Grundinformationen
- CAS
565-70-8- Standard-SMILES
CCC(O)C(=O)O- InChIKey
AFENDNXGAFYKQO-UHFFFAOYSA-N- Summenformel
- C4H8O3
- Durchschnittliche Molmasse
- 104,1 g/mol
- Monoisotopische Masse
- 104,04734411
Namen und Bezeichner
- Bevorzugter Name
- 2-Hydroxybutyric Acid
- IUPAC
- 2-hydroxybutanoic acid
- Lokaler Name
- (±)-2-Hydroxybuttersure
- Englischer Name
- DL-2-Hydroxybutyric Acid
- Summenformel
- C4H8O3
- Molmasse
- 104.1
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
565-70-8、600-15-7- PubChem CID
- 11266
- DTXSID
DTXSID8041903- ChEMBL
CHEMBL567588- ChEBI
CHEBI:1148- UNII
- O0ADR0I4H5
- EC Number
- 209-985-3
- Nikkaji
- J130.629D、J2.433.029J
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,1
- Polarare Oberfläche (TPSA)
- 57,5 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 7
- Formalladung
- 0
- Komplexität
- 69
Experimentelle und physikochemische Eigenschaften
Collision Cross Section
124.67 Ų [M-H]- [CCS Type: DT; Method: stepped-field]
120.5 Ų [M-H]-
Physikochemische Eigenschaften
- Schmelzpunkt
- 44 °C · 44 °C
- Siedepunkt
- 260 °C · 260 °C
- Dichte
- 1.125 · 1.1250
- Brechungsindex
- 1.4298 · 1.4298 (589.3 nm 20℃)
- storage temp.
- Refrigerator
- Löslichkeit
- Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
- Aggregatzustand
- Solid
- pka
- 1 · pK1:3.65 (30°C)
- Farbe
- White to Off-White
- Merck
- 14 · 14,4816
- InChI
- InChI=1S/C4H8O3/c1-2-3(5)4(6)7/h3,5H,2H2,1H3,(H,6,7)
- InChIKey
- AFENDNXGAFYKQO-UHFFFAOYSA-N
- SMILES
- C(O)(=O)C(O)CC
- EPA chemische Informationen
- 2 · Butanoic acid, 2-hydroxy- (600-15-7)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation];H318 (25%): Causes serious eye damage [Danger Serious eye damage/eye irritation];H319 (75%): Causes serious eye irritation [Warning Serious eye damage/eye irritation];H335 (75%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 4 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- WGK 3
- hs_code
- 2918199890
- risk_code
- 36/37/38-41-37/38
- hazard_code
- Xi
- safety_code
- 26-36/37/39-39
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Dam. 1Skin Irrit. 2STOT SE 3
Chemie und Industrie
Anwendungen
Beschreibung2-Hydroxybutyric acid (or alpha - hydroxy butyrate) is a hydroxy butyric acid with the hydroxyl group on the carbon adjacent to the carboxyl. It is a chiral compound having two enantiomers, D-2- hydroxybutyric acid and L-2-hydroxybutyric acid. 2-Hydroxy butyrate, the conjugate base of 2-hydroxy butyric acid, is produced in mammalian tissues (principally hepatic) that catabolize L-threonine or synthesize glutathione. Oxidative stress or detoxification demands can dramatically increase the rate of hepatic glutathione synthesis. Under such metabolic stress conditions, supplies of L-cysteine for glutathione synthesis become limiting, so homocysteine is diverted from the transmethylation pathway forming methionine into the transsulfuration pathway forming cystathionine. 2-Hydroxybutyrate is released as a byproduct when cystathionine is cleaved to cysteine that is incorporated into glutathione. Chronic shifts in the rate of glutathione synthesis may be reflected by urinary excretion of 2-hydroxybutyrate.
Verwenden2-Hydroxybutanoic Acid is an analyte used in the diagnoses of colorectal cancer as well as Type II diabetes. It is also used in the purification of the major Vibrio autoinducer and the study of its role in virulence factor production for cholera.
Anbieter6 Anbieter
Ergänzende Hinweise
DefinitionChEBI: A hydroxybutyric acid having a single hydroxyl group located at position 2; urinary secretion of 2-hydroxybutyric acid is increased with alcohol ingestion or vigorous physical exercise and is associated with lactic acidosis and ketoacidosis in humans and d abetes in animals.
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