Trifluoromethanesulfonic acid supplier

Name
Trifluoromethanesulfonic acid
EINECS 216-087-5
CAS No. 1493-13-6
Article Data90
CAS DataBase
Density 1.877 g/cm³
Solubility soluble in water
Melting Point -40 °C
Formula CHF₃O₃S
Boiling Point 161.999 °C at 760 mmHg
Molecular Weight 150.078
Flash Point None
Transport Information UN 3265 8/PG 2
Appearance Colourless liquid with a pungent odour
Safety 26-36/37/39-45
Risk Codes 21/22-35-10
Molecular Structure
Hazard Symbols C
Synonyms Trifluoromethane sulfonic acid;Methanesulfonicacid, trifluoro- (6CI,7CI,8CI,9CI);Fluorad FC 24;Perfluoromethanesulfonicacid;Triflic acid;Trimsylate;
PSA 62.75000
LogP 1.47480

Synthetic route

: [η5-C5Me5Ru(μ-SiPr)2Ru(OH2)-η5-C5Me5](OTf)2

: 1333-74-0
hydrogen

A: 1493-13-6
trifluorormethanesulfonic acid

B: C26H45Ru2S2(1+)*CF3O3S(1-)

Conditions

Conditions	Yield
In dichloromethane; water at 20℃; for 1h; Schlenk technique; Inert atmosphere;	A n/a B 98%

...Expand

: 335-05-7
Trifluoromethanesulfonyl fluoride

: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
With sulfuric acid Reagent/catalyst;	97.5%
at 100°C for 48 h;	50%
at 20°C for 48 h;	7%

: 2926-30-9
sodium triflate

: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
With sulfuric acid	97.1%

: 33454-82-9
lithium trifluoromethanesulfonate

: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
With sulfuric acid	96.8%

: ferrocenium trifluoromethanesulfonate

A: 102-54-5
ferrocene

B: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
With C26H46ClO3Ru2S2(1+)*CF3O3S(1-); hydrogen In water at 20℃; under 760.051 Torr; for 1.2h; Catalytic behavior; Temperature; Reagent/catalyst; Inert atmosphere; Schlenk technique;	A 95% B n/a
With [(pentamethylcyclopentadienyl)Ru{PhP(C6H4-o-S)2}Ru(pentamethylcyclopentadienyl)](OTf)2; hydrogen In water at 20℃; under 760.051 Torr; for 20h;	A 87% B 86%
With [η5-C5Me5Ru(μ-SiPr)2Ru(OH2)-η5-C5Me5](OTf)2; hydrogen In methanol at 20℃; under 760.051 Torr; for 1.4h; Temperature; Reagent/catalyst; Solvent; Pressure; Schlenk technique;

: 67-66-3
chloroform

: 65597-24-2
Chlorine(I) trifluoromethanesulfonate

A: 1493-13-6
trifluorormethanesulfonic acid

B: 358-23-6
trifluoromethylsulfonic anhydride

Conditions

Conditions	Yield
at 22℃; for 1h;	A n/a B 92%

...Expand

: 82582-46-5
(η5-C5H5)Re(NO)(PPh3)(COCH3)

: 358-23-6
trifluoromethylsulfonic anhydride

: 865-47-4
potassium tert-butylate

A: 82582-34-1
{(η5-C5H5)Re(NO)(PPh3)(vinylidene)}(CF3SO3)

B: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
In dichloromethane	A 88% B n/a

...Expand

: 768-66-1
2,2,6,6-tetramethyl-piperidine

: 82582-46-5
(η5-C5H5)Re(NO)(PPh3)(COCH3)

: 358-23-6
trifluoromethylsulfonic anhydride

A: 82582-34-1
{(η5-C5H5)Re(NO)(PPh3)(vinylidene)}(CF3SO3)

B: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
In dichloromethane (CF3SO2)2O added to a stirred soln. of CpRe(NO)(PPh3)(COCH3) in CH2Cl2 at -78°C, after 10 min addn. of TMP, stirring for 1 h at -78°C, (CF3SO2)2O added, after 10 min soln. warmed to room temp., filtration, solvent removed by rotary evapn.;; extn. (CHCl3), extract filtered, solvent removed by rotary evapn.; monitored by (1)H- and (31)P-NMR-spectroscopy (-80°C, CD2Cl2 or CH2Cl2, < 5 min);;	A 88% B n/a

