citric acid
Megjelenés
|
| |||
| Names | |||
|---|---|---|---|
| IUPAC name
Citric acid[1] | |||
| Preferred IUPAC name
2-Hydroxypropane-1,2,3-tricarboxylic acid[1] | |||
| Identifiers | |||
3D model (JSmol) |
|||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| DrugBank | |||
| EC Number |
| ||
| KEGG | |||
PubChem CID |
|||
| RTECS number |
| ||
| UNII | |||
| |||
| |||
| Properties | |||
| C6H8O7 | |||
| Molar mass | 192.123 g/mol (anhydrous), 210.14 g/mol (monohydrate)[2] | ||
| Appearance | white solid | ||
| Odor | Odorless | ||
| Density | 1.665 g/cm3 (anhydrous) 1.542 g/cm3 (18 °C, monohydrate) | ||
| Melting point | 156 °C (313 °F; 429 K) | ||
| Boiling point | 310 °C (590 °F; 583 K) decomposes from 175 °C[3] | ||
| 54% w/w (10 °C) 59.2% w/w (20 °C) 64.3% w/w (30 °C) 68.6% w/w (40 °C) 70.9% w/w (50 °C) 73.5% w/w (60 °C) 76.2% w/w (70 °C) 78.8% w/w (80 °C) 81.4% w/w (90 °C) 84% w/w (100 °C)[4] | |||
| Solubility | Soluble in acetone, alcohol, ether, ethyl acetate, DMSO Insoluble in benzene, CHCl3, CS2, toluene[3] | ||
| Solubility in ethanol | 62 g/100 g (25 °C)[3] | ||
| Solubility in amyl acetate | 4.41 g/100 g (25 °C)[3] | ||
| Solubility in diethyl ether | 1.05 g/100 g (25 °C)[3] | ||
| Solubility in 1,4-dioxane | 35.9 g/100 g (25 °C)[3] | ||
| log P | −1.64 | ||
| Acidity (pKa) | pKa1 = 3.13[5] pKa2 = 4.76[5] pKa3 = 6.39,[6] 6.40[7] pKa4 = 14.4[8] | ||
Refractive index (nD) |
1.493–1.509 (20 °C)[4] 1.46 (150 °C)[3] | ||
| Viscosity | 6.5 cP (50% aq. sol.)[4] | ||
| Structure | |||
| Monoclinic | |||
| Thermochemistry | |||
| 226.51 J/(mol·K) (26.85 °C)[9] | |||
| 252.1 J/(mol·K)[9] | |||
| −1543.8 kJ/mol[4] | |||
| 1985.3 kJ/mol (474.5 kcal/mol, 2.47 kcal/g),[4] 1960.6 kJ/mol[9] 1972.34 kJ/mol (471.4 kcal/mol, 2.24 kcal/g) (monohydrate)[4] | |||
| Pharmacology | |||
| A09AB04 (WHO) | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Skin and eye irritant | ||
| GHS labelling: | |||
| Warning | |||
| H290, H319, H315[5] | |||
| P305+P351+P338[5] | |||
| NFPA 704 (fire diamond) | |||
| Flash point | 155 °C (311 °F; 428 K) | ||
| 345 °C (653 °F; 618 K) | |||
| Explosive limits | 8%[5] | ||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
3000 mg/kg (rats, oral) | ||
| Safety data sheet (SDS) | HMDB (PDF) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |||
Főnév
citric acid (tsz. citric acids)
- citric acid - Szótár.net (en-hu)
- citric acid - Sztaki (en-hu)
- citric acid - Merriam–Webster
- citric acid - Cambridge
- citric acid - WordNet
- citric acid - Яндекс (en-ru)
- citric acid - Google (en-hu)
- citric acid - Wikidata
- citric acid - Wikipédia (angol)
- 1 2
- ↑ Sablon:PubChemLink
- 1 2 3 4 5 6 7 citric acid. chemister.ru. [2014. november 29-i dátummal az eredetiből archiválva].
- 1 2 3 4 5 6 Sablon:PubChemLink
- 1 2 3 4 5 6 Fisher Scientific, Citric acid. Retrieved on 2014-06-02.
- ↑ Data for Biochemical Research. ZirChrom Separations, Inc
- ↑ Ionization Constants of Organic Acids. Michigan State University
- ↑
- 1 2 3 Sablon:nist
Kategóriák:
- Chemical articles with multiple compound IDs
- Multiple chemicals in an infobox that need indexing
- Chemical articles with multiple PubChem CIDs
- Chembox having GHS data
- Articles containing unverified chemical infoboxes
- Chembox image size set
- angol-magyar szótár
- angol lemmák
- angol főnevek
- angol megszámlálható főnevek
- angol kifejezések
- en:Gyógyszertan



