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Merck
CN

92855

Glycerol trienanthate

≥94%

Synonym(s):

1,2,3-Trienanthoylglycerol, Glycerol triheptanoate, Triheptanoin, Trioenanthin

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About This Item

Linear Formula:
[CH3(CH2)5COOCH2]2CHOCO(CH2)5CH3
CAS Number:
620-67-7
Molecular Weight:
428.60
EC Number:
210-647-2
UNSPSC Code:
12352100
PubChem Substance ID:
57653497
Beilstein/REAXYS Number:
1807724
MDL number:
MFCD00042910

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Product Name

Glycerol trienanthate, ≥94%

InChI key

PJHKBYALYHRYSK-UHFFFAOYSA-N

InChI

1S/C24H44O6/c1-4-7-10-13-16-22(25)28-19-21(30-24(27)18-15-12-9-6-3)20-29-23(26)17-14-11-8-5-2/h21H,4-20H2,1-3H3

SMILES string

CCCCCCC(OCC(COC(CCCCCC)=O)OC(CCCCCC)=O)=O

assay

≥94% (TLC)
≥94%

form

liquid

refractive index

n20/D 1.444

density

0.966 g/mL at 20 °C (lit.)

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

404.6 °F - open cup

flash_point_c

207 °C - open cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
1414231V
1414231
261979/1
275960/1

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Sophie Calvert et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 22(6), 1074-1080 (2018-08-22)
Despite antiepileptic medication and dietary treatment options available about 45% of children with epilepsy still suffer from uncontrolled seizures. Triheptanoin is an anaplerotic treatment designed to improve energy generation via the Krebs cycle. For the first time, we evaluated the
Mohan Gomathi et al.
Journal of autism and developmental disorders, 50(8), 2740-2764 (2020-02-06)
Drug studies on Rett syndrome (RTT) have drastically increased over the past few decades. This review aims to provide master data on bench-to-bedside drug studies involving RTT. A comprehensive literature review was performed by searching in PUBMED, MEDLINE and Google
Keri J Fogle et al.
Molecular genetics and metabolism, 126(4), 439-447 (2019-01-27)
Seizures are a feature not only of the many forms of epilepsy, but also of global metabolic diseases such as mitochondrial encephalomyopathy (ME) and glycolytic enzymopathy (GE). Modern anti-epileptic drugs (AEDs) are successful in many cases, but some patients are
Juan M Pascual et al.
JAMA neurology, 71(10), 1255-1265 (2014-08-12)
Disorders of brain metabolism are multiform in their mechanisms and manifestations, many of which remain insufficiently understood and are thus similarly treated. Glucose transporter type I deficiency (G1D) is commonly associated with seizures and with electrographic spike-waves. The G1D syndrome
Cory J White et al.
Molecular and cellular biology, 40(10) (2020-03-04)
The metabolic state of the brain can greatly impact neurologic function. Evidence of this includes the therapeutic benefit of a ketogenic diet in neurologic diseases, including epilepsy. However, brain lipid bioenergetics remain largely uncharacterized. The existence, capacity, and relevance of
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