HEXANOIC ANHYDRIDE
Synonym(s):Caproic anhydride
- CAS NO.:2051-49-2
- Empirical Formula: C12H22O3
- Molecular Weight: 214.3
- MDL number: MFCD00009509
- EINECS: 218-121-4
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-19 20:33:22
What is HEXANOIC ANHYDRIDE?
Chemical properties
clear colorless to light yellow liquid
The Uses of HEXANOIC ANHYDRIDE
Hexanoic anhydride has been used in:
- green synthesis of esters of acyclovir (acyclovir prodrugs)
- preparation of hexanoyl-modified chitosan nanoparticles and chitosan-based polymeric surfactants via N-acylation of chitosans
The Uses of HEXANOIC ANHYDRIDE
Hexanoic anhydride was used in:
- green synthesis of esters of acyclovir (acyclovir prodrugs)
- preparation of hexanoyl-modified chitosan nanoparticles
- preparation of chitosan-based polymeric surfactants via N-acylation of chitosans
The Uses of HEXANOIC ANHYDRIDE
Hexanoic Anhydride, is used as a reactant in the total synthesis of acremomannolipin A via steroselective β-mannosylation of 4,6,-O-benzylidene-protected mannosyl sulfoxide with a D-mannitol derivative.
What are the applications of Application
Hexanoic anhydride is a reactant in the synthesis of acremomannolipin A
Preparation
To an ice-cooled flask containing 116 gm (1.0 mole) of n-caproic acid is added 21.0-23.10 gm (0.5-0.55 mole) of ketene at a rate of 0.45 mole/hr. The reaction mixture is fractionally distilled at atmospheric pressure to afford a forecut of acetone, acetic acid, and acetic anhydride. The oil bath is raised to 220°C over a 1-hr period, kept there for 3 hr to ensure complete removal of acetic acid, and then cooled. The distillation is continued under reduced pressure to afford 86-95 gm (80-87%), b.p. 109- 112°C (3 mm Hg) and b.p. 118-121°C (6 mm Hg).
Flammability and Explosibility
Not classified
Properties of HEXANOIC ANHYDRIDE
Melting point: | -40 °C |
Boiling point: | 246-248 °C (lit.) |
Density | 0.928 g/mL at 20 °C (lit.) |
vapor pressure | 2.9Pa at 25℃ |
refractive index | n |
Flash point: | >230 °F |
storage temp. | Store below +30°C. |
solubility | ethanol: soluble1g/10 mL, clear, colorless |
form | Liquid |
color | Clear colorless to light yellow |
explosive limit | 0.7%(V) |
Water Solubility | Hydrolyzes in water. |
Sensitive | Moisture Sensitive |
BRN | 1776561 |
CAS DataBase Reference | 2051-49-2(CAS DataBase Reference) |
EPA Substance Registry System | Hexanoic acid, anhydride (2051-49-2) |
Safety information for HEXANOIC ANHYDRIDE
Signal word | Danger |
Pictogram(s) |
Corrosion Corrosives GHS05 |
GHS Hazard Statements |
H314:Skin corrosion/irritation |
Precautionary Statement Codes |
P280:Wear protective gloves/protective clothing/eye protection/face protection. P363:Wash contaminated clothing before reuse. P303+P361+P353:IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P405:Store locked up. |
Computed Descriptors for HEXANOIC ANHYDRIDE
Abamectin manufacturer
JPN Pharma Pvt Ltd
Proto Chemicals Industries
Ishant Polychem
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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