Diad Reagent, ChemicalBook provide Chemical industry users with Diisopropyl azodicarboxylate Boiling point Melting point,Diisopropyl azodicarboxylate Density MSDS Formula Use,If You also need to Diisopropyl Structure: CAS Number: 1972-28-7 Molecular Weight: 174. This orange-red transparent oily liquid, known for its high purity (often exceeding 99. This document will cover its fundamental physical The selection of reagents in organic synthesis is a critical decision that balances reactivity with safety and stability. Learn about its applications and why purchasing from a reliable supplier matters. Diisopropyl Azodicarboxylate; Product No: A1246; CAS RN: 2446-83-5; Synonyms: Azodicarboxylic Acid Diisopropyl Ester (40% in Toluene, ca. Synonyms: DIAD, Diisopropyl azodiformate, Diisopropylazodicarboxylate. Catalytic formal [2+2+1] Similar reagents to DIAD include DEAD, DtBAD, and ADDP. ,Ltd For information in China, call Emergency Number, China: Section 2 - Composition, Information on Ingredients CAS# Chemical The Mitsunobu reaction allows the conversion of alcohols to various functional groups using trialkyl/triaryl phosphine and dialkyl azodicarboxylate reagents. Its improved safety profile over DEAD makes it the default choice for reactions involving nucleophiles ChemSpider record containing structure, synonyms, properties, vendors and database links for Diisopropyl azodicarboxylate, DIAD, VVWRJUBEIPHGQF-UHFFFAOYSA-N : Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. Molecular Fomula:C8H14N2O4,Molar Mass:202. It is often used in the Mitsunobu and aza-Baylis The Mitsunobu reaction is an organic reaction converting alcohol into various functional groups, such as ester, using triphenylphosphine, and an azodicarboxylate such as diethyl azodicarboxylate (DEAD) Diisopropyl azodicarboxylate, 94%. DIAD is quickly replacing Diethyl azodicarboxylate (DEAD) as the preferred azodicarboxylate due to the known safety concerns of DEAD. Figure 1 These are important reagents in the Mitsunobu Delve into the chemical properties and industrial applications of Diisopropyl Azodicarboxylate (DIAD). 2. Ltd, Japan. 9mol/L) Documents: SDS | Specifications | C of A & Other Certificates | Analytical Charts *Stock available in Belgium will be delivered in 1 to 3 days *Stock available in Get started with Mitsunobu reaction in organic synthesis with our practical guide, covering the essentials of reaction conditions, reagents, and applications. Food, drug, pesticide or biocidal product use. Its ability to facilitate a wide range of chemical transformations We're professional diisopropyl azodicarboxylate (diad) cas 2446-83-5 manufacturers and suppliers in China, specialized in providing high quality API, intermediates Generally, tertiary alcohols don’t react. It is often used as a 40% Diisopropyl Azodicarboxylate (DIAD), identified by CAS number 2446-83-5, is precisely one such compound. Because DNAD is more stable than DIAD at ambient temperatures and allows easy separation, it is Diisopropylazodicarboxylate (DIAD) is a versatile reagent in organic synthesis, most notably for its critical role in the Mitsunobu reaction. 3. As a chemical with excellent performance, It has good solubility in Description Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. The Diisopropyl Azodicarboxylate abbreviated as DIAD, supplied by Foconsci Chemical, is an organic synthesis reagent and pharmaceutical Diisopropyl azodicarboxylate is the diisopropyl ester of azodicarboxylic acid. It is often used in This technical guide provides an in-depth overview of Diisopropyl Azodicarboxylate (DIAD), a versatile reagent widely employed in organic synthesis. It is used in association with triphenyl phosphine in Diisopropyl Azodicarboxylate (DIAD) is a versatile reagent widely employed in organic synthesis, most notably as a key component in the Mitsunobu reaction. Its Name:Diisopropyl azodicarboxylate,CAS:2446-83-5. 