|
METHYL ISOPROPYL KETONE | ||
PRODUCT IDENTIFICATION |
||
CAS NO. | 563-80-4 |
|
EINECS NO. | 209-264-3 | |
FORMULA | CH3C(O)CH(CH3)2 | |
MOL WT. | 86.13 | |
H.S. CODE | 2914.19.0000 | |
UN NO. |
2397 | |
TOXICITY |
Oral Rat LD50: 148mg/kg | |
SYNONYMS | Isopropyl methyl ketone; 3-Methyl-2-butanone; MIPK; | |
3-Methyl butan-2-one; 2-Acetyl propane; 2-Acetylpropane; 2-Methyl-3-butanone; Methyl butanone-2; Methyl isopropyl ketone; 3-Methylbutanone; Other RN: 52325-52-7 | ||
SMILES | C(C(C)=O)(C)C | |
CLASSIFICATION |
Ketone, Flavor and Fragrance agent |
|
EXTRA NOTES |
EPA Pesticide Chemical Code 044104. | |
PHYSICAL AND CHEMICAL PROPERTIES |
||
PHYSICAL STATE | colorless to pale yellow liquid | |
MELTING POINT | -92 C | |
BOILING POINT | 93 - 95 C | |
SPECIFIC GRAVITY |
0.80 - 0.81 | |
SOLUBILITY IN WATER | 6 (g/l) | |
SOLVENT SOLUBILITY | Soluble in Alcohol. Miscible with most common organic solvents | |
pH | ||
VAPOR DENSITY | ||
log P(o/w) | 0.84 (Octanol-water) | |
VAPOR PRESSURE | 52.2 (mmHg at 25 C) | |
HENRY LAW CONSTANT | 9.73E-05 (atm-m3/mole at 25 C) | |
OH RATE CONSTANT | 2.87E-12 (cm3/molecule-sec at 25 C Atmospheric ) | |
AUTOIGNITION |
475 C | |
NFPA RATINGS |
Health: 2 Flammability: 4 Reactivity: 0 | |
REFRACTIVE INDEX |
||
FLASH POINT |
-1 C | |
STABILITY | Stable under ordinary conditions. | |
EXTERNAL LINKS & GENERAL DESCRIPTION |
||
Wikipedia Linking (Butanone) Local: Carbonyl groups are:
Ketone has the general formula RCOR' where the groups R and R' may be the same or different, or incorporated into a ring (R and R' are alkyl, aryl, or heterocyclic radicals). The simplest example, R and R´ are methyl group, is acetone (also called 2-propanone, CH3COCH3) which is one of the most important ketones used in industry (low molecular weight ketones are general purpose solvents.) In the IUPAC system, the suffix -one is used to describe ketone with the numbering of the carbon atom at the end that gives the lower number. For example, CH3CH2COCH2CH2CH3 is named 3-hexanone because the whole chain contains six carbon atoms and the oxygen is connected to the third carbon from the lower number. There are aromatic ketones of which acetophenone and bezophenone are examples. Ketones can be made by the oxidation of secondary alcohols and the destructive distillation of certain salts of organic acids. In addition to as polar solvents, ketones are important intermediates in the syntheses of organic compounds such as alkoxides, hydroxyalkynes, imines, alcohols (primary, secondary as well as tertiary), acetals, thioacetals, phosphine oxides, geminal diols, hydrazones, organic sulfite and cyanohydrins. Methyl Isopropyl Ketone is used as a solvent and an intermediate in the synthesis of pharmaceuticals and pesticides. |
||
SALES SPECIFICATION | ||
APPEARANCE |
colorless to pale yellow liquid | |
PURITY |
99.0% min | |
MOISTURE | 0.5% max | |
TRANSPORTATION | ||
PACKING | 160kgs in drum | |
HAZARD CLASS | 3 (Packing group: II) | |
UN NO. | 2397 | |
SAFETY INFORMATION | ||
Hazard Symbols: F, Risk Phrases: 11, Safety Phrases: 9-16-33 | ||
PRICE INFORMATION | ||
|
|