Yield

In dichloromethane (CF3SO2)2O added to a stirred soln. of CpRe(NO)(PPh3)(COCH3) in CH2Cl2 at -78°C, after 10 min addn. of TMP, stirring for 1 h at -78°C, (CF3SO2)2O added, after 10 min soln. warmed to room temp., filtration, solvent removed by rotary evapn.;; extn. (CHCl3), extract filtered, solvent removed by rotary evapn.; monitored by (1)H- and (31)P-NMR-spectroscopy (-80°C, CD2Cl2 or CH2Cl2, < 5 min);;

A 88%
B n/a

...Expand

: (E)-1-(4-chlorophenyl)-N-(4-methoxyphenyl)methanimine

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-3-phenoxyazetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 75%

...Expand

: 110-91-8
morpholine

: 71001-09-7
1,2:3,4-di-O-isopropylidene-6-O-trifluoromethanesulfonyl-α-D-galactopyranose

A: 1493-13-6
trifluorormethanesulfonic acid

B: 98979-39-6
1,2:3,4-di-O-isopropylidene-6-morpholino-α-D-galactopyranose

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 24h; Ambient temperature;	A n/a B 74%

...Expand

: 626-58-4
4-methylpiperidin

: 71001-09-7
1,2:3,4-di-O-isopropylidene-6-O-trifluoromethanesulfonyl-α-D-galactopyranose

A: 1493-13-6
trifluorormethanesulfonic acid

B: 1,2:3,4-di-O-isopropylidene-6-(4-methylpiperidino)-α-D-galactopyranose

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 24h; Ambient temperature;	A n/a B 67%

...Expand

: 768-66-1
2,2,6,6-tetramethyl-piperidine

: 115365-02-1
(η5-C5H5)Re(NO)(PPh3)(COCH2(1-C10H7))

: 358-23-6
trifluoromethylsulfonic anhydride

: 115365-04-3
sc-{(η5-C5H5)Re(NO)(PPh3)(CCH(1-C10H7))}(CF3SO3)

B: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
In dichloromethane react. monitored by (1)H- and (31)P-NMR-spectroscopy (-80°C, CD2Cl2 or CH2Cl2, < 5 min); elem. anal.; sc/ac-ratio>99:1;;	A 63% B n/a

...Expand

: 83306-66-5
N-(p-methoxybenzylidene)-p-toluidine

: C21H20O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-3-Methoxy-4-(4-methoxy-phenyl)-1-p-tolyl-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 61%

...Expand

: 40339-42-2
4-methoxy-N-[(1Z)-phenylmethylene]aniline

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-1-(4-Methoxy-phenyl)-3-phenoxy-4-phenyl-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 59%

...Expand

: 496-15-1
1-indoline

: 71001-09-7
1,2:3,4-di-O-isopropylidene-6-O-trifluoromethanesulfonyl-α-D-galactopyranose

A: 1493-13-6
trifluorormethanesulfonic acid

B: 1,2:3,4-di-O-isopropylidene-6-(indolino)-α-D-galactopyranose

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 24h; Ambient temperature;	A n/a B 57%

...Expand

: 91-21-4
1,2,3,4-tetrahydroisoquinoline

: 71001-09-7
1,2:3,4-di-O-isopropylidene-6-O-trifluoromethanesulfonyl-α-D-galactopyranose

A: 1493-13-6
trifluorormethanesulfonic acid

B: 1,2:3,4-di-O-isopropylidene-6-(1,2,3,4-tetrahydroisoquinoline)-α-D-galactopyranose

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 24h; Ambient temperature;	A n/a B 53%

...Expand

: 123525-44-0
N-(3-phenyl-2-propenylidene)-4-methoxyaniline

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-1-(4-Methoxy-phenyl)-3-phenoxy-4-((E)-styryl)-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 52%

