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Diphenylphosphoryl azide

Product Name
Diphenylphosphoryl azide
CAS No.
26386-88-9
Chemical Name
Diphenylphosphoryl azide
Synonyms
DPPA;DIPHENYL PHOSPHORAZIDATE;DIPHENYLPHOSPHONIC AZIDE;DIPHENYL AZIDOPHOSPHATE;diphenylphophoryl azide;Diphenylphosphorazindate(DPPA);Diphenyphosphoryl azide;Diphenyl azide phosphate;phosphorazidicacid,diphenylester;PS-DPPA
CBNumber
CB3404964
Molecular Formula
C12H10N3O3P
Formula Weight
275.2
MOL File
26386-88-9.mol
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Diphenylphosphoryl azide Property

Boiling point:
157 °C/0.17 mmHg (lit.)
Density 
1.277 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.551(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Acetonitrile (Slightly), Chloroform (Slightly), Ethyl Acetate (Sparingly)
form 
Liquid
Specific Gravity
1.277
color 
slightly yellow
Water Solubility 
insoluble
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
2058967
Stability:
Stable. Incompatible with acids, strong oxidizing agents.
InChIKey
SORGEQQSQGNZFI-UHFFFAOYSA-N
CAS DataBase Reference
26386-88-9(CAS DataBase Reference)
NIST Chemistry Reference
Diphenylphosphoryl azide(26386-88-9)
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Safety

Hazard Codes 
T
Risk Statements 
23/24/25-36/37/38
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3278 6.1/PG 2
WGK Germany 
3
3-10
Hazard Note 
Toxic/Keep Cold
TSCA 
No
HazardClass 
6.1
PackingGroup 
III
HS Code 
29299000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

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

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
178756
Product name
Diphenyl phosphoryl azide
Purity
97%
Packaging
5g
Price
$29.1
Updated
2024/03/01
Sigma-Aldrich
Product number
178756
Product name
Diphenyl phosphoryl azide
Purity
97%
Packaging
5kg
Price
$2480
Updated
2024/03/01
TCI Chemical
Product number
D1672
Product name
Diphenylphosphoryl Azide
Purity
>97.0%(GC)
Packaging
5g
Price
$25
Updated
2024/03/01
TCI Chemical
Product number
D1672
Product name
Diphenylphosphoryl Azide
Purity
>97.0%(GC)
Packaging
25g
Price
$67
Updated
2024/03/01
Alfa Aesar
Product number
A12124
Product name
Diphenylphosphonic azide, 97%
Packaging
5g
Price
$24.65
Updated
2024/03/01
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Diphenylphosphoryl azide Chemical Properties,Usage,Production

Chemical Properties

Diphenylphosphoryl azide (DPPA) is a colorless or pale yellow liquid which boils at 134-136 °C/0.2 mmHg, and it will be stable at room temperature under shading. It is non-explosive just like the other phosphorazidate. When DPPA is stored at room temperature for a long time, it might be slowly and partially hydrolyzed with moisture in air to produce diphenyl phosphate and toxic explosive hydrazoic acid. In this case, it will be recommended to use after washing DPPA with aqueous sodium hydrogen carbonate followed by drying.

Uses

Diphenylphosphoryl azide (DPPA or diphenyl phosphorazidate, (PhO)2P(O)N3) is a very toxic and potentially explosive organic compound. DPPA has been found to be effective for a variety of organic reactions as a versatile synthetic reagent. It is widely used in synthesis of other organic compounds especially as a reagent for the synthesis of peptides by virtue of its reactions with carboxylic acids leading to either the urethane or the amide.

Application

Diphenylphosphoryl azide (DPPA) is a well-known azide reagent used in peptide couplings, Curtius rearrangements, and Mitsunobu inversions—is often encountered in pharmaceutical process development because it enables the most direct route to a desired product. Diphenylphosphonic azide acts as a reagent for the synthesis of peptides and phosphoramidates by reacting with amines. It is also used in the preparation of oligosaccharides linked with carbamate and urea bonds utilizing modified Curtis rearrangement. It is involved in pseudohalogen replacement of the azido group by treatment with nucleophilic reagents, such as water, butanol, ammonia, and various amines. Further, it is used as a hydroazidation catalyst for preparation of organoazides.

