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870855A

Avanti

3-Me-Glutaryl Carnitine

Avanti Research™ - A Croda Brand 870855A, paste

Synonym(s):

3-methylglutaryl L-carnitine

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About This Item

Empirical Formula (Hill Notation):
C13H23NO6
CAS Number:
102673-95-0
Molecular Weight:
289.32
UNSPSC Code:
12352211
NACRES:
NA.25

form

paste

packaging

pkg of 1 × 5 mg (870855A-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870855A

lipid type

bioactive lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

C[N+](C)(C)C[C@H](OC(CC(C)CC(O)=O)=O)CC([O-])=O

InChI

1S/C13H23NO6/c1-9(5-11(15)16)6-13(19)20-10(7-12(17)18)8-14(2,3)4/h9-10H,5-8H2,1-4H3,(H-,15,16,17,18)

InChI key

HFCPFJNSBPQJDP-UHFFFAOYSA-N

Biochem/physiol Actions

3-Me-Glutaryl Carnitine metabolite may be found in urine samples. The detection of 3-methylglutarylcarnitine and other metabolites may play a role in a treatment strategy for carnitine deficiency.

Packaging

5 mL Clear Glass Sealed Ampule (870855A-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

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Description
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Storage Class Code

10 - Combustible liquids

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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S Jooste et al.
Clinica chimica acta; international journal of clinical chemistry, 230(1), 1-8 (1994-10-14)
Two patients, diagnosed with 3-methylglutaconic aciduria, who presented with diverse clinical and metabolic manifestations, were studied. Glycine conjugation as a possible detoxification mechanism in these two patients yielded negative results. Carnitine conjugates were however detected. 3-Methylglutarylcarnitine was observed in the
C R Roe et al.
The Journal of clinical investigation, 77(4), 1391-1394 (1986-04-01)
Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A (CoA) lyase affects the metabolism of leucine as well as ketogenesis. This disorder is one of an increasing list of inborn errors of metabolism that presents clinically like Reye's Syndrome or nonketotic hypoglycemia. Four patients with

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