...Expand

: 83306-67-6
p-methoxyphenylcarboxaldehyde N-(p-methoxyphenyl)imine

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-1,4-Bis-(4-methoxy-phenyl)-3-phenoxy-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 46%

...Expand

: 94612-45-0, 100239-15-4, 106318-92-7, 108908-63-0
N-(2-methyl-3-phenylprop-2-enylidene)-p-anisidine

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-1-(4-Methoxy-phenyl)-4-((E)-1-methyl-2-phenyl-vinyl)-3-phenoxy-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 45%

...Expand

: 83306-66-5
N-(p-methoxybenzylidene)-p-toluidine

: C26H22O3P(1+)*CF3O3S(1-)

A: 1493-13-6
trifluorormethanesulfonic acid

B: 791-28-6
Triphenylphosphine oxide

: (3S,4R)-4-(4-Methoxy-phenyl)-3-phenoxy-1-p-tolyl-azetidin-2-one

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃; for 0.5h; Cyclization; decomposition;	A n/a B n/a C 41%

...Expand

: 421-17-0
Trifluoromethylsulfenyl chloride

: 7722-84-1
dihydrogen peroxide

A: 372-64-5
Bis(trifluoromethyl)disulfid

B: 1493-13-6
trifluorormethanesulfonic acid

C: 421-83-0
trifluoromethane sulfonyl chloride

Conditions

Conditions	Yield
35% H2O2 soln.;	A 35% B 7% C 40%
35% H2O2 soln.;	A 35% B 7% C 40%

...Expand

: 425-75-2
trifluoromethanesulfonic acid ethyl ester

: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
at 150℃; Pyrolysis;

: 60-29-7
diethyl ether

: 333-27-7
methyl trifluoromethanesulfonate

A: 540-67-0
ethyl methyl ether

B: 425-75-2
trifluoromethanesulfonic acid ethyl ester

C: 1493-13-6
trifluorormethanesulfonic acid

Conditions

Conditions	Yield
at 80℃; unter Luftausschluss;

...Expand

: 425-75-2
trifluoromethanesulfonic acid ethyl ester

: 71-43-2
benzene

A: 1493-13-6
trifluorormethanesulfonic acid

B: 100-41-4
ethylbenzene

C: 253185-02-3
ortho-diethylbenzene

D: 781-43-1
9,10-dimethylanthracene

...Expand

: 51174-44-8
3-methyl-4-penten-1-ol

: 112238-64-9
phenylselenyl triflate

A: 1493-13-6
trifluorormethanesulfonic acid

: 109065-98-7
(2S,3R)-3-Methyl-2-phenylselanylmethyl-tetrahydro-furan

: 109065-97-6
(2S,3S)-3-Methyl-2-phenylselanylmethyl-tetrahydro-furan

Conditions

Conditions	Yield
In dichloromethane at 0℃; for 0.25h; Mechanism; Product distribution;

...Expand

: 1493-13-6
trifluorormethanesulfonic acid

: 3582-05-6
trifluoromethyl trifluoromethanesulfonate

Conditions

Conditions	Yield
With pentafluoroethanesulfonic acid anhydride at 60℃; for 4h;	100%
With phosphorus pentoxide In neat (no solvent) at 80 - 180℃; Inert atmosphere;	66%
With phosphorus pentoxide at -78 - 110℃; Inert atmosphere;	56%

: 4669-59-4
bis(diethylamino)dimethylsilane

: 1493-13-6
trifluorormethanesulfonic acid

: 155166-24-8
(diethylamino)dimethylsilyl-triflat

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 17891-70-2
bis(diethylamino)chloromethylsilane

: 1493-13-6
trifluorormethanesulfonic acid

: C6H13ClF3NO3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 18881-64-6
bis(diethylamino)dichlorosilane

: 1493-13-6
trifluorormethanesulfonic acid

: C5H10Cl2F3NO3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1624-01-7
tetrakis(dimethylamino)silane

: 1493-13-6
trifluorormethanesulfonic acid

: 155166-32-8
tris(dimethylamino)silyl triflate

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%
In toluene for 0.5h; Ambient temperature;

