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Stable Isotopes Product Detail
Home Stable Isotopes CS-T-96940

Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride

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Product Code: CS-T-96940 Stable Isotopes Research Use Only
Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride
Category
Stable Isotopes
API Family
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Product Code
CS-T-96940
Research Status
For Laboratory Use

Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride

Stable Isotopes
Stock Status: : Enquire Live

CAT No.
CS-T-96940
CAS No.
42150-38-9(Unlabelled)
Molecular Formula
C23H41D3ClNO6
Molecular Weight
469.07
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal or Veterinary use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
42150-38-9(Unlabelled)
Product Code
CS-T-96940
M.F.
C23H41D3ClNO6
M.W.
469.07
Smiles
OC(CCCCCCCCCCCCCCC(O[C@H](CC([O-])=O)C[N+](C)(C([2H])([2H])[2H])C)=O)=O
Category
Stable Isotopes
Storage Condition
Refer MSDS for complete information.
IUPAC Name
Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride
References
"Millington, D.S., Stevens, R.D.: Method Mol. Bio., 708, 55 (2011)"
Synonyms
"(R)-3-Carboxy-2-[(15-carboxy-1-oxopentadecyl)oxy]-N,N,N-trimethyl-d3-1-propanaminium Chloride; (R)-3-((15-Carboxypentadecanoyl)oxy)-4-(trimethyl-d3-ammonio)butanoate Chloride"
Application Notes
"Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride is the labeled analogue of Hexadecanedioic Acid Mono-L-carnitine Ester (H290970), a fatty acid metabolite used in diagnostic test for inherited disorders of fatty acid and branched-chain amino acid catabolism."
Hazard Compound
Refer MSDS for complete information.
Overview
"Hexadecanedioic Acid Mono-L-carnitine-d3 Ester Chloride is the labeled analogue of Hexadecanedioic Acid Mono-L-carnitine Ester (H290970), a fatty acid metabolite used in diagnostic test for inherited disorders of fatty acid and branched-chain amino acid catabolism."

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