Interesting facts
Interesting Facts about 3-Nitropropanoic Acid
3-Nitropropanoic acid is a fascinating organic compound with several noteworthy characteristics and applications. Here are some interesting facts about this compound:
- Structure and Reactivity: As a nitro compound, 3-nitropropanoic acid contains a nitro group (-NO2) that is attached to a propanoic acid backbone. This unique structure contributes to its reactivity and ability to participate in various chemical reactions.
- Biochemical Relevance: 3-Nitropropanoic acid is known as an inhibitor of the enzyme succinate dehydrogenase. This role is critical in metabolic studies, particularly in the context of mitochondrial function and energy production in cells.
- Toxicity: The compound is considered toxic to various organisms, highlighting its potential environmental and health impacts. Understanding its effects is essential for safety in handling and applications.
- Applications in Research: It is frequently utilized in biochemical research, particularly in studies related to metabolic diseases, neurobiology, and drug development. Researchers value its use as a tool to better understand complex biological systems.
- Analytical Methods: Various analytical techniques, such as chromatography and spectroscopy, are employed to study 3-nitropropanoic acid. These methods help scientists identify its presence and quantify its concentration in different samples.
In summary, 3-nitropropanoic acid serves as an important compound in both practical applications and scientific research, showcasing the intricate relationships between chemical structure, function, and biological activity.
Synonyms
3-nitropropionic acid
3-Nitropropanoic acid
504-88-1
Bovinocidin
Hiptagenic acid
beta-Nitropropionic acid
Propanoic acid, 3-nitro-
3-Nitropropionate
Propionic acid, 3-nitro-
beta-Nitropropanoic acid
3-NP acid
NCI-C03076
NSC 64266
NITROPROPIONIC ACID, BETA
.beta.-Nitropropionic acid
3-NPA
CCRIS 454
3-nitro-propionic acid
BOVINOCIDIN (3-nitropropionic acid)
Nitropropionic aci, beta
CHEBI:16348
HSDB 4147
QY4L0FOX0D
EINECS 208-003-0
MFCD00007406
beta-Nitropropanoate
BRN 1759889
DTXSID1020982
3-Nitroporpionic Acid
3-Nitro-Propanoic acid
NSC-64266
BNP
3-Nitropropionic acid, 8CI
DTXCID10982
CHEMBL451226
4-02-00-00771 (Beilstein Handbook Reference)
NSC64266
3-NITROPROPIONIC ACID [HSDB]
504-88-1 (FREE ACID)
3-nitro-1-propionate
3NP
3-NITROPROPIONICACID
CAS-504-88-1
SR-01000076030
UNII-QY4L0FOX0D
BNP; Bovinocidin; Hiptagenic Acid; NSC 64266; ss-Nitropropionic Acid
3Nitropropanoic acid
betaNitropropionic acid
Spectrum_001674
Propanoic acid, 3nitro
Propionic acid, 3nitro
SpecPlus_000692
beta -nitropropionic acid
Nitropropionic acid, 3-
Spectrum2_000876
Spectrum3_000993
Spectrum4_001119
Spectrum5_001895
Lopac-N-5636
WLN: WN2VQ
Nitropropionic acid, .beta.
Lopac0_000838
SCHEMBL70072
?-NITROPROPIONIC ACID
BSPBio_002685
KBioGR_001598
KBioSS_002154
MLS001066410
3-Nitropropionic acid, 97%
DivK1c_006788
SPECTRUM1504206
SPBio_000951
3-Nitropropionic acid, >=97%
BDBM82201
KBio1_001732
KBio2_002154
KBio2_004722
KBio2_007290
KBio3_001905
Propanoic acid, 3-nitro-(9CI)
HMS2235N03
HMS3262H17
HMS3369D16
HMS3865D03
Propanoic acid, 3-nitro- (9CI)
BCP15066
Tox21_202460
Tox21_303007
Tox21_500838
BDBM50480795
CCG-40325
s3652
AKOS006221915
AKOS015833440
CS-W013591
FN15632
HY-W012875
LP00838
SDCCGMLS-0066769.P001
SDCCGSBI-0050815.P003
NCGC00015744-01
NCGC00015744-02
NCGC00015744-03
NCGC00015744-04
NCGC00015744-05
NCGC00015744-06
NCGC00015744-07
NCGC00015744-11
NCGC00094169-01
NCGC00094169-02
NCGC00094169-03
NCGC00094169-04
NCGC00256389-01
NCGC00260009-01
NCGC00261523-01
SMR000471863
SY110140
3-Nitropropionic acid - CAS 504-88-1
DB-008848
EU-0100838
NS00032068
C05669
F17743
N 5636
Q223104
SR-01000076030-1
SR-01000076030-5
208-003-0
Solubility of 3-nitropropanoic acid
3-nitropropanoic acid (C3H5NO4) exhibits interesting solubility characteristics due to its molecular structure. Here are some key points regarding its solubility:
In summary, the solubility of 3-nitropropanoic acid is influenced by its polar functional groups, allowing it to dissolve effectively in polar solvents, particularly water and alcohols. As with many organic acids, understanding its solubility is crucial for applications in both synthetic and analytical chemistry.