Biological Functions in Plants.” International Journal of Molecular Sciences 19 2 (2018).

Lignin Preparation Products And Raw materials

Global( 137)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Otto Chemie Pvt. Ltd. +91 9820041841 Mumbai, India 5870 58 Inquiry
NAMOH SALES INDIA PVT LTD 08048372614Ext 465 Delhi, India 1 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6768 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20235 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21628 55 Inquiry
Shaanxi Pioneer Biotech Co., Ltd . +8613259417953 China 1287 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29808 58 Inquiry
Zhengzhou Alfa Chemical Co.,Ltd +8618530059196 China 12162 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 32159 58 Inquiry
Hubei Ipure Biology Co., Ltd +8613367258412 China 10244 58 Inquiry
PHYLLANTIN LIGNINE ALKALINE LIGNIN LIGNIN,ALKALINE LIGNIN,DEALKALINE LIGNINE 3,4-DICHLOROANILINE-LIGNINMETABOLITE LIGNINE, DEALKALINE C05615 Lignine (80%) Dealkaline Lignin (Alkaline),RG LIGNINE USP/EP/BP Ligrion, GR PURIFIED LIGNIN Lignin (Dealkaline) (technical grade) 9005-53-2 Miscellaneous Natural Products Elisa Kit-plant ELISA Kit