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CAS No.: | 76-09-5 |
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Name: | Pinacol |
Molecular Structure: | |
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Formula: | C6H14O2 |
Molecular Weight: | 118.176 |
Synonyms: | 1,1,2,2-Tetramethylethyleneglycol;2,3-Dihydroxy-2,3-dimethylbutane;2,3-Dimethyl-2,3-butanediol;2,3-Dimethyl-2,3-dihydroxybutane;NSC 25943;Pinacone;Tetramethylethylene glycol;2,3-Dimethyl-butane-2,3-diol;2,3-Butanediol,2,3-dimethyl-; |
EINECS: | 200-933-5 |
Density: | 0.963 g/cm 3 |
Melting Point: | 40-43 °C(lit.) |
Boiling Point: | 174.4 °C at 760 mmHg |
Flash Point: | 77.2 °C |
Solubility: | Soluble in hot water, alcohol, and diethyl ether. |
Appearance: | white solid |
Hazard Symbols: |
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Risk Codes: | 38-36/37/38 |
Safety: | 37-37/39-26 |
Transport Information: | UN 1325 4.1/PG 2 |
PSA: | 40.46000 |
LogP: | 0.52820 |
2,3-dimethyl-2,3-epoxybutane
A
3,3-dimethyl-butan-2-one
B
2,3-dimethyl-2,3-butane diol
C
2,3-dimethyl-1-buten-3-ol
Conditions | Yield |
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With perchloric acid; sodium perchlorate at 25℃; Yields of byproduct given; | A n/a B 99.93% C n/a |
With perchloric acid; sodium perchlorate at 25℃; Product distribution; heterogeneous reaction; |
Conditions | Yield |
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With methanol; gallium nitride at 20℃; for 12h; Irradiation; Sealed tube; | 99% |
With potassium bromate; hydrogenchloride; mercury(II) diacetate at 35℃; for 0.666667h; Equilibrium constant; | |
durch elektrolytische Reduktion; |
Conditions | Yield |
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In ethanol for 0.166667h; Heating; Yields of byproduct given; | A n/a B 99% |
Conditions | Yield |
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In ethanol for 0.25h; Heating; Yields of byproduct given; | A n/a B 99% |
mercury(II) trifluoroacetate
A
2,3-dimethyl-2,3-butane diol
Conditions | Yield |
---|---|
In ethanol for 0.25h; Heating; Yields of byproduct given; | A n/a B 99% |
Conditions | Yield |
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With K2; (DHQD)2 quinuclidine; potassium hexacyanoferrate(III) In water; tert-butyl alcohol at 25℃; for 5h; pH=12; Oxidation; | 98% |
With 1,4-diaza-bicyclo[2.2.2]octane; K2; oxygen In water; tert-butyl alcohol at 50℃; under 750.075 Torr; for 18h; pH=12.0; | 94% |
With Nafion NR50; dihydrogen peroxide at 70℃; for 20h; | 86% |
Conditions | Yield |
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In ethanol for 0.166667h; Heating; Yields of byproduct given; | A n/a B 97% |
4,4,5,5-tetramethyl-1,3-dioxolan-2-one
A
methanol
B
2,3-dimethyl-2,3-butane diol
Conditions | Yield |
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With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium tert-butylate; hydrogen In tetrahydrofuran at 140℃; for 20h; Autoclave; | A 95 %Chromat. B 96% |
With (bis[(2-diisopropylphosphino)ethyl]amine)Mn(CO)2Br; hydrogen; sodium t-butanolate In tetrahydrofuran at 120℃; under 22502.3 Torr; for 26h; Schlenk technique; Glovebox; Autoclave; | A 66% B 76% |
With potassium phosphate; C62H63N5OPRu(1+)*Cl(1-); hydrogen In tetrahydrofuran at 140℃; under 38002.6 Torr; for 24h; Glovebox; Autoclave; | A 93 %Chromat. B 99 %Chromat. |
Conditions | Yield |
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In ethanol for 0.25h; Heating; Yields of byproduct given; | A n/a B 95% |
Conditions | Yield |
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With C34H32N4O2RuSe4 In 1,1,1,3',3',3'-hexafluoro-propanol at 23℃; for 4h; Inert atmosphere; | A 94% B n/a |
1. Introduction of Pinacol
Pinacol is a white solid organic compound. It is an alcohol that has -OH groups on adjacent carbon atoms on the same side.
2. Properties of Pinacol
The density of Pinacol(76-09-5) is 0.963 g/cm3 and it has a melting point of 40-43 °C(lit.). The boiling point is 174.4 °C at 760 mmHg. The refractive index is about 1.448. Its flash point is 77.2 °C.
3. Toxicity of Pinacol
LD50/LC50: RTECS:
CAS# 76-09-5: Draize test, rabbit, skin: 500 mg/24H Moderate;
Oral, mouse: LD50 = 3380 mg/kg;
Carcinogenicity: Pinacol - Not listed as a carcinogen by ACGIH, IARC, NTP, or CA Prop 65.
Other: The toxicological properties have not been fully investigated. See actual entry in RTECS for complete information.
4. Safety Information of Pinacol
Hazard Codes:Xi
Risk Statements:
R38:Irritating to skin.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements:
S37:Wear suitable gloves.
S37/39:Wear suitable gloves and eye/face protection.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
RIDADR UN: 1325 4.1/PG 2
WGK Germany: 2
RTECS EK:1720000
F: 3
5. Preparation of Pinacol
Pinacol may be produced by the pinacol coupling reaction from acetone.
6. Use of Pinacol
Pinacol can be use with borane and boron trichloride to produce useful synthetic intermediate such as pinacolborane, bis(pinacolato)diboron, and pinacolchloroborane