Skip to the beginning of the images gallery

2,2,3,3,3-Pentafluoro-1-propanol - 98%, high purity , CAS No.422-05-9

COA

Grade & Purity:

≥98%

Cas Number: 422-05-9
Molecular Weight: 150.05
Beilstein Registry Number: 1743133
EC Number: 207-012-7
MDL number: MFCD00004673
PubChem CID: 9872
PubChem SID: 488181042

In stock

Item Number

P122806

Grouped product items
SKU	Size	Availability	Price
P122806-5g	5g	5	$25.90
P122806-25g	25g	4	$97.90
P122806-100g	100g	2	$352.90

View related series

Non heterocyclic fluorine-containing block (1408) Oxygenated compounds (806)

Basic Description

Synonyms	J-506765 \| Pentafluoro-1-propanol \| NSC 66413 \| SCHEMBL20828 \| 1,1-Dihydroperfluoropropanol \| EN300-21115 \| FD2073 \| 1H,1H-perfluoropropanol \| PSQZJKGXDGNDFP-UHFFFAOYSA- \| SY018658 \| Q27277290 \| EPJ1S961SN \| 1H,1H-Pentafluoro-1-propanol \| AKOS000121412
Specifications & Purity	≥98%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	Generates fluorinated alpha-keto ethers with alkenes and has wide applications in the expanding fluorous research area Preparation of trifluoromethyl ynamines which, in turn, converted aldehydes to α-trifluoromethyl-α,β-uns?aturated amides. Application： 2,2,3,3,3-Pentafluoro-1-propanol has been used: as derivatization reagent in detection of unlabeled and 15N2 -labeled L-tryptophan, L-kynurenine, serotonin and quinolinic acid in human and rat plasma by GC-MS. as derivatization reagent in simultaneous analysis of cocaine, cocaethylene and their possible metabolic and pyrolytic products in blood, urine and muscle by GC-MS. preparation of trifluoromethyl ynamines which, in turn, converted aldehydes to α-trifluoromethyl-α,β-unsaturated amides. to generate fluorinated α-keto ethers with alkenes and has wide applications in the expanding fluorous research area.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organohalogen compounds
  - Class Halohydrins
    - Subclass Fluorohydrins

Kingdom	Organic compounds
Superclass	Organohalogen compounds
Class	Halohydrins
Subclass	Fluorohydrins
Intermediate Tree Nodes	Not available
Direct Parent	Fluorohydrins
Alternative Parents	Primary alcohols Organofluorides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Fluorohydrin - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organofluoride - Alkyl halide - Alkyl fluoride - Alcohol - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as fluorohydrins. These are alcohols substituted by a fluorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488181042
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488181042
IUPAC Name	2,2,3,3,3-pentafluoropropan-1-ol
INCHI	InChI=1S/C3H3F5O/c4-2(5,1-9)3(6,7)8/h9H,1H2
InChIKey	PSQZJKGXDGNDFP-UHFFFAOYSA-N
Smiles	C(C(C(F)(F)F)(F)F)O
Isomeric SMILES	C(C(C(F)(F)F)(F)F)O
WGK Germany	3
Molecular Weight	150.05
Beilstein	1743133
Reaxy-Rn	1743133
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1743133&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

16 results found

Lot Number	Certificate Type	Date	Item
G2510633	Certificate of Analysis	Jun 19, 2025	P122806
G2510634	Certificate of Analysis	Jun 19, 2025	P122806
G2510635	Certificate of Analysis	Jun 19, 2025	P122806
D2521263	Certificate of Analysis	Apr 09, 2025	P122806
D2521264	Certificate of Analysis	Apr 09, 2025	P122806
J2417712	Certificate of Analysis	Jun 22, 2024	P122806
J2417716	Certificate of Analysis	Jun 22, 2024	P122806
J2417732	Certificate of Analysis	Jun 22, 2024	P122806
A23311025	Certificate of Analysis	Jan 06, 2023	P122806
A23311242	Certificate of Analysis	Jan 06, 2023	P122806
A23311267	Certificate of Analysis	Jan 06, 2023	P122806
A23311266	Certificate of Analysis	Jan 06, 2023	P122806
A23311264	Certificate of Analysis	Jan 06, 2023	P122806
A23311024	Certificate of Analysis	Jan 06, 2023	P122806
B1419084	Certificate of Analysis	Feb 16, 2022	P122806
B1419083	Certificate of Analysis	Jan 25, 2022	P122806

Show more⌵

Chemical and Physical Properties

Sensitivity	Moisture sensitive
Refractive Index	1.288
Boil Point(°C)	80°C/748mmHg
Molecular Weight	150.050 g/mol
XLogP3	1.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	1
Exact Mass	150.01 Da
Monoisotopic Mass	150.01 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	94.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration