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ChemicalBook >> CAS DataBase List >>N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide

CAS No.
77377-52-7
Chemical Name:
N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide
Synonyms
MTBSTFA;DK398;tbstfa;MBDSTFA;DKFELEX0083;MTBSTFA=TBSTFA;MTBSTFA AND TBDMCS;DEUTERO-REGISIL-D18;MTBSTFA AND TBDMSCL;N-(tert-Butyldimethy
CBNumber:
CB7707814
Molecular Formula:
C9H18F3NOSi
Molecular Weight:
241.33
MDL Number:
MFCD00009671
MOL File:
77377-52-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:49:03
Product description Number Pack Size Price
MTBSTFA (with 1% t-BDMCS) ampule of 5 × 1?mL, (with 1% t-BDMCS), analytical standard, Cerilliant? M-108 5x1mL $82.4
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for synthesis 8.14219 1mL $71.5
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for synthesis 8.14219 5ml $226
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for GC derivatization, LiChropur?, ≥99.0% (GC) 77626 10ml $300
N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for GC derivatization, LiChropur?, ≥99.0% (GC) 77626 10X1ML $391
More product size

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide Properties

Boiling point 172-175 °C(lit.)
Density 1.036 g/mL at 25 °C(lit.)
refractive index n20/D 1.402(lit.)
Flash point 127 °F
storage temp. 2-8°C
solubility sol most aprotic organic solvents.
form Liquid
pka -1.50±0.70(Predicted)
Specific Gravity 1.023
color Clear colorless to slightly yellow
Water Solubility decomposes
Sensitive Moisture Sensitive
Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents
BRN 3606546
InChI 1S/C9H18F3NOSi/c1-8(2,3)15(5,6)13(4)7(14)9(10,11)12/h1-6H3
InChIKey QRKUHYFDBWGLHJ-UHFFFAOYSA-N
SMILES CN(C(=O)C(F)(F)F)[Si](C)(C)C(C)(C)C
CAS DataBase Reference 77377-52-7(CAS DataBase Reference)
UNSPSC Code 41116107
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
Signal word  Warning
Hazard statements  H226-H315-H319
Precautionary statements  P210-P233-P240-P241-P303+P361+P353-P305+P351+P338
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi,F
Risk Statements  10-36/37/38
Safety Statements  26-36-16-37/39-36/37/39
RIDADR  UN 1993 3/PG 3
WGK Germany  3
10-21
Hazard Note  Flammable
TSCA  No
HS Code  2931 90 00
HazardClass  3
PackingGroup  III
Storage Class 3 - Flammable liquids
Hazard Classifications Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
Limited Quantities 5.0 L (1.3 gallons) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
2
2 0

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide price More Price(78)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M-108 MTBSTFA (with 1% t-BDMCS) ampule of 5 × 1?mL, (with 1% t-BDMCS), analytical standard, Cerilliant? 77377-52-7 5x1mL $82.4 2026-04-30 Buy
Sigma-Aldrich 8.14219 N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for synthesis 77377-52-7 1mL $71.5 2026-04-30 Buy
Sigma-Aldrich 8.14219 N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for synthesis 77377-52-7 5ml $226 2026-04-30 Buy
Sigma-Aldrich 77626 N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for GC derivatization, LiChropur?, ≥99.0% (GC) 77377-52-7 10ml $300 2026-04-30 Buy
Sigma-Aldrich 77626 N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide for GC derivatization, LiChropur?, ≥99.0% (GC) 77377-52-7 10X1ML $391 2026-04-30 Buy
Product number Packaging Price Buy
M-108 5x1mL $82.4 Buy
8.14219 1mL $71.5 Buy
8.14219 5ml $226 Buy
77626 10ml $300 Buy
77626 10X1ML $391 Buy

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide Chemical Properties,Uses,Production

Chemical Properties

clear colorless to slightly yellow liquid

Physical properties

bp 168–170°C; d 1.12 g cm3.

Uses

In the presence of 1% of t-butyldimethylchlorosilane as the catalyst, N-(t-butyldimethylsilyl)-N-methyltrifluoroacetamide (BSMTFA) functions as an extremely reactive t-butyldimethylsilylating reagent for alcohols, amines, carboxylic acids, and thiols. Silylation is generally completed within 5 min at 25°C in acetonitrile. This amide is more reactive than N-(t-butyldimethylsilyl)-N-methylacetamide.
In the protection of a hydroxy group, the resultant tbutyldimethylsilyl (TBDMS) ethers are stable under the conditions for acetate saponification and hydrogenation.These silyl ethers also remain intact towards the Jones reagent and Wittig reagents. The TBDMS ethers are approx. 10 times more stable against hydrolysis than the corresponding trimethylsilyl (TMS) ethers.Selective removal of the TBDMS group can be accomplished by use of dilute acetic acid or tetra-n-butylammonium fluoride in THF at 25°C.
Silylation of ketones by use ofBSMTFAoccurs in triethylamine and DMF at 40–60°C to give the corresponding silyl enol ethers in good to excellent yields (eq 1).In addition, silyl ether formation takes place in N-hydroxysuccinimide (88% yield) and Nhydroxypyrrole (99% yield) by use of BSMTFA in THF.N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide

Uses

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide is a silylating agent used in the derivatization of various organic compounds (such as amino acids) for gas chromatogography-mass spectrometry (GC-MS) analysis.

Uses

N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-butyldimethylchlorosilane is commonly used for the preparation of N-tert-butyldimethylsilyl ethanolamines resulting from the hydrolysis of nitrogen mustards. It is also used for selective O-silylation of N,O-diacylhydroxyl amines.

Preparation

obtained in 91% yield by reaction of N-methyl-2,2,2-trifluoroacetamide (1.0 equiv) in benzene and acetonitrile (1:1 v/v) with NaH (1.0 equiv) and then with t-BuMe2SiCl (1.2 equiv) at 4°C.

Definition

ChEBI: An N-silyl compound that is N-methyltrifluoroacetamide in which the amide nitrogen is replaced by a tert-butyldimethylsilyl group.

General Description

N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide is a silylating reagent which replaces the active hydrogen with tert-Butyldimethylsilyl group. The tert-Butyldimethylsilyl derivatives are found to be more resistant to hydrolysis and stable compared to trimethylsilyl (TMS) derivatives. This reagent is suitable for GC-MS analysis since it produces mass spectra, which can be easily interpreted. It is widely used for the silylation of different alcohols, thiols, phenols, carboxylic acids, amines, and amides.

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 215)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Daken Advanced Materials Co.,Ltd
+86-2158073036 info@dakenam.com China 14026 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
SHANGHAI T&W PHARMACEUTICAL CO., LTD.
+86-021-61551413 +8618813727289 contact@trustwe.com China 5746 58
Finetech Industry Limited
+86-27-8746-5837 +8619945049750 info@finetechnology-ind.com China 9539 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52704 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418684 +8618949823763 sales@tnjchem.com China 25356 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 market18@leapchem.com China 24597 58
Golden Pharma Co., Limited
+undefined18958062155 sales@zjgoldpharm.com China 5899 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49734 58

