4-Fluorobutanol

4-Fluorobutanol
Names
	Preferred IUPAC name 4-Fluorobutan-1-ol
Identifiers
CAS Number	372-93-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	9372;
PubChem CID	9755;
	InChI InChI=1S/C4H9FO/c5-3-1-2-4-6/h6H,1-4H2 Key: SHOBGSRUFRALBO-UHFFFAOYSA-N;
	SMILES C(CCF)CO;
Properties
Chemical formula	C4H9FO
Molar mass	92.113 g·mol−1
Boiling point	129.3 °C (264.7 °F; 402.4 K)
Solubility in water	miscible
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H226, H315, H319, H335
GHS precautionary statements	P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405, P501
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	0.9 mg·kg−1(mouse, injected IP or SC)
Related compounds
Related compounds	1,4-dichlorobutane; 1,4-butanediol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

4-Fluorobutanol is a chemical compound, a flammable colorless liquid which is a fluorinated alcohol. Like 2-fluoroethanol, it is highly toxic due to its ready metabolism to fluoroacetate.^[1]^[2]

References

↑ "Toxic Fluorine Compounds". Nature 172 (4390): 1139–1141. 1953. doi:10.1038/1721139a0. PMID 13111268. Bibcode: 1953Natur.172.1139P.
↑ Pattison, F. L. M.; Howell, W. C.; McNamara, A. J.; Schneider, J. C.; Walker, J. F. (1956). "Toxic Fluorine Compounds. III.¹ ω-Fluoroalcohols.". The Journal of Organic Chemistry 21 (7): 739–747. doi:10.1021/jo01113a006.

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[1] "Toxic Fluorine Compounds". Nature 172 (4390): 1139–1141. 1953. doi:10.1038/1721139a0. PMID 13111268. Bibcode: 1953Natur.172.1139P.

[2] Pattison, F. L. M.; Howell, W. C.; McNamara, A. J.; Schneider, J. C.; Walker, J. F. (1956). "Toxic Fluorine Compounds. III.¹ ω-Fluoroalcohols.". The Journal of Organic Chemistry 21 (7): 739–747. doi:10.1021/jo01113a006.

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[2]

4-Fluorobutanol

Topic: Chemistry

See also

References