TCFH CAS 94790-35-9 Purity >99.0% (HPLC) Factory Coupling Reagents

Short Description:

Chemical Name: TCFH 

CAS: 94790-35-9

Purity: >99.0% (HPLC)

White to Off-White Crystalline Powder

Coupling Reagents, High Quality 

Contact: Dr. Alvin Huang

Mobile/Wechat/WhatsApp: +86-15026746401

E-Mail: alvin@ruifuchem.com


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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer of TCFH (CAS: 94790-35-9) with high quality. Ruifu Chemical supplys a series of protecting reagents and coupling reagents. Ruifu can provide worldwide delivery, competitive price, small and bulk quantities available. Purchase TCFH, Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name N,N,N',N'-Tetramethylchloroformamidinium Hexafluorophosphate
Synonyms TCFH; Chloro-N,N,N',N'-Tetramethylformamidinium Hexafluorophosphate; N-[Chloro(dimethylamino)methylene]-N-Methyl-Methanaminium Hexafluorophosphate; Tetramethylchloroformamidinium Hexafluorophosphate
Stock Status In Stock, Mass Production
CAS Number 94790-35-9 
Molecular Formula C5H12ClF6N2P 
Molecular Weight 280.58 g/mol
Melting Point 99.0~108.0℃ 
Density 1.58 
Sensitive Moisture Sensitive, Heat Sensitive 
Storage Temp.  Cool & Dry Place (2~8℃) 
COA & MSDS Available
Category   Coupling Reagents 
Brand Ruifu Chemical

Specifications:

Items Inspection Standards Results
Appearance White to Off-White Crystalline Powder Complies      
Melting Point 99.0~108.0℃ 102.4~103.6℃
Loss on Drying <0.50% 0.15% 
Purity / Analysis Method >99.0% (HPLC)  99.9% 
Infrared Spectrum Conforms to Structure Complies      
Proton NMR Spectrum Conforms to Structure Complies      
Conclusion The product has been tested & complies with the given specifications

Package/Storage/Shipping:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry (2~8℃) warehouse away from incompatible substances. Protect from light and moisture.
Shipping: Deliver to worldwide by FedEx / DHL Express. Provide fast and reliable delivery. 

Advantages:

Sufficient Capacity: Sufficient facilities and technicians

Professional Service: One stop purchasing service

OEM Package: Custom package and label available

Fast Delivery: If within stock, three days delivery guaranteed

Stable Supply: Maintain reasonable stock    

Technical Support: Technology solution available

Custom Synthesis Service: Ranged from grams to kilos

High Quality: Established a complete quality assurance system

FAQ:

How to Purchase? Please contact Dr. Alvin Huang: sales@ruifuchem.com or alvin@ruifuchem.com 

15 Years Experience? We have more than 15 years of experience in the manufacture and export of a wide range of high quality pharmaceutical intermediates or fine chemicals.

Main Markets? Sell to domestic market, North America, Europe, India, Korea, Japanese, Australia, etc.

Advantages? Superior quality, affordable price, professional services and technical support, fast delivery.

Quality AssuranceStrict quality control system. Professional equipment for analysis include NMR, LC-MS, GC, HPLC, ICP-MS, UV, IR, OR, K.F, ROI, LOD, MP, Clarity, Solubility, Microbial limit test, etc.

SamplesMost products provide free samples for quality evaluation, shipping cost should be paid by customers.

Factory AuditFactory audit welcome. Please make an appointment in advance.

MOQ? No MOQ. Small order is acceptable.

Delivery Time? If within stock, three days delivery guaranteed.

TransportationBy Express (FedEx, DHL), by Air, by Sea.

Documents? After sales service: COA, MOA, ROS, MSDS, etc. can be provided.

Custom SynthesisCan provide custom synthesis services to best fit your research needs.

Payment TermsProforma invoice will be sent first after confirmation of order, enclosed our bank information. Payment by T/T (Telex Transfer), PayPal, Western Union, etc. 

94790-35-9 - Risk and Safety:

Risk Codes
R36/37/38 - Irritating to eyes, respiratory system and skin.
R40 - Limited evidence of a carcinogenic effect
Safety Description
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S22 - Do not breathe dust.
WGK Germany 3
FLUKA BRAND F CODES 3-10-21

Application:

N,N,N',N'-Tetramethylchloroformamidinium Hexafluorophosphate (TCFH) (CAS: 94790-35-9), coupling reagent for peptide synthesis and starting material for preparing other coupling reagents. TCFH is a good non-hygroscopic peptide synthesis coupling reagent. As a general activation reagent of solid phase chemistry, TCFH mainly promotes the formation of carboxylic acid amine derivatives rather than amide in the coupling process of amino acids. It is very useful for the coupling of very hindered amino acids, and has the characteristics of simple and convenient synthesis process and long shelf life.
TCFH is a safe, affordable reagent for ester and difficult amide synthesis.
TCFH as a reagent has several advantages beside being economical:
– Due to is high coupling potency, it might be used in reactions previously only accomplished using carbodiimide-mediated couplings, extending in this manner its application for the formation of esters, diacyl amides and acylation of non-reactive amines
– It is solid, reasonably stable compound, when stored around 0°C
– Using the widely available coupling additives the chemist can find optimal reagent ratio to balance between the product yield and the side reactions including epimerization. 

Preparation:

Over a period of 2 minutes, to 1,1,3,3-Tetramethylurea (2.5 mL, 21 mmol)/10 mL toluene solution a small portion of oxalyl chloride (2.0 mL, 23 mmol) was added while the reaction mixture was stirred at ice-water bath temperature. After stirring at room temperature for 18 hours, the reaction mixture was concentrated under reduced pressure to a volume of about 5 mL and the resulting precipitate was collected by filtration. The collected solid was dissolved in about 20 mL of water and then treated with potassium hexafluorophosphate (3.8g, 21 mmol)/50 mL of aqueous solution while the mixture was vigorously stirred at room temperature, to obtain a white precipitate. The precipitate was collected by filtration and dried under vacuum. The solid was then treated with about 8 mL of acetone and filtered to remove insoluble material. The resulting filtrate was added in small portions to 60 mL of diethyl ether with vigorous stirring at room temperature. The desired product was collected by filtration and dried under vacuum to give 4.5g (76%).

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