ChemicalBook > CAS DataBase List > Di-tert-butyl N,N-diisopropylphosphoramidite

Di-tert-butyl N,N-diisopropylphosphoramidite

Product Name
Di-tert-butyl N,N-diisopropylphosphoramidite
CAS No.
137348-86-8
Chemical Name
Di-tert-butyl N,N-diisopropylphosphoramidite
Synonyms
DI-TERT-BUTYL DIISOPROPYLPHOSPHORAMIDITE;N,N-diisopropylphosphoraMidite;DI-TERT-BUTYL-N,N-DIISOPROPYLPHOSPHORAMIDITE;13748-86-8;di-tert-butyl diisopropylphosphoramide;DIISOPROPYL DI-TERT-BUTYLPHOSPHORAMIDITE;DI-T-BUTYL N,N-DIISOPROPYLPHOSPHORAMIDITE;Di-tert-butoxy(diisopropylamino)phosphine;Di-tert-butyl diisopropylphosphoramidoite;Di-tert-butyl N,N-Diisopropylphosphoramidine
CBNumber
CB2747336
Molecular Formula
C14H32NO2P
Formula Weight
277.38
MOL File
137348-86-8.mol
More
Less

Di-tert-butyl N,N-diisopropylphosphoramidite Property

Boiling point:
85-90 °C/0.2 mmHg (lit.)
Density 
0.879 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.444(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
4.90±0.70(Predicted)
form 
Liquid
color 
Clear colorless
BRN 
4858847
Stability:
Moisture Sensitive
InChI
InChI=1S/C14H32NO2P/c1-11(2)15(12(3)4)18(16-13(5,6)7)17-14(8,9)10/h11-12H,1-10H3
InChIKey
YGFLCNPXEPDANQ-UHFFFAOYSA-N
SMILES
P(N(C(C)C)C(C)C)(OC(C)(C)C)OC(C)(C)C
CAS DataBase Reference
137348-86-8(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-23
HS Code 
29349990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
419362
Product name
Di-tert-butyl N,N-diisopropylphosphoramidite
Purity
95%
Packaging
1g
Price
$57.4
Updated
2025/07/31
Sigma-Aldrich
Product number
419362
Product name
Di-tert-butyl N,N-diisopropylphosphoramidite
Purity
95%
Packaging
5g
Price
$161
Updated
2025/07/31
TCI Chemical
Product number
D4211
Product name
Di-tert-butyl N,N-Diisopropylphosphoramidite
Purity
>98.0%(N)
Packaging
1g
Price
$44
Updated
2025/07/31
TCI Chemical
Product number
D4211
Product name
Di-tert-butyl N,N-Diisopropylphosphoramidite
Purity
>98.0%(N)
Packaging
5g
Price
$160
Updated
2025/07/31
TRC
Product number
D429400
Product name
Di-t-butylN,N-Diisopropylphosphoramidite
Packaging
50g
Price
$720
Updated
2021/12/16
More
Less

Di-tert-butyl N,N-diisopropylphosphoramidite Chemical Properties,Usage,Production

Chemical Properties

Clear Colourless Liquid

Uses

Di-tert-butyl N,N-diisopropylphosphoramidite is a general reagent to introduce tert-butyl-protected phosphate groups. It is commonly used in phosphorylation of biomolecules. It can also be used in the synthesis of phosphoramidate-linked glycoconjugates.

Uses

A phosphinane derivative with immunomodulating activity.

