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93544

Supelco

N-Hexanoylglycine

analytical standard

Synonym(s):

2-(Hexanoylamino)acetic acid, N-(1-Oxohexyl)glycine, N-Caproylglycine, Hexanoyl glycine, NSC 224460

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About This Item

Empirical Formula (Hill Notation):
C8H15NO3
CAS Number:
Molecular Weight:
173.21
Beilstein:
1773416
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

clinical testing

format

neat

storage temp.

2-8°C

InChI

1S/C8H15NO3/c1-2-3-4-5-7(10)9-6-8(11)12/h2-6H2,1H3,(H,9,10)(H,11,12)

InChI key

UPCKIPHSXMXJOX-UHFFFAOYSA-N

Biochem/physiol Actions

Hexanoylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction:acyl-CoA + glycine ↔CoA + N-acylglycine. Hexanoylglycine is a fatty acid metabolite, it appears in the urine of patients with hereditary medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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P Rinaldo et al.
Biomedical & environmental mass spectrometry, 18(7), 471-477 (1989-07-01)
We describe a gas chromatographic/mass spectrometric method for the accurate determination of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in urine for the diagnosis of hereditary medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. These acylglycines had previously been detected in urine from patients with MCAD

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