DMT-dC(bz) Phosphoramidite CAS 102212-98-6 Purity ≥98.0% (HPLC) DNA Phosphoramidites

Short Description:

Chemical Name: DMT-dC(bz) Phosphoramidite

CAS: 102212-98-6

Purity: ≥98.0% (HPLC)

Purity: ≥98.0% (31P-NMR)

Appearance: White to Off-White Powder

DNA Phosphoramidites for Oligonucleotide Synthesis

Contact: Dr. Alvin Huang

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E-Mail: alvin@ruifuchem.com

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DNA Phosphoramidites:

DMT-dC(bz) Phosphoramidite	CAS 102212-98-6
DMT-dT Phosphoramidite	CAS 98796-51-1
DMT-dA(Bz) Phosphoramidite	CAS 98796-53-3
DMT-dG(Ib) Phosphoramidite	CAS 93183-15-4
DMT-dC(ac) Phosphoramidite	CAS 154110-40-4
DMT-dG(dmf) Phosphoramidite	CAS 330628-04-1

102212-98-6 - Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer of DMT-dC(bz) Phosphoramidite (CAS: 102212-98-6) with high quality. DNA Phosphoramidites for Oligonucleotide Synthesis. Used for Molecular Biology Research.
Ruifu Chemical can provide worldwide delivery, competitive price, excellent service.
Purchase DMT-dC(bz) Phosphoramidite or other products, please contact us by e-mail: alvin@ruifuchem.com

102212-98-6 - Chemical Properties:

Chemical Name	DMT-dC(bz) Phosphoramidite
Synonyms	5'-O-DMT-N4-Benzoyl-2'-Deoxycytidine 3'-CE Phosphoramidite; dC (N-Bz) Phosphoramidite; dC (Bz) CE-Phosphoramidite; DNAC-Phosphoramidite; N4-Benzoyl-2'-Deoxy-5'-O-DMT-Cytidine 3'-CE Phosphoramidite; N-Benzoyl-5'-O-(4,4'-Dimethoxytrityl)-2'-Deoxycytidine-3'-(2-Cyanoethyl-N,N-Diisopropyl)phosphoramidite; N-Benzoyl-5'-O-[bis(4-Methoxyphenyl)(phenyl)methyl]-3'-O-[(2-Cyanoethoxy)(diisopropylamino)phosphino]-2'-Deoxycytidine
Stock Status	In Stock, Commercial Production
CAS Number	102212-98-6
Molecular Formula	C46H52N5O8P
Molecular Weight	833.92 g/mol
Melting Point	>84℃(dec.)
Density	1.23 at 20℃
Store Under Inert Gas	Store Under Inert Gas
Sensitive	Moisture Sensitive, Heat Sensitive
Storage Temperature	Sealed in Dry, Store at -20℃, Protect From Light, Stored Under Nitrogen
Shipping Conditions	Shipped Under Ambient Temperature For Short Term
Expiration Date	12 Months From Date of Receipt
COA & MSDS	Available
Origin of Product	Shanghai, China
Product Categories	DNA Phosphoramidites
Caution	Not For Human or Veterinary Use. For Research Use Only.
Brand	Ruifu Chemical

102212-98-6 - Specifications:

Items	Specifications	Results
Appearance	White or Off-White Powder	White Powder
Water Content	≤0.30% (Karl Fischer)	Conforms
Purity / Analysis Method	≥98.0% (HPLC)	99.5%
Purity / Analysis Method	≥98.0% (31P-NMR)	Conforms
1H NMR Spectrum	Conforms to Structure	Conforms
LC-MS	Conforms to Structure	Conforms
Conclusion	The product has been tested and complies with the given specifications

102212-98-6 - Package/Storage/Shipping:

Package: 1g/10g/50g/100g/1kg/10kg/bulk. Amber glass screw cap vial or white plastic bottle.
Storage Condition: Keep the container tightly closed. Sealed in dry, store in freezer, store at -20℃, protect from light, stored under nitrogen. Keep away from sunshine; avoid fire and heat sources; avoid moisture.
Shipping: Deliver to worldwide by air, by FedEx / DHL Express. Provide fast and reliable delivery.