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

Synthesis

921-26-6

75-65-0

137348-86-8

General procedure for the synthesis of di-tert-butyl N,N-diisopropylphosphoramidite from dichloro-N,N-diisopropylphosphoramidite and tert-butyl alcohol: tert-butyl alcohol (3.7 g, 4.7 mL, 50 mmol, 2.0 eq.) and triethylamine (5.6 g, 7.7 mL, 55 mmol, 2.2 eq.) were prepared under anhydrous conditions by dissolving them in anhydrous ether (20 mL) as a solution. This solution was slowly added to a solution of dichloro-N,N-diisopropylphosphoramidite (5.0 g, 25 mmol) in anhydrous ethyl ether (5 mL) while keeping the reaction temperature below 0°C. The reaction temperature was kept below 0°C for a few minutes. After the addition was complete (about 15 minutes), the reaction mixture was slowly warmed to room temperature and stirring was continued for 3 hours. Upon completion of the reaction, the aqueous phase was separated by adding 5% aqueous sodium bicarbonate solution (10 mL) for quenching. The organic phase was washed sequentially with 5% aqueous sodium bicarbonate (2 x 10 mL) and saturated aqueous sodium chloride (25 mL), then dried over anhydrous sodium sulfate, filtered and concentrated to give a clarified oily residue. The target product, N,N-diisopropylphosphoramidite di-tert-butyl ester, was purified by vacuum distillation as a clear oil (4.3 g, 63% yield). The boiling point of the product was 56-57 °C (0.05 mmHg).1H-NMR (300 MHz, CDCl3) δ 1.17 (d, J = 6.0 Hz, CH(CH3)2), 1.35 (s, 18H, 2 × C(CH3)3), 3.53-3.68 (m, 2 × CH(CH3)2); 13C-NMR (125 MHz, CDCl3) δ 24.5 (s, 18H, 3.53-3.68 (m, 2 × CH(CH3)2)); and 13C-NMR (125 MHz, CDCl3) δ 24.0 (m, 2 × C(CH3)3). CDCl3) δ 24.21 (d, JPC = 7.73 Hz), 31.06 (d, JPC = 9.75 Hz), 43.09 (d, JPC = 13.88 Hz), 74.50 (d, JPC = 9.75 Hz); 31P-NMR (202 MHz, CDCl3) δ 130.0 (s).

References

[1] Patent: US7018987, 2006, B1. Location in patent: Page/Page column 9
[2] Journal of the Chemical Society. Perkin Transactions 2, 1998, # 7, p. 1621 - 1628
[3] Phosphorus, Sulfur and Silicon and Related Elements, 2000, vol. 164, p. 277 - 291

Di-tert-butyl N,N-diisopropylphosphoramidite Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Di-tert-butyl N,N-diisopropylphosphoramidite Suppliers