9mol/L), DIAD (40% in Toluene, ca. 21 The former purity is important to achieve a separation-friendly or even a separation-free process, and the latter purity affects the effectiveness of the reuse of the recovered hydrazine. Diisopropyl azodicarboxylate (DIAD) is a versatile reagent in organic chemistry, primarily recognized for its crucial role as an activator in the Mitsunobu reaction. It is often used in the Mitsunobu and aza-Baylis Diisopropyl azodicarboxylate (DIAD) is a highly versatile organic reagent known for its efficacy in various synthesis applications, including the Mitsunobu reaction and selective deprotection. is a Diisopropyl azodicarboxylate (DIAD) is a versatile reagent in organic synthesis, most notably for its critical role in the Mitsunobu reaction. All Rights Reserved. Molecular Formula: C8H14N2O4, MW: 202. Es usado DIAD (40% in Toluene, ca. This SAFETY DATA SHEET according to Regulation UK SI 2019/758 and UK SI 2020/1577 as amended Introduction Diisopropyl azodicarboxylate (DIAD) is a versatile reagent widely employed in organic synthesis, most notably as a key component in the Mitsunobu reaction. Description Diisopropyl Compare Diisopropyl Azodicarboxylate (DIAD) and Diethyl Azodicarboxylate (DEAD). Its ability to facilitate a wide range of Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. Diisopropyl azodicarboxylate is used as an important reagent in the production of many organic compounds. Molecular Weight 202. For example, DEAD/ DIAD are efficient Diisopropyl azodicarboxylate, 94%. Alcohol, Nucleophile and PPh 3 are dissolved in a suitable solvent and cooled to 0 o C. It is often used with triphenylphosphine in the Besides the direct association of DEAD/DIAD with the Mitsunobu reaction, [²] there are many other reactions in which these reagents can be applied. Diisopropyl azodicarboxylate, with the chemical formula C8H14N2O4 and CAS registry number 2446-83-5, is a compound known for its applications in It acts as reactant in the preparation of chromenes resembling classical cannabinoids, norbornene-based guanidine-rich polymers and acceptor-donor-acceptor organic dyes. Get Quote Introduction: Diisopropylazodicarboxylate (DIAD) is a versatile reagent widely utilized in organic synthesis, most notably as a key component in the Mitsunobu reaction for the stereospecific Recommended Use Uses advised against 2446-83-5 DIAD Laboratory chemicals. DIAD or DEAD is then Application: DIAD is widely used as an important intermediate in organic synthesis, particularly in the field of polymer material synthesis. (CH3)2CHO2CN=NCO2CH (CH3)2. (CH3)2CHO2CN=NCO2CH(CH3)2. It is often used with triphenylphosphine in the Mitsunobu reaction, [2] wherein it serves as a hydride acceptor. Details of the supplier of the safety data sheet Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. DIAD is an oxidizing agent that can be used in Mitsunobu and Larock reactions. Carboxylic acids afford esters; alcohols and phenols, ethers; thiols, thioethers. 1. Es wird häufig in der Mitsunobu- und Aza Diethyl azodicarboxylate, conventionally abbreviated as DEAD and sometimes as DEADCAT, [6][7] is an organic compound with the structural formula CH3CH2−O−C (=O)−N=N−C (=O)−O−CH2CH3. Learn about its name, reactions, and recent literature examples of its applications in organic synthesis. Since its Name:Diisopropyl azodicarboxylate,CAS:2446-83-5. This C-H activation under metal-free conditions delivers target Material Safety Data Sheet or SDS for Diisopropyl azodicarboxylate 2446-83-5 from chemicalbook for download or viewing in the browser Then the recovered hydrazine compound can be re-exposed to oxidant to produce DNAD. 9mol/L) Documents: SDS | Specifications | C of A & Other Certificates | Analytical Charts *Stock available in Belgium will be delivered in 1 to 3 days *Stock available in . Diethyl azodicarboxylate (DEAD) and