Joint Health Ingredient

MSM Powder Supplier | Methylsulfonylmethane

Methylsulfonylmethane (MSM) supplied as a crystalline ingredient for supplement formulations, with batch-level analytical results available for specification review.

MSM PRODUCT IMAGE

Product Information

MSM at a Glance

Core identity and product reference information.

No CAS 67-71-0
Formule moléculaire C₂H₆O₂S
Poids moléculaire 94.14 g/mol
Forme physique White powder or crystals
Test Standard USP42

Product Overview

Methylsulfonylmethane for Formulation

MSM is supplied as a crystalline ingredient. Product qualification should be based on the required identity, analytical specification and intended formulation.

What to Confirm Before Ordering

Review the specification against your formulation and market requirements before moving to a bulk order.

Identité des ingrédients Confirm the material and required analytical identity for your formula.
Spécifications Check assay, purity, physical properties and impurity limits.
Taille des particules Confirm the required particle size for your processing and dosage form.
Documentation Review the applicable COA and supporting product information.

Batch Evidence

The supplied Certificate of Analysis records the tested batch number, production information, analytical methods and measured results rather than relying only on a general product specification.

Product Batch

MSM Batch Information

Reference details from the supplied Certificate of Analysis.

Produit Méthylsulfonylméthane (MSM)
Batch No. 20250212
Batch Size 100 kg
Manufacture Date 2025-02-12
Date d'expiration 2027-02-11

Caractéristiques techniques

MSM Specification & COA Results

Analytical requirements, methods and batch results from the supplied certificate.

Test Item Spécifications Test Method Result
Chemical & Physical Properties
Dosage 98.0–102.0% USP42<621> 99.96%
Chromatographic Purity ≥99.9% 99.92%
DMSO Content ≤0.01% USP42<621> Négatif
Apparence White powder or crystals Crystals
Odeur Sans odeur Sans odeur
Identification Passes test IR/HPLC Passes test
Point de fusion 108.5–110.5°C USP42<741> 108.6°C
Densité en vrac ≥0.70 g/ml 0.74 g/ml
Teneur en eau ≤0.10% USP42<921> 0.09%
Any Other Individual Impurity ≤0.05% 0.03%
Total Impurities ≤0.20% 0.06%
Résidus à l'allumage ≤0.10% USP42<281> 0.01%
pH Value ≤7 pH meter 4.1
Solvants résiduels
Solvants résiduels Complies with EU GC Complies
Methanol NMT 3000 ppm GC ND
Ethanol NMT 5000 ppm GC ND
Acetone NMT 5000 ppm GC ND
Isopropanol NMT 5000 ppm GC ND
Métaux lourds
Heavy Metals (as Pb) ≤3 ppm USP42<231> <3 ppm
Plomb (Pb) < 0,1 ppm USP42<231> < 0,1 ppm
Arsenic (As) < 0,1 ppm USP42<231> < 0,1 ppm
Cadmium (Cd) < 0,1 ppm USP42<231> < 0,1 ppm
Mercure (Hg) < 0,1 ppm USP42<231> < 0,1 ppm
Microbiological Testing
Coliform Négatif USP42<2022> Négatif
E. coli Négatif USP42<2021> Négatif
Yeast / Mold <10 CFU/g USP42<2021> <10 CFU/g
Salmonelle Négatif USP42<2021> Négatif
Standard Aerobic Plate Count <10 CFU/g USP42<2021> <10 CFU/g
Total Plate Count <1000 CFU/g USP42<2021> <1000 CFU/g
Taille des particules
Taille des particules 100 mesh Conform
COA Conclusion

The supplied certificate states that the product conforms to the enterprise standard.

Solubilité

The supplied certificate states 100% water soluble.

Application Areas

MSM in Supplement Formulations

MSM is used as an ingredient in formulations where methylsulfonylmethane is specified, including joint-health and active-nutrition products.

01

Joint Health Formulas

Used as an ingredient in joint-health formulations and combination products.

02

Capsules et comprimés

Used in dry dosage forms where the required MSM specification and particle size are defined.

03

Powder Drinks & Sachets

Can be considered for water-based powder formulations where solubility and particle size are evaluated.

04

Nutrition active

Used in sports and active-nutrition formulations alongside other selected ingredients.

Product Documentation

Documentation for Specification Review

Information used to evaluate the product before formulation or purchase.

Certificate of Analysis

Batch-level analytical data covering identity, assay, physical properties, impurities, residual solvents, heavy metals and microbiological testing.

Caractéristiques techniques

Defined analytical limits can be compared with the requirements of your formulation and applicable market specifications.

Product Qualification

Share your target specification and application so the required product parameters can be reviewed before quotation.

Emballage

Packaging & Batch Reference

Packaging and batch details recorded in the supplied certificate.

25 KG / Drum

The supplied COA records a packing size of 25 kg per drum and a drum quantity of 4 for the referenced batch.

Expiration

The referenced batch has an expiration date of 2027-02-11.

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