102212-98-6 - 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

102212-98-6 - 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 Assurance? Strict 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.

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

Factory Audit? Factory audit welcome. Please make an appointment in advance.

MOQ? No MOQ. Small order is acceptable.

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

Transportation? By Express (FedEx, DHL), by Air, by Sea.

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

Custom Synthesis? Can provide custom synthesis services to best fit your research needs.

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

102212-98-6 - Risk and Safety:

Safety Description	24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	2934.99.9001

102212-98-6 - Introduction:

DMT-dC(bz) Phosphoramidite (CAS: 102212-98-6) is a nucleoside phosphoramidite with a fluorine on the 2' position and a cytidine capped with a benzoyl functional group.
DMT-dC(bz) Phosphoramidite is an important chemical reagent used in the synthesis of oligonucleotides for a variety of scientific applications. It is a derivative of the nucleoside dC and a phosphoramidite, which is a type of phosphite. This compound is used in the synthesis of DNA and RNA molecules and is particularly useful in the construction of oligonucleotide libraries. It is also used in the synthesis of modified oligonucleotides, such as those containing modified bases or modified linkages.

102212-98-6 - Scientific Research Applications:

DMT-dC(bz) Phosphoramidite (CAS: 102212-98-6) is used in a variety of scientific research applications. It is used in the synthesis of oligonucleotide libraries, which are used for a variety of purposes such as gene expression analysis, gene function analysis, and drug discovery. DMT-dC(bz) Phosphoramidite is also used in the synthesis of modified oligonucleotides, such as those containing modified bases or modified linkages. These modified oligonucleotides are useful for a variety of applications, such as gene silencing and gene editing.
DMT-dC(bz) Phosphoramidite can be used to study the interaction of DNA with drugs, including anticancer drugs, antibiotics, and antivirals.
DMT-dC(bz) Phosphoramidite can be used in the development of DNA-based sensors for the detection of environmental toxins, pathogens, and other analytes.

102212-98-6 - Mechanism of Action:

The mechanism of action of DMT-dC(bz) Phosphoramidite (CAS: 102212-98-6) is based on the formation of a phosphoramidite linkage between a nucleoside and a phosphite. In the presence of a base and a catalyst, a phosphite reacts with a nucleoside to form a phosphoramidite. The phosphoramidite is then reacted with a protecting group, which is then removed to yield the desired product.

102212-98-6 - Biochemical and Physiological Effects:

DMT-dC(bz) Phosphoramidite (CAS: 102212-98-6) is a chemical reagent and does not have any direct biochemical or physiological effects. However, it is used in the synthesis of oligonucleotides, which can have a variety of biochemical and physiological effects. For example, oligonucleotides can be used to regulate gene expression, which can lead to changes in cellular physiology.

102212-98-6 - Advantages and Limitations for Lab Experiments:

The main advantage of using DMT-dC(bz) Phosphoramidite in lab experiments is that it is a versatile reagent that can be used in the synthesis of a variety of oligonucleotides. DMT-dC(bz) Phosphoramidite is also relatively easy to use and can be used to synthesize oligonucleotides with modified bases or linkages. The main limitation of using this reagent is that it is relatively expensive, which can limit its use in some experiments.

102212-98-6 - Future Directions:

The use of DMT-dC(bz) Phosphoramidite in the synthesis of oligonucleotides has a number of potential future directions. These include the development of more efficient and cost-effective methods for the synthesis of modified oligonucleotides, the development of new applications for oligonucleotides, such as gene editing and gene silencing, and the development of new methods for the synthesis of oligonucleotides with modified linkages. Additionally, further research into the mechanism of action of this reagent could lead to new applications and improved synthesis methods.