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2-METHYL-2-PROPAN(OL-D)

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2-METHYL-2-PROPAN(OL-D) Basic information

Product Name:
2-METHYL-2-PROPAN(OL-D)
Synonyms:
  • TERT-BUTAN-OL-D 98 PLUS ATOM % D
  • 2-METHYL-2-PROPAN(OL-D) 99 ATOM % D
  • tert-Butanol-OD >99.5 Atom % D
  • 2-Methyl-2-propan(ol-d), tert-Butanol-OD, tert-Butyl alcohol-d
  • TERT-BUTANOL-O-D, 98+ ATOM % D, FOR NMR
  • 1,1-Dimethyl(O-2H)ethanol
  • 2-[(2H)Hydroxy]-2-methylpropane
  • 2-Methyl-(O-2H)-2-propanol
CAS:
3972-25-6
MF:
C4H9DO
MW:
75.13
EINECS:
223-597-1
Mol File:
3972-25-6.mol
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2-METHYL-2-PROPAN(OL-D) Chemical Properties

Melting point:
23-26 °C (lit.)
Boiling point:
83 °C (lit.)
Density 
0.786 g/mL at 25 °C
refractive index 
n20/D 1.3847(lit.)
Flash point:
52 °F
storage temp. 
Flammables area
solubility 
Acetone, Chloroform (Slightly), Methanol (Slightly)
form 
Solid
color 
Colourless Oil to White
explosive limit
2.3-8.0%(V)
InChI
1S/C4H10O/c1-4(2,3)5/h5H,1-3H3/i5D
InChIKey
DKGAVHZHDRPRBM-UICOGKGYSA-N
SMILES
[2H]OC(C)(C)C
CAS Number Unlabeled
75-65-0
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Safety Information

Hazard Codes 
F,Xn
Risk Statements 
11-20-36/37
Safety Statements 
9-16-46
RIDADR 
UN 1120 3/PG 2
WGK Germany 
3
Storage Class
3 - Flammable liquids
Hazard Classifications
Acute Tox. 4 Inhalation
Eye Irrit. 2
Flam. Liq. 2
STOT SE 3

MSDS

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2-METHYL-2-PROPAN(OL-D) Usage And Synthesis

Chemical Properties

clear colorless liquid

Uses

Labelled Tert-butyl Alcohol is used as an organic solvent. Also it is used in the synthesis of proteosome inhibitors that are quite potent.

Uses

Tert-butyl Alcohol-OD is used as an organic solvent. Also it is used in the synthesis of proteosome inhibitors that are quite potent.

Synthesis

Deuterated tert-butanol can be used in organic synthesis, such as the preparation of ??,??-dideuterated alcohols, and an example of its application is as follows: in a 10 mL single-necked flask protected by nitrogen, 95.1 mg (0.50 mmol) of Compound 1d was added, 2.5 mL of tetrahydrofuran, 187.8 mg (2.50 mmol) of deuterated tert-butanol (t-BuOD), a 51.7 mg (2.25 mmol) sodium block, stirred for 5 min at 0 ??C. Raise to room temperature and burst the reaction with 3.0 M aqueous hydrochloric acid. Extracted by adding ether with saturated saline, the organic phase was dried, concentrated and separated by column chromatography to give 37.3 mg of the target compound in 54% yield.

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