View Lastest Price from N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide pictures 2020-01-03 N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide
77377-52-7
$1.00 1KG 99% 10000KGS Career Henan Chemical Co
MBDSTFA DEUTERO-REGISIL-D18 N-TERT-BUTYLDIME.SILYL-N-ME.TRIFLUOROACE N-TERT-BUTYLDIME.SILYL-N-ME.TRIFLUOROACE TAMIDE + 1% TBDMSCL N-(TERT-BUTYLDIMETHYLSILYL)-N-METHYL-TRI FLUOROACETAMIDE, 97+% N-(TERT-BUTYLDIMETHYLSILYL)-N-METHYLTRIF LUOROACETA N-(TERT-BUTYLDIMETHYLSILYL)-N-METHYL-TRIFLUOROACETAMIDE, W/1% TBDMSCL, >=95% N-TERT-BUTYLDIMETHYLSILYL-N-METHYL TRIFL MTBSTFA=TBSTFA SILYLATING MIXTURE FLUKA VI MTBSTFA AND TBDMCS MTBSTFA AND TBDMSCL N-METHYL(TERT-BUTYLDIMETHYLSILYL)TRIFLUOROACETAMIDE N-METHYL-N-(T-BUTYLDIMETHYLSILYL)TRIFLUOROACETAMIDE N-METHYL-N-TERT-BUTYLDIMETHYLSILYLTRIFLUOROACETAMIDE N-METHYL-N-[TERT-BUTYLDIMETHYL-SILYL]TRIFLUOROACETAMIDE AND TERT-BUTYLDIMETHYLCHLOROSILANE N-(T-BUTYLDIMETHYLSILYL)-N-METHYLTRIFLUOROACETAMIDE N-(TERT-BUTYLDIMETHYLSILYL)-N-METHYLTRIFLUORACETAMIDE N-(TERT-BUTYLDIMETHYLSILYL)-N-METHYLTRIFLUOROACETAMIDE MTBSTFA + 1% TBDMSCl, MTBSTFA+TBDMSCl, 99:1, Silylating mixture Fluka VI, N-Methyl-N-tert-butyldimethylsilyltrifluoroacetamide MTBSTFA + 1% TBDMSCl, Silylating mixture Fluka VI, N-Methyl-N-tert-butyldimethylsilyltrifluoroacetamide Acetamide, N-(1,1-dimethylethyl)dimethylsilyl-2,2,2-trifluoro-N-methyl- N-(tert-B-butyldimethylsilyl)-n-methyl- trifluoroacetamide, 98% N-Methyl-N-(tert-butyldimethylsilyl)-2,2,2-trifluoroacetamide N-(tert-Butyldimethylsilyl)-N-methyl-trifluoroacetamide,98% N-Methyl-N-[Tert-Butyld N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane,N-Methyl-N-tert-butyldimethylsilyltrifluoroacetamide, MTBSTFA + 1% TBDMSCl, MTBSTFA+TBDMSCl, 99:1, Silylatin N-(tert-Butyldimethy MTBSTFA (with 1% t-BDMCS) N-[(tert-Butyl)dimethylsilyl]-N-methyl-2,2,2-trifluoroacetamide, [Methyl(trifluoroacetyl)amino]dimethylsilane MTBSTFA + 1% TBDMSCl MTBSTFA (N-(tert-butyldiMethylsilyl)-N-METHYLTRIFLUOROACETAMIDE) MTBSTFA /1% tert-butyldiMethylchlorosilane N-tert-ButyldiMethylsilyl-N-MethyltrifluoroacetaMide with 1% tert-ButyldiMethylchlorosilane >=95% n-tert-butyldimethylsilyl-n-methyltrifluoroacetamide with 1% tert-butyldimethylchlorosilane tbstfa N-Methyl-(tert-Butydimethylsilyl)-trifluoroacetamide N-Methyl(tert-butyldimethylsilyl)trifluoroacetamide 95% N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide 99+% N-Methyl(tert-butyldimethylsilyl)trifluoroacetamide95% N-Methyl-N-(tert-butyldimethylsilyl)trifluoro- N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) MTBSTFA+TBDMSCl, 99:1 N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide >=97.0% (GC) N-[(1,1-DiMethylethyl)diMethylsilyl]-2,2,2-trifluoro-N-MethylacetaMide N-Methyl-N-(tert-butyldiMethylsilyl)-1,1,1-trifluoroacetaMide N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide MTBSTFA N-TERT-BUTYLDIMETHYLSILYL-N-METHYLTRIFLU N-[(tert-Butyl)dimethylsilyl]-N-methyltrifluoroacetamide 97% N-(tert-ButyldiMethylsilyl)-N-Methyl-trifluoroacetaMide, 98% 1GR N-(t-butyldiMethylsilyl)-N-MethyltrifluoroacetaMide with N-(t-butlydiMethylsilylchloride) [tert-butyl-(2,2,2-trifluoro-1-oxoethyl)amino]methyl-dimethylsilicon N-[tert-butyl(dimethyl)silyl]-2,2,2-trifluoro-N-methylacetamide N-(t-Butyldimethylsilyl)-N-methyltrifluoroacetamid N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide > N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (Technical Grade) DK398 DKFELEX0083
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