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DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE

CAS No.
122194-07-4
Chemical Name:
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE
Synonyms
dimethyl diisopropylphosphoramidite;DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE;DIMETHYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE;Dimethyl N,N-diisopropylphosphoramidite >=95.0% (GC);Dimethyl N,N-diisopropylphosphoramidite;Phosphoramidous acid, N,N-bis(1-methylethyl)-, dimethyl ester
CBNumber:
CB8440943
Molecular Formula:
C8H20NO2P
Molecular Weight:
193.22
MDL Number:
MFCD00153505
MOL File:
122194-07-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:07
Product description Number Pack Size Price
Dimethyl N,N-diisopropylphosphoramidite D472500 5g $185
Dimethyl N,N-diisopropylphosphoramidite FD22252 10g $275
Dimethyl N,N-diisopropylphosphoramidite 97% AK186440 5g $293
Dimethyl N,N-diisopropylphosphoramidite 97% OR963457 5g $363
Dimethyl N,N-diisopropylphosphoramidite Z8605 10g $549

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Properties

Boiling point 54 °C10 mm Hg(lit.)
Density 0.840 g/mL at 20 °C(lit.)
refractive index n20/D 1.420(lit.)
Flash point 100 °C
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform (Sparingly), Ethyl Acetate (Sparingly)
form Oil
color Clear Colourless
Stability Moisture Sensitive
InChI 1S/C8H20NO2P/c1-7(2)9(8(3)4)12(10-5)11-6/h7-8H,1-6H3
InChIKey KXUMNSXPAYCKPR-UHFFFAOYSA-N
SMILES COP(OC)N(C(C)C)C(C)C
UNSPSC Code 12352116

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
10-21
HS Code  2929 90 00
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
0 1

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC D472500 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 5g $185 2021-12-16 Buy
Biosynth Carbosynth FD22252 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 10g $275 2021-12-16 Buy
Ark Pharm AK186440 Dimethyl N,N-diisopropylphosphoramidite 97% 122194-07-4 5g $293 2021-12-16 Buy
Apolloscientific OR963457 Dimethyl N,N-diisopropylphosphoramidite 97% 122194-07-4 5g $363 2021-12-16 Buy
AK Scientific Z8605 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 10g $549 2021-12-16 Buy
Product number Packaging Price Buy
D472500 5g $185 Buy
FD22252 10g $275 Buy
AK186440 5g $293 Buy
OR963457 5g $363 Buy
Z8605 10g $549 Buy

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Chemical Properties,Uses,Production

Uses

A useful reagent for the efficient phosphorylation of alcohols.

reaction suitability

reaction type: Phosphorylations

Synthesis

Methanol

67-56-1

DIISOPROPYLPHOSPHORAMIDOUS DICHLORIDE

921-26-6

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE

122194-07-4

General procedure for the synthesis of dimethyl N,N-diisopropylphosphoramidite amide from methanol and dichloro-N,N-diisopropylphosphoramidite: firstly, the yellow solution obtained from the reaction was subjected to rotary evaporation, followed by the direct addition of 47 mL (325 mmol, 32.9 g) of triethylamine and 250 mL of tetrahydrofuran, and stirring of the mixture to obtain a yellow suspension. Anhydrous methanol 13 mL (322 mmol, 10.3 g) was prepared in a dropping funnel, and methanol was slowly added dropwise to the reaction system over a period of 20 min under nitrogen protection and an ice-salt bath, and the dropping funnel was washed with 150 mL of tetrahydrofuran. Upon completion of the dropwise addition, the reaction mixture was transformed into a white suspension. The ice bath was removed and stirring was continued for 2 h. The reaction was then allowed to stand for a few minutes and diafiltration was performed to obtain a yellow liquid containing a light pink solid. The solid was washed with a small amount of tetrahydrofuran. The tetrahydrofuran was removed by rotary evaporation. The product was dissolved in 10 mL of 5% sodium bicarbonate solution and extracted three times with 20 mL of dichloromethane, the organic phases were combined, the dichloromethane was removed by rotary evaporation, and finally a reduced pressure distillation was performed to collect 78 stable fractions. A colorless liquid and a white solid were observed in the condenser tube, which were identified as the same substance, and the collections could be combined to give a final yield of 16.68 g with 42% yield.

References

[1] Journal of the Chemical Society. Perkin Transactions 2, 1998, # 7, p. 1621 - 1628
[2] Patent: CN102977145, 2017, B. Location in patent: Paragraph 0184; 0185

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Preparation Products And Raw materials

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Suppliers

Global( 45)Suppliers
Supplier Tel Email Country ProdList Advantage
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View Lastest Price from DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE pictures 2019-12-25 DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE
122194-07-4
US $0.01 / KG 1KG 95%-99% 1kg; 100kg; 500kg Career Henan Chemical Co
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE DIMETHYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE Dimethyl N,N-diisopropylphosphoramidite >=95.0% (GC) Phosphoramidous acid, N,N-bis(1-methylethyl)-, dimethyl ester dimethyl diisopropylphosphoramidite Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 C8H20NO2P Phosphoramidites Phosphorus Compounds Organic Building Blocks Building Blocks Organic Building Blocks Phosphoramidites Phosphorus Compounds