Shanghai YuLue Chemical Co., Ltd.
Tel
021-60345187 13671753212
Fax
021-34702061
Email
lzz841106@aliyun.com
Country
China
ProdList
10263
Advantage
55
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15838
Advantage
69
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9310
Advantage
66
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11035
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
7247
Advantage
62
Sci General Material & Chemical Ltd
Tel
021-58388037;21-58388037 13472507714
Email
35177634@qq.com;1589045147@qq.com
Country
China
ProdList
803
Advantage
55
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Shanghai Raise Chemical Technology Co.,Ltd
Tel
+86-021-50935922
Fax
+86-021-33847795
Country
China
ProdList
7865
Advantage
55
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9979
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
Sinocompound Catalysts Co., Ltd.
Tel
0512-67216630 67216634
Fax
0512-56316689
Email
sales@sinocompound.com
Country
China
ProdList
271
Advantage
64
Hunan HuaTeng Pharmaceutical Co., Ltd.,
Tel
400-8592883
Fax
0731-82251112
Email
sales@huatengsci.com
Country
China
ProdList
5872
Advantage
58
Xinxiang Runyu Material Co., Ltd.
Tel
166-166-37336996 15690792173
Fax
0373-7759608
Email
chenxi.song@runvmat.com
Country
China
ProdList
285
Advantage
55
Cool Pharm, Ltd
Tel
021-60455363 18019463053
Fax
50966098
Email
sales@coolpharm.com
Country
China
ProdList
12346
Advantage
58
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51395
Advantage
80
Shanghai Send Pharmaceutical Technology Co., Ltd.
Tel
021-58088081 Q2635253576
Fax
QQ3382968513
Email
hailey@shsendpharm.com
Country
China
ProdList
2081
Advantage
55
Nanjing Vital Chemical Co., Ltd.
Tel
025-87193546 18652950785
Fax
025-87193546
Email
chemweiao@163.com
Country
China
ProdList
9021
Advantage
60
ShangHai Siyan Biological Technology Co., Ltd.
Tel
021-50908862,442785678,326799392 18721037013
Fax
021-50908862
Email
siyansales@126.com
Country
China
ProdList
9627
Advantage
58
Shanghai Haozhixiang Biotechnology Co., Ltd
Tel
526763801 13301653310
Fax
+86-21-51619052
Email
526763801@qq.com
Country
China
ProdList
9287
Advantage
55
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
Shanghai Changyan Chem & Tech Co., Ltd.
Tel
021-20242659 18930833303
Fax
+86 (21) 2024-2659
Email
Sales@changyanchem.cn
Country
China
ProdList
5001
Advantage
55
parabiochem
Tel
025-83453382-8005
Fax
025-83453382
Email
sale@parabiochem.com
Country
China
ProdList
9595
Advantage
55
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Shanghai Kangman Biological Technology Co., Ltd.
Tel
18800375331
Fax
021-50908862
Email
kangmansales@163.com
Country
China
ProdList
7570
Advantage
55
Taian Jiaye Biotechnology Co.Ltd
Tel
13127280945
Email
285424065@qq.com
Country
China
ProdList
9976
Advantage
55
Shandong Ono Chemical Co., Ltd.
Tel
0539-6362799 20)
Fax
0539-6362799(To 20)
Country
China
ProdList
9998
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19800
Advantage
60
LinkChem Technology Co., Ltd.
Tel
021-58950110 13124863828
Fax
021-20922272
Email
sales@linkchem.cn
Country
China
ProdList
3000
Advantage
58
Jiaxing Deyi Chemical Co., Ltd.
Tel
86-0573-85866609 13325730825
Fax
0573-85866609
Email
945717149@qq.com
Country
China
ProdList
8595
Advantage
58
Shanghai Yongzhi chemical-Technology Co., Ltd.
Tel
021-60944093 18516153908 13917602471
Fax
021-60944093
Email
mianyanghaodao@aliyun.com
Country
China
ProdList
411
Advantage
58
Capot Chemical Co.,Ltd.
Tel
+86-(0)57185586718; +8613336195806
Fax
+86-571-85864795
Email
sales@capot.com
Country
China
ProdList
29735
Advantage
60
Aikon International Limited
Tel
025-58851090 15955137747
Fax
(6)02557626880
Email
sales01@aikonchem.com
Country
China
ProdList
15949
Advantage
58
Shanghai Haohong Pharmaceutical Co., Ltd.
Tel
400-8210725 400821072
Fax
021-58955996
Email
malulu@leyan.com
Country
China
ProdList
25000
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
4009004166/18616739031 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52687
Advantage
58
Shanghai Thoreco Novel Material Co. Ltd
Tel
021-34202258 17317865669;
Email
Sales@thoreco.com
Country
China
ProdList
183
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57422
Advantage
58
Shanghai Boyi Chemical Technology Co., Ltd.
Tel
021-54096810
Fax
021-65329886
Email
sales@birchchem.com
Country
China
ProdList
104
Advantage
58
Henan Alfa Chemical Co., Ltd
Tel
+8615838112936
Email
alfa10@alfachem.cn
Country
China
ProdList
12921
Advantage
58
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
+86-0551-65418684 +8618949823763
Fax
0086-551-65418684
Email
sales@tnjchem.com
Country
China
ProdList
25356
Advantage
58
Dayang Chem (Hangzhou) Co.,Ltd.
Tel
+86-0571-88938639 +8617705817739
Fax
+86-571-88938652,+86-571- 88492614
Email
info@dycnchem.com
Country
China
ProdList
52846
Advantage
58
Chemwill Asia Co.,Ltd.
Tel
86-21-51086038
Fax
86-21-51861608
Email
chemwill_asia@126.com
Country
CHINA
ProdList
23912
Advantage
58
Shanghai TenSus Biotechnology Co., Ltd.
Tel
021-50895067 18616507272
Fax
021-50895067
Email
tensus@163.com
Country
China
ProdList
8073
Advantage
58
Guangdong Wengjiang Chemical Reagent Co., Ltd.
Tel
0751-2886766 13927870850
Fax
0751-2886756
Email
3001267247@qq.com
Country
China
ProdList
9941
Advantage
58
More
Less

