L-Carnitine L-Tartrate Ingredient

L-Carnitine L-Tartrate Powder Manufacturer & Supplier

L-Carnitine L-Tartrate powder is supplied for nutritional and sports-nutrition formulations requiring this specific carnitine form, with analytical specifications and product documentation available for ingredient qualification and commercial purchasing.

L-Carnitine L-Tartrate powder bulk ingredient

Product Information

L-Carnitine L-Tartrate Powder

Chemical and physical identifiers for specifying the correct L-Carnitine L-Tartrate raw material.

CAS番号. 36687-82-8
分子式 C₁₈H₃₆N₂O₁₂
分子量 472.5 g/mol
物理的な形態 White Crystals
成分の形態 L-カルニチン L-酒石酸塩

食材の選択

L-Carnitine L-Tartrate for Formulation

L-Carnitine L-Tartrate combines L-Carnitine with L-tartaric acid in a defined salt form. Ingredient selection should therefore be based on the specific carnitine form required by the formulation.

Selecting the Correct L-Carnitine Form

L-Carnitine L-Tartrate should be specified by its complete ingredient name when sourcing material for a formulation. L-Carnitine base, L-Carnitine L-Tartrate and other carnitine forms have different composition profiles and should be evaluated against the formulation and purchasing specification separately.

製剤に関する考慮事項

Review the ingredient form together with the intended dosage format, target L-Carnitine contribution and manufacturing process. For dry blends, capsules and tablets, physical properties such as particle size and density may also be relevant during formulation trials and scale-up.

技術仕様

L-Carnitine L-Tartrate Technical Specification

Analytical criteria covering identity, composition, physical characteristics, contaminants and microbiological quality.

Test Item 仕様 Result 方法
Identity & Physical Characteristics
識別 Sample spectrum is consistent with the standard spectrum Conform IR
外観 White crystals Conform ビジュアル
溶解度 Clarification Conform ビジュアル
特定のローテーション -9.5° to -11.0° -10.46° GB
pH 3.0 to 4.5 3.74 GB
乾燥減量 ≤0.5% 0.07% GB
点火時の残留物 ≤0.5% 0.08% GB
構成
L-カルニチン 68.2 ± 1.0% 67.93% Titration
L-Tartrate 31.8 ± 1.0% 31.63% Titration
Elemental & Contaminant Controls
重金属 ≤10 ppm <10 ppm Ch.P
リード ≤3 ppm <3 ppm AAS
ヒ素 ≤1 ppm <1 ppm Ch.P
水星 ≤0.1 ppm <0.1 ppm AAS
カドミウム ≤1 ppm <1 ppm AAS
Residue Methanol ≤0.3% <0.3% Ch.P
Cyanide 否定 ND Ch.P
Microbiological Controls
Total Plate Count ≤1000 cfu/g ND Ch.P
酵母とカビ ≤100 cfu/g ND Ch.P
大腸菌 否定 ND Ch.P
サルモネラ菌 否定 ND Ch.P
物理的性質
かさ密度 0.4–0.8 g/ml Conform Physical
Tap Density 0.5–0.9 g/ml Conform Physical
Mesh Through 12 mesh 100% passed 12 mesh screen

アプリケーション

Applications for L-Carnitine L-Tartrate Powder

The ingredient can be evaluated across nutritional formats where L-Carnitine L-Tartrate is the specified carnitine form.

スポーツ栄養学

Suitable for sports-nutrition concepts that specify L-Carnitine L-Tartrate as the carnitine source. Target active contribution should be calculated from the ingredient composition.

カプセル

For capsule development, evaluate the required ingredient loading together with capsule size, excipients and the physical behavior of the complete blend.

タブレット

Tablet projects should consider ingredient loading, blend behavior and processing requirements during formulation trials before commercial scale-up.

パウダーブレンド

In dry formulations, evaluate distribution and handling with the actual carrier system and other ingredients used in the finished product.

Ingredient Qualification

Qualifying L-Carnitine L-Tartrate for Production

Ingredient approval should connect the required carnitine form with formulation performance, documentation and the commercial material intended for production.

Formulation Evaluation

Evaluate the material in the intended dosage form before commercial production, particularly where ingredient loading or powder behavior can affect processing.

Active contribution Calculate the required raw-material addition from the L-Carnitine contribution specified for the formulation.
Processing fit Review the powder in the actual blend and manufacturing process rather than assessing the ingredient in isolation.

Purchasing Qualification

Before moving from sample evaluation to a commercial order, align the approved material with the documentation and purchasing requirements used by your quality and procurement teams.

Approved material Keep the complete ingredient name consistent across internal specifications, purchasing records and supplier documents.
Commercial lot Review the applicable lot documentation before material is released for production use.

業務用供給

Bulk L-Carnitine L-Tartrate Supply

Packaging and documentation can be reviewed as part of commercial purchasing and supplier qualification.

Commercial Packaging

The documented commercial format is suitable for bulk ingredient purchasing. Confirm packaging requirements for the intended order and destination during quotation.

25 KG / BUCKET

Product Documentation

Product documentation can be reviewed during ingredient qualification and before commercial purchasing to support internal quality and procurement procedures.

COA AVAILABLE

Commercial Inquiry

Request L-Carnitine L-Tartrate Pricing

Share your purchasing requirements so the product and commercial information can be matched to your formulation and supply needs.

01

Quantity & Destination

Provide your estimated purchasing quantity and destination country or region.

02

Finished-Product Format

Tell us whether the material is intended for capsules, tablets, powder blends or another nutritional format.

03

Purchasing Requirements

Include any internal qualification conditions or commercial requirements that should be considered with the quotation.

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