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.

Số CAS. 36687-82-8
Công thức phân tử C₁₈H₃₆N₂O₁₂
Trọng lượng phân tử 472.5 g/mol
Hình thức vật lý White Crystals
Ingredient Form L-Carnitine L-Tartrate

Lựa chọn nguyên liệu

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.

Các yếu tố cần xem xét trong quá trình bào chế

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.

Thông số kỹ thuật

L-Carnitine L-Tartrate Technical Specification

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

Test Item Thông số kỹ thuật Result Phương pháp
Identity & Physical Characteristics
Xác định Sample spectrum is consistent with the standard spectrum Conform IR
Hình thức White crystals Conform Hình ảnh
Độ hòa tan Clarification Conform Hình ảnh
Hệ số quay riêng -9.5° to -11.0° -10.46° GB
pH 3.0 to 4.5 3.74 GB
Mất mát khi sấy khô ≤0.5% 0.07% GB
Hàm lượng tro sau khi đốt ≤0.5% 0.08% GB
Thành phần
L-Carnitine 68.2 ± 1.0% 67.93% Titration
L-Tartrate 31.8 ± 1.0% 31.63% Titration
Elemental & Contaminant Controls
Kim loại nặng ≤10 ppm <10 ppm Ch.P
Chì ≤3 ppm <3 ppm AAS
Asen ≤1 ppm <1 ppm Ch.P
Thủy ngân ≤0,1 ppm <0,1 ppm AAS
Cadmium ≤1 ppm <1 ppm AAS
Residue Methanol ≤0.3% <0.3% Ch.P
Cyanide Tiêu cực ND Ch.P
Microbiological Controls
Total Plate Count ≤1000 cfu/g ND Ch.P
Nấm men và nấm mốc ≤100 cfu/g ND Ch.P
E. coli Tiêu cực ND Ch.P
Salmonella Tiêu cực ND Ch.P
Tính chất vật lý
Mật độ khối 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

Ứng dụng

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.

Dinh dưỡng thể thao

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.

Viên nang

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

Máy tính bảng

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

Hỗn hợp bột

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.

Cung ứng thương mại

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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