Preparation

Diphenylphosphoryl azide (DPPA) is easily prepared in high yield by the reaction of the corresponding chloride with sodium azide in acetone. Combination of sodium azide and 18-crown-6 in the same reaction was reported, and the use of a quaternary ammonium salt as a phase-transfer catalyst in a biphasic phase of water and an organic solvent was also reported to be effective, as shown in Scheme 3.

Diphenyl Phosphorazidate (DPPA) - More Than Three Decades Later
Takayuki Shioiri
Graduate School of Environmental and Human Sciences, Meijo University

Reactions

Diphenylphosphoryl azide, originally developed by Yamada in 1972, has shown significant synthetic versatility, being used in isocyanate synthesis, especially in the Curtius rearrangement, stereospecific conversion of alcohol into azide, as a coupling reagent in macrolactamization[4], in allylic amine synthesis, and in aziridination reactions. Diphenylphosphoryl azide, also called DPPA, diphenyl phosphorazidate or phosphoric acid diphenyl ester azide, is a colorless liquid with high boiling point (157 ??C/0.17 mmHg), and can be easily prepared by the reaction between diphenylphosphoryl chloride and sodium azide in acetone in high yield. The Waldvogel group developed a reliable protocol for the large-scale (100 g) synthesis of DPPA, including purification by reduced-pressure distillation (Picture 1). A polymer-supported form of the reagent has also been developed using phenol resin by the Taylor group.

Mechanism of action

Diphenyl phosphoryl azide is used in the aziridination of olefins catalyzed by colbalt-tetraphenylporphyrin. It is also used as the activating agent in the preparation of macrocyclic lactams and of an aldose reductase inhibitor.

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Diphenylphosphoryl azide Suppliers

Suzhou Highfine Biotech Co., Ltd
Tel
0512-68311833 13962195826
Email
wuhao@highfine.com
Country
China
ProdList
1405
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58
Taizhou Yichuan Chemical Industry Co., Ltd
Tel
0576-88652780 13906597690
Fax
13666895861
Email
879507987@qq.com
Country
China
ProdList
23
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58
Changzhou DongChen Pharmaceutical Co., Ltd.
Tel
0519-88995800 13815038136
Fax
0519-88995808
Country
China
ProdList
62
Advantage
55
HEZE DIJADE CHEMCAL CORPORATION
Tel
0530-7157019 18678572026
Email
3109950577@qq.com
Country
China
ProdList
18
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58
NANJING YUANMING CHEMICAL CO., LTD.
Tel
025-57885806 18951785526
Email
3075076875@qq.com
Country
China
ProdList
27
Advantage
58
Henan Wanxiang Chemical Industry Co.,Ltd.
Tel
0371-56669001 13949088811
Fax
0371-56669008
Email
Sales@58chem.cn
Country
China
ProdList
285
Advantage
58
Nanjing Yihua Biotechnology Co., Ltd
Tel
15952064210
Email
184982398@qq.com
Country
China
ProdList
296
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58
Nanjing Yili Biotechnology Co., Ltd.
Tel
18795999647
Email
2853992905@qq.com
Country
China
ProdList
8134
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58
Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Fax
+86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2208
Advantage
55
Shanghai Tuolei Chemical Reagents Co., Ltd.
Tel
86-021-50318510
Fax
021-58650104
Country
China
ProdList
69
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55
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View Lastest Price from Diphenylphosphoryl azide manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Diphenylphosphoryl azide 26386-88-9
Price
US $60.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000kg/week
Release date
2024-05-23
hebei hongtan Biotechnology Co., Ltd
Product
Diphenylphosphoryl azide 26386-88-9
Price
US $30.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
2000kg
Release date
2024-05-17
Hebei Weibang Biotechnology Co., Ltd
Product
Diphenylphosphoryl azide 26386-88-9
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-25

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