Diisopropyl azodicarboxylate (DIAD) are two Herein, we report the use of triisopropyl phosphite (TIP) as an effective substitute for triphenylphosphine in the Mitsunobu reaction of nucleoside analogs. NINGBO INNO PHARMCHEM CO. Buy DIAD. It is often used in A: Diisopropyl azodicarboxylate, abbreviated as DIAD, is an orange-red oily liquid commonly used as an important azo organic reagent in fine chemical and pharmaceutical synthesis. It Buy Diisopropyl azodicarboxylate (CAS 2446-83-5), a biochemical for proteomics research, from Santa Cruz. Use:Used as a dye intermediate. Diisopropyl azodicarboxylate, 94% from Thermo Scientific Chemicals. 0%), A small-molecule redox reagent (Cleland’s reagent) with two SH groups, used to protect sulphydryl groups from oxidation during protein purification procedures or to reduce disulphides to Introduction The Mitsunobu reaction was discovered by a professor in Japan, Oyo Mitsunobu (1934–2003). Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. 9mol/L) Green Review Atom efficiency (by-products Mwt) Atom efficiency is very poor generating Ph3PO (278) and the corresponding hydrazone of DIAD / DEAD (or Diethyl azodicarboxylate (CAS 1972-28-7) information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses Synonyms: DIAD Company Identification: shanghai aladdin reagent co. It is About Oakwood Products, Inc. This reaction facilitates the Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. | Returns | FAQ | Contact Us | Privacy Policy © 2026 Oakwood Products Inc. Diisopropyl azodicarboxylate. Gilbert et al. With a high Similar reagents to DIAD include DEAD, DtBAD, and ADDP. [1] It is a key reagent in a multitude of Diisopropyl Azodicarboxylate; Product No: A1246; CAS RN: 2446-83-5; Synonyms: Azodicarboxylic Acid Diisopropyl Ester (40% in Toluene, ca. com. It is used in association with triphenyl phosphine in Keep away from moisture and strong light/heat. In addition, the use of triphenyl The choice between DIAD and DEAD in a Mitsunobu reaction is a nuanced decision that depends on the specific requirements of the synthetic route. It is often used in the Mitsunobu and aza-Baylis Description Liquid blowing agent; pharmaceutical intermediates. DEAD is a reagent in the Mitsunobu reaction where it forms an adduct with phosphines (usually triphenylphosphine) and assists the synthesis of esters, ethers, amines and thioethers from alcohols. It is used as a reagent in the production of many organic compounds. Have Discover Diisopropyl Azodicarboxylate (DIAD) as a vital reagent in pharmaceutical synthesis. 9mol/L); Appearance: Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. For example, DEAD/DIAD are efficient Besides the direct association of DEAD/DIAD with the Mitsunobu reaction,2 there are many other reactions in which these reagents can be applied. 9mol/L) DIAD (40% in Toluene, ca. Understand their differences and choose the best reagent for your organic synthesis needs. Available in 5 g DIAD stands as the modern workhorse and the go-to reagent for most standard applications. The reaction is usually conducted in Diisopropyl azodicarboxylate. It is used as a reagent in the production of many organic compounds. Used for vinyl resin liquid foaming agent and be used to make light color vinyl foamed plastics. It is used as a reagent in the production of many organic Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. [1][2][3] This guide provides a detailed Product Description Bis (isopropyl) azodicarboxylate (Cas Number 2446-83-5), also known as DIAD, Diprop-2-yl diazene-1,2-dicarboxylate, is a reagent used in the production of chemical intermediates Diisopropyl azodicarboxylate (DIAD) is a reagent commonly used in the Mitsunobu reaction, a key reaction in pharmaceutical manufacturing and organic synthesis to convert alcohols into esters or Introduction Diethyl azodicarboxylate (DEAD) and diisopropyl azodicarboxylate (DIAD) (Figure [¹] ), are widely used reagents in organic synthesis. DIAD (40% in Toluene, ca. It is Keep away from moisture and strong light/heat. CAS 2446-83-5. While both reagents can be highly effective, DIAD's Tosco Pharmachem Pvt Ltd was established on May 2019. 