ChemicalBook--->CAS DataBase List--->338-83-0

338-83-0

338-83-0 Structure

338-83-0 Structure
IdentificationMore
[Name]

Perfluorotripropylamine
[CAS]

338-83-0
[Synonyms]

1,1,2,2,3,3,3-heptafluoro-n,n-bis(heptafluoropropyl)-1-propanamine
PERFLUOROTRIPROPYLAMINE
1,1,2,2,3,3,3-heptafluoro-n,n-bis(heptafluoropropyl)-1-propanamin
Heneicosafluorotripropylamine
Heptafluoro-N,N-bis(heptafluoropropyl)-1-propanamine
Perfluamine
Tris(heptafluoropropyl)amine
tris-(heptafluoropropyl)-amine
Tris(heptafluoro-propyl)amine
tris-heptafluoropropyl-amine
Perfluoro-tri-n-propylamine
Perfluorotripropylamine 90%
Perfluorotripropylamine90%
FC-3283
FTPA
Perfluoropropylamine
Tri(heptafluoropropyl)amine
Tris(perfluoropropyl)amine
[EINECS(EC#)]

206-420-2
[Molecular Formula]

C9F21N
[MDL Number]

MFCD00042589
[Molecular Weight]

521.07
[MOL File]

338-83-0.mol
Chemical PropertiesBack Directory
[Melting point ]

-52 °C
[Boiling point ]

125-135°C
[density ]

1.82
[vapor pressure ]

5.16hPa at 20℃
[refractive index ]

1.279
[storage temp. ]

-20°C, Inert atmosphere
[solubility ]

DMSO (Slightly), Methanol (Slightly), Water (Slightly)
[form ]

Oil
[pka]

-27.02±0.50(Predicted)
[color ]

Colourless
[InChI]

InChI=1S/C9F21N/c10-1(11,4(16,17)18)7(25,26)31(8(27,28)2(12,13)5(19,20)21)9(29,30)3(14,15)6(22,23)24
[InChIKey]

JAJLKEVKNDUJBG-UHFFFAOYSA-N
[SMILES]

C(F)(F)(N(C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)F
[LogP]

5.3-6.1
[CAS DataBase Reference]

338-83-0(CAS DataBase Reference)
[NIST Chemistry Reference]

1-Propanamine, 1,1,2,2,3,3,3-heptafluoro-N,N-bis(heptafluoropropyl)-(338-83-0)
[EPA Substance Registry System]

338-83-0(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H300-H317-H402
[Precautionary statements ]

P501-P261-P273-P272-P270-P264-P280-P302+P352-P362+P364-P333+P313-P301+P310+P330-P405
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

UN2735
[WGK Germany ]

WGK 3
[Hazard Note ]

Irritant
[TSCA ]

T
[REACH Registrations]

Active
[HazardClass ]

8
[HS Code ]

2921199990
[Storage Class]

10 - Combustible liquids
[Hazardous Substances Data]

338-83-0(Hazardous Substances Data)
Hazard InformationBack Directory
[Uses]

Perfluorotripropylamine (338-83-0) is a reagent used in the surface modification of droplet polymeric microfluidic devices. This is used to improve the stable and continueous generation of aqueous droplets.
[Application]

The half-life of perfluorotripropylamine (338-83-0) is 65 days, with excellent emulsification properties[1]. This perfluorocarbon chemical is also used in the following field:
Used as corrosion inhibitor, transmission fluid, and dielectric insulating oil for instruments.
Used as leakage detection liquid of electronic components and devices.
Used as antioxidant lubricant
Used as a cleaning agent for electronics, CD-ROM, and precision instruments.
[Definition]

ChEBI: Perfluorotripropylamine is an organofluorine compound. It has a role as a blood substitute. It is functionally related to a tripropylamine.
[Clinical Use]

Perfluorotripropylamine (PFTA, FTPA or FC-3283, 338-83-0), with the chemical formula N(CF?–CF?–CF?)?, is a fluorinated amine compound. In the medical field, it is used as a plasma volume expander, i.e. an oxygen-carrying agent (blood substitute) used as a red blood cell substitute [2]. In a medical model, it was encapsulated within a copolymer as a perfluorocarbon oxygen carrier; a PLGA-PEG/FC-3283 emulsion was prepared using poly(lactic-co-glycolic acid) (PLGA) modified with polyethylene glycol (PEG) for the purpose of highly efficient cellular reoxygenation. HCT 116 cells subjected to hypoxia treatment showed a significant increase in viability following treatment with this emulsion [3].
[Purification Methods]

Purify it as for perfluorodimethyl-cyclopropane (see p 220). [Haszeldine J Chem Soc 102 1951, for azeotropes see Simons & Linevsky J Am Chem Soc 74 4750 1972.] IRRITANT.
[References]

[1] Cohn, S M. “Blood substitutes in surgery.” Surgery 127 6 (2000): 599–602.
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