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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:2026-09-12 18:55:43

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)  Exclamation Mark (GHS07)
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(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC TRC-D472500-5G Dimethyl N,N-Diisopropylphosphoramidite 122194-07-4 5g $252 2026-06-03 Buy
TRC TRC-D472500-50G Dimethyl N,N-Diisopropylphosphoramidite 122194-07-4 50g $1943 2026-06-03 Buy
TRC TRC-D472500-1G Dimethyl N,N-Diisopropylphosphoramidite 122194-07-4 1g $194 2026-06-03 Buy
Biosynth FD22252 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 0.5g $150 2026-06-04 Buy
Biosynth FD22252 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 1g $150 2026-06-04 Buy
Product number Packaging Price Buy
TRC-D472500-5G 5g $252 Buy
TRC-D472500-50G 50g $1943 Buy
TRC-D472500-1G 1g $194 Buy
FD22252 0.5g $150 Buy
FD22252 1g $150 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( 47)Suppliers
Supplier Tel Email Country ProdList Advantage
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Beijing Ouhe Technology Co., Ltd 13552068683 13522913783 2355560935@qq.com China 11777 60
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
9ding chemical ( Shanghai) Limited 4009209199 sales@9dingchem.com China 18201 56
Shenzhen Nexconn Pharmatechs Ltd. 0755-89396905 admin@nexconn.com China 299 55
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
Shanghai SuperLan Chemcial Technique Centre 0-2022843681 15618226720 chaolaichem@foxmail.com China 10000 58
Zhengzhou Acme Chemical Co., Ltd. 0371-0371-55629727 13323845623 2885676761@qq.com China 9948 58
LinkChem Technology Co., Ltd. 021-58950110 13124863828 sales@linkchem.cn China 2996 58
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031 3007523370@qq.com China 40000 58

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
1KG 95%-99% 1kg; 100kg; 500kg Career Henan Chemical Co
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 Dimethyl N,N-diisopropylphosphoramidite 122194-07-4 C8H20NO2P Phosphoramidites Phosphorus Compounds Organic Building Blocks Building Blocks Organic Building Blocks Phosphoramidites Phosphorus Compounds