: 15730-66-2
tris(diethylamino)silane

: 1493-13-6
trifluorormethanesulfonic acid

: C9H21F3N2O3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 18418-65-0
methyl-tris(diethylamino)silane

: 1493-13-6
trifluorormethanesulfonic acid

: 154922-03-9
C10H23F3N2O3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%
In diethyl ether at 0℃; for 0.25h;

: 15730-69-5
SiCl(NEt2)3

: 1493-13-6
trifluorormethanesulfonic acid

: C9H20ClF3N2O3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 1048-08-4
tetraphenylsilane

: 27607-80-3
Diphenylsilicium-bis(trifluormethansulfonat)

Conditions

Conditions	Yield
In chloroform at 0℃;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 18023-34-2
bis(diethylamino)(methyl)(vinyl)silane

: C8H16F3NO3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 775-12-2
diphenylsilane

: 127808-36-0
phenylsilanyl trifluoromethanesulfonate

Conditions

Conditions	Yield
at 20℃;	100%
In toluene at 0℃; for 0.25h;	78%
In chloroform at 0℃; for 0.166667h; Yield given;
In dichloromethane at 0 - 20℃; for 0.5h;

: 1493-13-6
trifluorormethanesulfonic acid

: 1023-81-0
bis(diethylamino)(methyl)(phenyl)silane

: 154922-06-2
CH3C6H5Si(C2H5)2NCF3SO3

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%
In diethyl ether at 0℃; for 0.25h;

: 1493-13-6
trifluorormethanesulfonic acid

: 81640-85-9
N-benzoyl-N-(α-benzoylbenzyl)aniline

: 81640-37-1
2,3,4,5-tetraphenyloxazolium trifluoromethanesulphonate

Conditions

Conditions	Yield
	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 61423-53-8
vinyl-tris(diethylamino)silane

: C11H23F3N2O3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 94971-86-5
benzenetellurinic acid anhydride

: 122745-21-5
benzenetellurinyl trifluoromethanesulfonate

Conditions

Conditions	Yield
In dichloromethane for 0.5h; Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 35339-16-3
(E)-2-(3-oxo-1,3-diphenylpropylidene)-3,4-dihydronaphthalen-1(2H)-one

: 76017-15-7
2,4-diphenyl-5,6-dihydro-7,8-benzochromenylium trifluoromethanesulphonate

Conditions

Conditions	Yield
In ethanol 1.) 60 deg C, 4 h, 2.) 25 deg C, 12 h;	100%
In ethanol Heating;

: 1493-13-6
trifluorormethanesulfonic acid

: 122131-73-1
1,1,2,2-tetraphenyl-1,2-di-tert-butyl-1,2-disilane

: 155166-11-3
1,2-di-tert-butyl-1,2-diphenyldisilane-1,2-bis(triflate)

Conditions

Conditions	Yield
In toluene Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 154922-03-9
C10H23F3N2O3SSi

: 155166-33-9
C7H13F6NO6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: (Allyl-bis-diethylamino-silanyl)-diethyl-amine

: C12H25F3N2O3SSi

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: C9H21F3N2O3SSi

: C6H11F6NO6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 155166-32-8
tris(dimethylamino)silyl triflate

: C6H12F6N2O6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: C9H20ClF3N2O3SSi

: C6H10ClF6NO6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: C12H25F3N2O3SSi

: C9H15F6NO6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: C11H23F3N2O3SSi

: C8H13F6NO6S2Si

Conditions

Conditions	Yield
In diethyl ether Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 2,3-dihydro-2-(p-methoxybenzylthio)-1H-indolizinium chloride

: 2,3-dihydro-2-metcapto-1H-indolizinium trifluoromethanesulfonate

Conditions

Conditions	Yield
With trifluoroacetic acid In various solvent(s) for 1h; Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 2,3-dihydro-1-(p-methoxybenzylthio)-1H-indolizinium p-toluenesulfonate

: 2,3-dihydro-1-metcapto-1H-indolizinium trifluoromethanesulfonate

Conditions

Conditions	Yield
With trifluoroacetic acid In various solvent(s) for 1h; Ambient temperature;	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 86774-69-8
1H-2,4,6-tri-isopropyl-1,3,5-triazinium triflate

