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Merck
CN

33067

tert-Butanol

puriss. p.a., ACS reagent, reag. Ph. Eur., ≥99.5% (GC)

Synonym(s):

2-Methyl-2-propanol, tert-Butyl alcohol, Trimethyl carbinol

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About This Item

Linear Formula:
(CH3)3COH
CAS Number:
Molecular Weight:
74.12
EC Number:
200-889-7
UNSPSC Code:
12190000
PubChem Substance ID:
Beilstein/REAXYS Number:
906698
MDL number:
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agency

reag. Ph. Eur.

vapor density

2.5 (vs air)

vapor pressure

31 mmHg ( 20 °C), 44 mmHg ( 26 °C)

grade

ACS reagent, puriss. p.a.

assay

≥99.5% (GC)

autoignition temp.

896 °F

expl. lim.

8 %

impurities

≤0.001% free acid (as C3H7COOH), ≤0.001% non-volatile matter, ≤0.01% carbonyl compounds (as HCHO), ≤0.1% water (Karl Fischer), ≤0.5% 2-butanol

refractive index

n25/D 1.3845-1.3855, n20/D 1.387 (lit.)

bp

83 °C (lit.)

mp

23-26 °C (lit.)

transition temp

solidification point 25-26 °C

density

0.775 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg, B: ≤0.02 mg/kg, Ba: ≤0.1 mg/kg, Ca: ≤0.5 mg/kg, Cd: ≤0.05 mg/kg, Co: ≤0.02 mg/kg, Cr: ≤0.02 mg/kg, Cu: ≤0.02 mg/kg, Fe: ≤0.1 mg/kg, Mg: ≤0.1 mg/kg, Mn: ≤0.02 mg/kg, Ni: ≤0.02 mg/kg, Pb: ≤0.1 mg/kg, Sn: ≤0.1 mg/kg, Zn: ≤0.1 mg/kg

SMILES string

CC(C)(C)O

InChI

1S/C4H10O/c1-4(2,3)5/h5H,1-3H3

InChI key

DKGAVHZHDRPRBM-UHFFFAOYSA-N



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pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system, Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

59.0 °F - closed cup

flash_point_c

15 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Tesfamichael H Kebrom et al.
Plant, cell & environment, 38(8), 1471-1478 (2014-12-17)
Shoot branches or tillers develop from axillary buds. The dormancy versus outgrowth fates of buds depends on genetic, environmental and hormonal signals. Defoliation inhibits bud outgrowth indicating the role of leaf-derived metabolic factors such as sucrose in bud outgrowth. In
Jaime Salazar et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 81(1), 82-90 (2012-01-12)
Nanosizing is a non-specific approach to improve the oral bioavailability of poorly soluble drugs. The decreased particle size of these compounds results in an increase in surface area. The outcome is an increased rate of dissolution, which can lead to
Arnau Bassegoda et al.
Applied microbiology and biotechnology, 97(19), 8559-8568 (2013-01-22)
Rhodococci are highly adaptable bacteria, capable to degrade or transform a large number of organic compounds, including recalcitrant or toxic products. However, little information is available on the lipases of the genus Rhodococcus, except for LipR, the first lipase isolated