Pea High Quality Nutritional Ingredient Palmitoylethanolamide CAS 544-31-0

• Customization: Available
• Function: Vitamins and Minerals Deficiency Drug, Nutritional Therapeutics
• Certification: GMP
• Model NO.: 99%
• Grade Standard: USP
• Type: Analysis reagent
• State: Powder
• Volatile: Not Volatile
• CAS: 544-31-0
• Transport Package: 25kg
• Specification: 99%
• Trademark: langyue
• Origin: Hunan
• HS Code: 2901
• Production Capacity: 30 Tons/Year

Product Description

Product Name:	Palmitoylethanolamide
Synonyms:	N-(2-HYDROXYETHYL)HEXADECANAMIDE;N-HEXADECANOYLETHANOLAMINE;PEA PALMIDROL;PALMITYLETHANOLAMIDE;PALMITOYLETHANOLAMIDE;PALMITOYLETHANOLAMIDE N-(2-HYDROXYETHYL)HEXADECANAMIDE;n-(2-hydroxyethyl)-hexadecanamid;Palmidrol
CAS:	544-31-0
MF:	C18H37NO2
MW:	299.49
EINECS:	208-867-9

Palmitoylethanolamide (PEA) is an endogenous fatty acid amide, and lipid modulator PEA has been studied in in vitro and in vivo systems using exogenously added or dosed compound; there is evidence that it binds to a nuclear receptor, through which it exerts a variety of biological effects, some related to chronic inflammation and pain.
 

ITEM	SPECIFICATION	RESULT	Test Method
Appearance	White powder	Complies	Visual
Identification	Meet requirement	Complies	HPLC&NMR
Melting point	97~100ºC	98.1ºC	CP2015
Loss on drying	≤1.0%	0.3%	CP2015
Residue on ignition	≤0.1%	0.1%	CP2015
Solubility	Soluble in Ethanol, insoluble in water	Complies	CP2015
Mesh size	90% pass 60 mesh	Complies	CP2015
Bulk density	0.3~0.9g/ml	0.47g/ml	CP2015
Chloride(Cl)	≤0.02%	Complies	CP2015
Sulfate(SO4)	≤0.04%	Complies	USP
Solvent residue (Ethyl acetate)	USP standard	Complies	USP
Total Heavy metals	≤10ppm	Complies	Atomic Absorption
Pb	≤1ppm	Complies	Atomic Absorption
Cd	≤1ppm	Complies	Atomic Absorption
As	≤1ppm	Complies	Atomic Absorption
Hg	≤0.1ppm	Complies	Atomic Absorption
Total microbacterial count	≤100CFU/g	Complies	CP2015
Yeast &Mould	≤10CFU/g	Complies	CP2015
Escherichia Coli presence	Negative	Negative	CP2015
Salmonella	Negative	Negative	CP2015
P. aeruginosa	Negative	Negative	CP2015
S. Aureus	Negative	Negative	CP2015
Bile Tolerant Gram Negative Bacteria	Negative	Complies	EP
Clostridium	Negative	Negative	EP
Assay	≥98.0%	98.9%	HPLC
Conclusion	The results conforms with the Enterprise standard

The testing center of our company is equipped with ULTRAVIOLET room, atom room, gas room, high efficiency liquid room, balance room, high temperature room, chemical room, bacteria examination room, stability laboratory, sample room and central laboratory. Coordinated, comprehensive, systematic and standardized testing of all raw materials, production water, intermediates and finished products to ensure that unqualified raw materials are not put into storage. Disqualified intermediates do not flow into the next process. Nonconforming finished products will not be shipped.
Our goal is zero complaints.




We have our own plant base. Weeding by hand, no pesticides or herbicides used. Control quality from the source.




Packaging:
The product is packed in 25kg or 10kg fiber drum.
It should be stored in its original packing or in a suitable sealed container and kept in a clean and dry place. Storage conditions should preferably be a sheltered environment with limited temperature variations and low humidity levels. Direct contact with water or any other liquid will result in product caking. Under normal circumstances, the use of this product will not cause any undue health hazards. Precautions must be taken to prevent solid or liquid product to contact with skin or eyes.

Customization Service
R&D and Production: We specializes in the development of functional materials and has provided a number of development and improvement solutions.
Granular Production: Our granulation and superfine pulverization can improve bulk density to filling capsules and tablets. and increase water solubility.
Blending and Mixing