L-Cystine
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L-Cystine

Amino Acids Nutritional Enhancers
56-89-3
C₆H₁₂N₂O₄S₂
$26.68 ~ $40.02
Food
Free sample from 100g(NF)
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Product Info

What is L-Cystine?

L-Cystine is a stable, non-essential amino acid primarily used as a nutritional supplement and as a dough conditioner in bakery goods to strengthen the gluten structure.

How is L-Cystine made?

Step No. Production Stage Key Action Control Point & Note
1 Raw Material Preparation Select and clean keratin-rich raw materials, typically poultry feathers or human hair. Wash thoroughly to remove dirt and foreign matter. Source and quality of raw material are critical for final purity. Material must be free from harmful contaminants.
2 Acid Hydrolysis Load the cleaned material into a reactor with concentrated hydrochloric acid (HCl). Heat the mixture to break down the keratin protein into its constituent amino acids. Crucial to control acid concentration, temperature (e.g., 105-115°C), and reaction time (e.g., 8-12 hours). Insufficient hydrolysis results in low yield, while excessive conditions can degrade the L-Cystine.
3 Neutralization & Filtration Cool the acidic hydrolysate and neutralize it with a base (e.g., sodium hydroxide or calcium hydroxide). Filter the solution through activated carbon to decolorize it and remove insoluble impurities. Precise pH adjustment is key to beginning the separation process. The efficiency of the filtration and decolorization steps significantly impacts the purity of the intermediate product.
4 Isolation & Crystallization Carefully adjust the pH of the filtrate to the isoelectric point of L-Cystine (approx. 4.8). L-Cystine, being insoluble at this pH, precipitates out of the solution. Cool the solution to promote crystallization. This is a critical precipitation step. Accurate pH control is mandatory for selective isolation. The cooling rate influences crystal size and purity.
5 Purification (Recrystallization) Separate the crude L-Cystine crystals and re-dissolve them in a dilute acid solution. Repeat the neutralization and precipitation process (Step 4) to wash away remaining soluble impurities. The number of recrystallization cycles depends on the required final purity. Use of purified or deionized water is essential to avoid introducing new contaminants.
6 Centrifuging & Drying Separate the purified L-Cystine crystals from the liquid using a centrifuge. Wash the crystal cake with purified water. Dry the crystals in a vacuum dryer under controlled temperature. Control of drying temperature and time is vital to achieve the specified moisture content without causing thermal degradation. The centrifuge must be hygienically maintained to prevent cross-contamination.
7 Milling & Sieving Mill the dried crystals to achieve a uniform, fine powder. Sieve the powder through a specific mesh to ensure it meets particle size specifications. The mesh size of the sieve is a key control point for ensuring final product consistency and meeting customer requirements for particle size distribution.
8 Quality Control & Packaging Conduct final quality tests for purity (assay), heavy metals, microbial content, specific rotation, and other parameters as per pharmacopoeial standards (e.g., USP, EP). Package the final product in sealed, multi-layer bags. Final product must conform to all specifications before release. Packaging must protect the product from moisture, light, and contamination during storage and transport.

Technical Specifications

CAS Number 56-89-3
Chemical Formula C₆H₁₂N₂O₄S₂
Solubility Poorly soluble in water (~0.112 g/L at 25 °C), soluble in acid/alkali
Storage Conditions Cool, dry, dark; avoid moisture and oxidation
Shelf Life 24 Months

Applications & Usage

Common Applications:

Flour treatment
nutritional supplements
pharmaceuticals
cosmetics
cell culture media

Mechanism of action:

Parameter L-Cystine
Functional Category Dough Conditioner; Flour Treatment Agent; Reducing Agent
Key Ingredients L-Cystine (a dimeric, sulfur-containing amino acid). Often used as its more soluble derivative, L-Cysteine hydrochloride.
Mechanism of Action Functions as a reducing agent in dough systems. The L-Cysteine form cleaves disulfide bonds (S-S) within the gluten protein matrix via a sulfhydryl-disulfide interchange reaction. This breaks down the complex gluten network, reducing its elasticity and increasing its extensibility.
Application Effect in Product Reduces dough mixing time and energy requirements. Improves dough machinability and handling properties (less "bucky"). Increases pan flow for more uniform loaf shape. Results in a softer crumb, finer texture, and potentially increased final product volume.


Comparison:

Product Name Category/Type Key Features Strengths (vs peers) Weaknesses (vs peers) Best Use Cases Why Choose
L-Cystine Dimeric Amino Acid A stable, oxidized dimer of two L-cysteine molecules; a key component of keratin. More chemically stable and less prone to oxidation than L-cysteine. Directly provides a structural unit for hair and nails. Less soluble and potentially has lower bioavailability than NAC or L-cysteine. Does not directly replenish glutathione as effectively as NAC. Long-term structural support for hair, skin, and nails. Providing a stable form of a key keratin building block. For a direct, stable building block to specifically strengthen keratin structures like hair and nails.
N-Acetylcysteine (NAC) Amino Acid Derivative An acetylated form of L-cysteine; a powerful antioxidant and precursor to glutathione. Superior bioavailability; potent antioxidant and mucolytic properties; effectively increases glutathione levels. Primarily functions as an antioxidant and detoxifier, not a direct structural component. Can have a strong sulfur odor. Boosting antioxidant levels, supporting liver health and detoxification, promoting respiratory health by thinning mucus. When the primary goal is potent antioxidant support, liver detoxification, or respiratory benefits, rather than structural protein synthesis.
L-Cysteine Semi-Essential Amino Acid The monomer form of L-cystine; a direct building block for proteins and glutathione. More soluble than L-cystine; a more direct precursor for various metabolic functions beyond structure. Less stable than L-cystine and can be easily oxidized in the digestive system before absorption. General amino acid supplementation for protein synthesis; industrial use as a dough conditioner. When a more soluble, fundamental form of the amino acid is desired for general metabolic roles.
L-Methionine Essential Amino Acid An essential, sulfur-containing amino acid that the body can convert into L-cysteine. As an essential amino acid, it corrects dietary deficiencies that can limit cysteine production. Involved in many critical metabolic pathways. It is an indirect source; conversion to cysteine requires multiple metabolic steps and cofactors. Less targeted than taking cysteine/cystine directly. Addressing dietary insufficiencies of essential sulfur amino acids; supporting overall protein metabolism and methylation cycles. To provide the body with the essential raw material it needs to produce its own cysteine and other sulfur compounds.
Biotin (Vitamin B7) B-Vitamin A water-soluble vitamin that acts as a coenzyme in metabolism, including the synthesis of fatty acids and amino acids. Supports keratin infrastructure through a different metabolic pathway. Very effective for hair and nails if a deficiency exists. Does not provide the physical building blocks for keratin. Benefits are often limited unless correcting a deficiency. Improving hair and nail strength, especially when a biotin deficiency is suspected. Supporting overall energy metabolism. To support the underlying enzymatic processes that build strong hair and nails, rather than supplying the structural components directly.

Technical Documents

Available Documentation

COA, MSDS, technical dossier

Safety Data Sheet (SDS)

Provided

Certificate of Analysis (COA)

Quality assurance documentation

Technical Data Sheet

Detailed technical specifications