: 151-10-0
1,3-Dimethoxybenzene

: 86774-78-9
2-(2,4-dimethoxyphenyl)-2,4,6-tri-isopropyl-1,2-dihydro-1,3,5-triazinium triflate

Conditions

Conditions	Yield
In benzene for 1.5h; Ambient temperature;	100%

...Expand

: 1493-13-6
trifluorormethanesulfonic acid

: 18816-18-7
1,1,2,2,3,3-hexaphenyltrisilane

: 1,2,3-triphenyl-1,2,3-tris(trifluoromethansulfonyloxy)trisilan

Conditions

Conditions	Yield
In toluene at 0℃; for 2h;	100%

: 280-57-9
1,4-diaza-bicyclo[2.2.2]octane

: 1493-13-6
trifluorormethanesulfonic acid

: N,N'-difluoro-1,4-diazoniabicyclo<2.2.2>octane bis(triflate)

Conditions

Conditions	Yield
With fluorine In various solvent(s)	100%

: 1493-13-6
trifluorormethanesulfonic acid

: 1,3-Dibromo-1,3-di-p-tolyl-[1,3]disiletane

: Trifluoro-methanesulfonic acid 1,3-dibromo-3-trifluoromethanesulfonyloxy-[1,3]disiletan-1-yl ester

Conditions

Conditions	Yield
In diethyl ether; toluene for 1h; Ambient temperature;	100%

Trifluoromethanesulfonic acid Chemical Properties

Empirical Formula: CHF₃O₃S
Molecular Weight: 150.077 g/mol
EINECS: 216-087-5
Index of Refraction: 1.354
Density: 1.876 g/cm³
Boiling Point: 162 °C at 760 mmHg
Vapour Pressure: 1.14 mmHg at 25 °C
Melting point: -40 °C
Storage tempreture: -20 °C
Sensitive: Hygroscopic
Appearance: Clear very light yellow liquid
Structure of Trifluoromethanesulfonic acid (CAS NO.1493-13-6):

Product Category of Trifluoromethanesulfonic acid (CAS NO.1493-13-6): straight chain compounds;Organic Fluorides;Organic AcidsVolumetric Solutions;Synthetic Reagents;Titration;Volumetric Solutions

Trifluoromethanesulfonic acid Toxicity Data With Reference

p-Tolualdehyde (CAS NO.620-23-5) hasn't been listed as a carcinogen by NTP, IARC, ACGIH, or CA Prop 65. And the toxicological properties have not been fully investigated.

Trifluoromethanesulfonic acid Safety Profile

Hazard Codes: C
Risk Statements:
10: Flammable
35: Causes severe burns
21/22: Harmful in contact with skin and if swallowed
Safety Statements:
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
36/37/39: Wear suitable protective clothing, gloves and eye/face protection

Trifluoromethanesulfonic acid Specification

Trifluoromethanesulfonic acid , its cas register number is 1493-13-6. It also can be called Methanesulfonic acid, 1,1,1-trifluoro- ; and Triflic acid . It is hazardous, so the first aid measures and others should be known. Such as: When on the skin: first, should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly, get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While, it's inhaled: Remove from exposure and move to fresh air immediately. Give artificial respiration while not breathing. When breathing is difficult, give oxygen. And as soon as to get medical aid. Then you have the ingesting of the product: Wash mouth out with water, and get medical aid immediately. Notes to physician: Treat supportively and symptomatically.
In addition, p-Tolualdehyde (CAS NO.620-23-5) could be stable under normal temperatures and pressures. It absorbs moisture or water from the air, and is not compatible with strong oxidizing agents, and you must not take it with incompatible materials. And also prevent it to broken down into hazardous decomposition products: carbon monoxide, oxides of sulfur, carbon dioxide, hydrogen fluoride gas.

Product Name

Trifluoromethanesulfonic acid

Synthetic route

Trifluoromethanesulfonic acid Chemical Properties

Trifluoromethanesulfonic acid Toxicity Data With Reference

Trifluoromethanesulfonic acid Safety Profile

Trifluoromethanesulfonic acid Specification

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