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About This Item
Empirical Formula (Hill Notation):
C4H8O
CAS Number:
Molecular Weight:
72.11
UNSPSC Code:
12352005
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
102391
Assay:
≥99.0%
Grade:
SAJ first grade
Bp:
65-67 °C (lit.)
Vapor pressure:
114 mmHg ( 15 °C), 143 mmHg ( 20 °C)
Product Name
Tetrahydrofuran, SAJ first grade, ≥99.0%
grade
SAJ first grade
vapor density
2.5 (vs air)
vapor pressure
114 mmHg ( 15 °C), 143 mmHg ( 20 °C)
assay
≥99.0%
form
liquid
autoignition temp.
610 °F
contains
BHT as stabilizer
expl. lim.
1.8-11.8 %
availability
available only in Japan
dilution
(for analytical testing)
refractive index
n20/D 1.407 (lit.)
pH
~7
bp
65-67 °C (lit.)
mp
−108 °C (lit.)
density
0.889 g/mL at 25 °C (lit.)
SMILES string
C1CCOC1
InChI
1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI key
WYURNTSHIVDZCO-UHFFFAOYSA-N
Application
- Buffer systems for environmental toxicology: A study utilized buffer concentrates within a tiered regulatory framework for aquatic risk assessment of pesticides, emphasizing the critical role of standardized buffer systems in maintaining consistent experimental conditions (Santos et al., 2024).
- Buffer concentrate in pharmaceutical formulations: Buffer concentrates were used in the development of a prolonged permeation in situ gel for Levofloxacin HCl-Salicylic Acid, underlining the importance of buffer systems in drug release modulation and stability (Khaing et al., 2024).
- Buffer concentrate in diagnostic assays: The formulation of lateral flow devices for the detection of urinary biomarkers in kidney health assessments incorporated buffer concentrates to ensure optimal reagent performance and reaction kinetics (D Souza et al., 2024).
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signalword
Danger
supp_hazards
Storage Class
3 - Flammable liquids
flash_point_f
5.9 °F
flash_point_c
-14.5 °C
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system, Respiratory system
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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



