agaric acid
Suppliers
Names
[ CAS No. ]:
666-99-9
[ Name ]:
agaric acid
[Synonym ]:
Laricic acid
n-Hexadecylcitric acid
EINECS 211-566-5
Agaricinic acid
(2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure
Lr-2-Hydroxy-nonadecan-1,2rF,3cF-tricarbonsaeure
Agaric acid
Agaricinsaeure
MFCD00002665
Agaricin
(2S,3S)-2-Hydroxy-nonadecan-1,2,3-tricarbonsaeure (Agaricinsaeure)
Agaricic acid
(2S,3S)-2-hydroxy-nonadecane-1,2,3-tricarboxylic acid
Chemical & Physical Properties
[ Density]:
1.115g/cm3
[ Boiling Point ]:
509.3ºC at 760 mmHg
[ Melting Point ]:
142° (dec)
[ Molecular Formula ]:
C22H40O7
[ Molecular Weight ]:
416.54900
[ Flash Point ]:
275.9ºC
[ Exact Mass ]:
416.27700
[ PSA ]:
132.13000
[ LogP ]:
4.84900
[ Index of Refraction ]:
1.501
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- RA5365000
- CHEMICAL NAME :
- 1,2,3-Nonadecanetricarboxylic acid, 2-hydroxy-
- CAS REGISTRY NUMBER :
- 666-99-9
- BEILSTEIN REFERENCE NO. :
- 1729981
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 1
- MOLECULAR FORMULA :
- C22-H40-O7
- MOLECULAR WEIGHT :
- 416.62
- WISWESSER LINE NOTATION :
- QVY16&XQVQ1VQ
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LDLo - Lowest published lethal dose
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - rabbit
- DOSE/DURATION :
- 100 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- HBAMAK "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." (Leipzig, Ger. Dem. Rep.) Volume(issue)/page/year: 4,1289,1935
Safety Information
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
RA5365000
Precursor & DownStream
Precursor
DownStream
Articles
Mitochondrion 5 , 272-281, (2005)
The effect of agaric acid as inducer of mitochondrial permeability transition was studied. It was found that: (i) agaric acid (AA) promoted efflux of accumulated Ca2+, collapse of transmembrane potent...
J. Bioenerg. Biomembr. 31 , 447-455, (1999)
Nonesterified long-chain fatty acids have long been known as uncouplers of oxidative phosphorylation. They are efficient protonophores in the inner mitochondrial membrane but not so in artificial phos...
Cell Biochem. Biophys. 51 , 81-87, (2008)
In this work, we studied the effect of N-ethylmaleimide on permeability transition. The findings indicate that the amine inhibited the effects of carboxyatractyloside and agaric acid. It is known that...