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270385

Tetrahydrofuran

≥99.9%, HPLC grade, suitable for HPLC, inhibitor-free

Synonym(s):

THF, Butylene oxide, Oxolane, Tetramethylene oxide

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About This Item

Empirical Formula (Hill Notation):
C4H8O
CAS Number:
109-99-9
Molecular Weight:
72.11
UNSPSC Code:
12190000
PubChem Substance ID:
329752934
EC Number:
203-726-8
Beilstein/REAXYS Number:
102391
MDL number:
MFCD00005356
Assay:
≥99.9%
Grade:
HPLC grade
Technique(s):
HPLC: suitable
Bp:
65-67 °C
Vapor pressure:
114 mmHg ( 15 °C), 143 mmHg ( 20 °C)
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Product Name

Tetrahydrofuran, HPLC grade, ≥99.9%, inhibitor-free

grade

HPLC grade

vapor density

2.5 (vs air)

vapor pressure

114 mmHg ( 15 °C), 143 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

610 °F

purified by

glass distillation

expl. lim.

1.8-11.8 %

technique(s)

HPLC: suitable

impurities

<0.020% water

evapn. residue

<0.0005%

refractive index

n20/D 1.407 (lit.)

bp

65-67 °C

mp

−108 °C (lit.)

density

0.889 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 212 nm Amax: 1.00, λ: 250 nm Amax: 0.18, λ: 300 nm Amax: 0.02, λ: 350-400 nm Amax: 0.01

SMILES string

C1CCOC1

InChI

1S/C4H8O/c1-2-4-5-3-1/h1-4H2

InChI key

WYURNTSHIVDZCO-UHFFFAOYSA-N

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signalword

Danger

target_organs

Central nervous system, Respiratory system

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

flash_point_f

-6.2 °F - closed cup

flash_point_c

-21.2 °C - closed cup

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3

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Certificates of Analysis (COA)

Lot/Batch Number
05310CW
02412AW
10503DW
09926BX
07815CX

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Tetrahydrofuran-containing macrolides: a fascinating gift from the deep sea.
Adriana Lorente et al.
Chemical reviews, 113(7), 4567-4610 (2013-03-20)
Ryan D Pensack et al.
Journal of the American Chemical Society, 137(21), 6790-6803 (2015-05-07)
We compare the singlet fission dynamics of five pentacene derivatives precipitated to form nanoparticles. Two nanoparticle types were distinguished by differences in their solid-state order and kinetics of triplet formation. Nanoparticles that comprise primarily weakly coupled chromophores lack the bulk
P T Clayton et al.
The Journal of clinical investigation, 79(4), 1031-1038 (1987-04-01)
Urinary bile acids from a 3-mo-old boy with cholestatic jaundice were analyzed by ion exchange chromatography and gas chromatography-mass spectrometry (GC-MS). This suggested the presence of labile sulfated cholenoic acids with an allylic hydroxyl group, a conclusion supported by analysis
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