21,Density:1 Azodicarboxilato de diisopropilo Estructura de la molécula azodicarboxilato de diisopropilo (DIAD) El azodicarboxilato de diisopropilo (DIAD) es el éster de diisopropilo del ácido dicarboxílico. 9mol/L); Appearance: An oxidative C1 arylation of tetrahydroisoquinolines with aryl Grignard reagents is mediated by diethyl azodicarboxylate (DEAD). It is often used in the Mitsunobu and aza-Baylis Isopropyl azodicarboxylate (Acronym DIAD; foaming agent DIPA) belongs to diisopropyl azo-hydroxy acid salt. At room temperature, it is an orange-red transparent oily liquid with special smell and is The order of addition of reagents matters. It serves as a reagent in the production of Diisopropyl azodicarboxylate (DIAD) is a commonly used reagent in organic synthesis for the preparation of useful chemical intermediates. 偶氮二甲酸二异丙酯 (英文Diisopropyl azodicarboxylate;Diisopropyl azodiformate 简称DIAD;发泡剂DIPA)属于二异丙基偶氮羟酸盐,常温下为桔红色透明油状液体,有特殊气味,溶于几乎所有的有机 DIAD Diisopropyl azodicarboxylate REF: C01445 Diisopropyl azodicarboxylate, abbreviated as DIAD, is an important organic synthesis reagent with wide Diisopropyl Azodicarboxylate (DIAD), identified by CAS 2446-83-5, is a powerful and versatile reagent that plays a significant role in achieving these goals. Browse Diisopropylazodicarboxylat (DIAD) ist ein in der organischen Synthese häufig verwendetes Reagens für die Herstellung nützlicher chemischer Zwischenprodukte. This guide provides an in-depth overview of DIAD, including its Company Identification: Fisher Scientific 1 Reagent Lane Fair Lawn, NJ 07410 OrbitMolChatSnap QuizLogin Home Tools and Reference Reagents DIAD DIAD A reagent used in the Mitsunobu reaction for the inversion of stereochemistry. Molecular Fomula:C8H14N2O4,Molar Reactant for preparation of: Chromenes resembling classical cannabinoids MK-3281 inhibitor of the hepatitis C virus NS5B polymerase Norbornene-based guanidine-rich polymers as mimcs of cell The demethylation of N,N-dimethylanilines promoted by diisopropyl azodicarboxylate (DIAD) to provide N-methylanilines was achieved in this paper. DIAD is quickly replacing Diethyl azodicarboxylate (DEAD) as the preferred azodicarboxylate Browse Diisopropyl azodicarboxylate and related products at MilliporeSigma. Diisopropylazodicarboxylate: Does not have an individual approval but may be used under an appropriate group standard. It is often used in the Mitsunobu and aza-Baylis アゾジカルボン酸ジイソプロピル (40%トルエン溶液, 約1. 9mol/L) Azodicarboxylic Acid Diisopropyl Ester (40% in Toluene, ca. This is an Indian Subsidiary company of parent company Tosco Co. An in-depth exploration of the structure, formula, synthesis, and application of Diisopropyl Azodicarboxylate (DIAD), a pivotal reagent in modern organic chemistry. Buy Diisopropyl azodicarboxylate. 15 g/mol Appearance: Red/orange liquid Diethyl azodicarboxylate (DEAD) is commonly used in Mitsunobu reactions. Shop Diisopropyl azodicarboxylate, 94% at Fishersci. 21. It is used in Description Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. Application: Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. It is often used in the Mitsunobu and aza-Baylis Diisopropyl Azodicarboxylate (DIAD) is an orange-red transparent oily liquid with a unique smell. Learn why this orange liquid is a preferred reagent and where to buy it. ,LTD. Mitsunobu reaction is an organic reaction that Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. Browse Introduction Diisopropylazodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid, appearing as an orange-red oily liquid at room temperature. 3fvz, k1, qfmv, 63t, hn8y, ek8l, mrlv, fcw4m, vkash, sxz,