View Lastest Price from Di-tert-butyl N,N-diisopropylphosphoramidite manufacturers

R&D Scientific Inc.
Product
Di-tert-butyl N,N-diisopropylphosphoramidite 137348-86-8
Price
US $2200.00/Kg
Min. Order
1Kg
Purity
97
Supply Ability
500 Kg
Release date
2024-07-11
Shaanxi Dideu Medichem Co. Ltd
Product
Di-tert-butyl N,N-diisopropylphosphoraMidite 137348-86-8
Price
US $1.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20 tons
Release date
2020-01-16
Career Henan Chemical Co
Product
Di-tert-butyl N,N-diisopropylphosphoramidite 137348-86-8
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1
Release date
2018-08-06

137348-86-8, Di-tert-butyl N,N-diisopropylphosphoramiditeRelated Search:


  • DI-T-BUTYL N,N-DIISOPROPYLPHOSPHORAMIDITE
  • DI-TERT-BUTYL DIISOPROPYLPHOSPHORAMIDITE
  • DI-TERT-BUTYL-N,N-DIISOPROPYLPHOSPHORAMIDITE
  • DI-TERT-BUTYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE
  • N,N-Bis(1-methylethyl)phosphoramidous Acid Bis(1,1-dimethylethyl)ester
  • N,N-BisisopropylphosphoraMidous acid bis(tert-butyl) ester
  • N,N-diisopropylphosphoraMidite
  • Di-tert-butyl N,N-diisopropylphosphoraMidite 95%
  • 13748-86-8
  • Phosphoramidous acid,N,N-bis(1-methylethyl)-, bis(1,1-dimethylethyl) ester
  • di-tert-butyl diisopropylphosphoramide
  • Di-tert-butoxy(diisopropylamino)phosphine
  • Di-tert-butylN,N-Diisopropylphosphoramidite&gt
  • DIISOPROPYL DI-TERT-BUTYLPHOSPHORAMIDITE
  • N-Di-tert-butoxyphosphanyl-N-isopropyl-propan-2-amine
  • Di-tert-butyl diisopropylphosphoramidoite
  • Di-tert-butyl N,N-Diisopropylphosphoramidine
  • N-[bis[(2-methylpropan-2-yl)oxy]phosphanyl]-N-propan-2-ylpropan-2-amine
  • Bis(1,1-dimethylethyl) N,N-bis(1-methylethyl)phosphoramidite
  • Bis(tert-butyl) N,N-bis(1-methylethyl)phosphoramidite
  • Di-<i>tert</i>-butyl <i>N,N</i>-diisopropylphosphoramidite
  • Bis(tert-butyl) N,N-bis(isopropyl)phosphoramidite
  • N. N-diisopropylphosphoramidite di tert butyl ester
  • 137348-86-8
  • 13748-86-8
  • C14H32NO2P
  • CH32CH2NPOCCH332
  • Catalysis and Inorganic Chemistry
  • Phosphorus Compounds
  • Phosphine Ligands
  • Phosphorylating and Phosphitylating Agents
  • Catalysis and Inorganic Chemistry
  • Phosphine Ligands
  • Phosphorus Compounds
  • Phospholipids - 13C & 2H