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Diisopropyl azodicarboxylate, 94%, Thermo Scientific Chemicals
Catalog number: L10386.14
25 g, Each
Thermo Scientific Chemicals
Diisopropyl azodicarboxylate, 94%, Thermo Scientific Chemicals
Catalog number: L10386.14
25 g, Each
Quantity
Catalog number: L10386.14
also known as L10386-14
Price (EUR)
39,51 Online price
43,90
Each
Quantity
-
Chemical Identifiers
CAS
2446-83-5
IUPAC Name
N-{[(propan-2-yloxy)carbonyl]imino}(propan-2-yloxy)formamide
Molecular Formula
C8H14N2O4
InChI Key
VVWRJUBEIPHGQF-UHFFFAOYSA-N
SMILES
CC(C)OC(=O)N=NC(=O)OC(C)C
Specifications
Specification SheetAppearance (Color)
Clear, orange to reddish brown
Form
Liquid
Assay (GC)
≥ 92.0%
Description
Diisopropyl azodicarboxylate is used as an important reagent in the production of many organic compounds. It is used in association with triphenyl phosphine in Mitsunobu reaction of alcohols, acids and amides. It acts as reactant in the preparation of chromenes resembling classical cannabinoids, norbornene-based guanidine-rich polymers and acceptor-donor-acceptor organic dyes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Diisopropyl azodicarboxylate is used as an important reagent in the production of many organic compounds. It is used in association with triphenyl phosphine in Mitsunobu reaction of alcohols, acids and amides. It acts as reactant in the preparation of chromenes resembling classical cannabinoids, norbornene-based guanidine-rich polymers and acceptor-donor-acceptor organic dyes.
Solubility
Immiscible with water.
Notes
Store in cool place. Light sensitive. Incompatible with strong oxidizing agents, strong bases, alcohols and metallic salts. Decomposes violently at or above: 100 0C.
Diisopropyl azodicarboxylate is used as an important reagent in the production of many organic compounds. It is used in association with triphenyl phosphine in Mitsunobu reaction of alcohols, acids and amides. It acts as reactant in the preparation of chromenes resembling classical cannabinoids, norbornene-based guanidine-rich polymers and acceptor-donor-acceptor organic dyes.
Solubility
Immiscible with water.
Notes
Store in cool place. Light sensitive. Incompatible with strong oxidizing agents, strong bases, alcohols and metallic salts. Decomposes violently at or above: 100 0C.
RUO – Research Use Only
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Safety and Handling
Classification of the substance or mixture
CLP classification - Regulation(EC) No 1272/2008
Skin Corrosion/Irritation
Category 2
Serious Eye Damage/Eye Irritation
Category 2
Specific target organ toxicity - (single exposure)
Category 3
Specific target organ toxicity - (repeated exposure)
Category 2
Chronic aquatic toxicity
Category 2
Label Elements
Signal Word
Warning
Hazard Statements
H315 - Causes skin irritation
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
H373 - May cause damage to organs through prolonged or repeated exposure
H411 - Toxic to aquatic life with long lasting effects
Precautionary Statements
P280 - Wear protective gloves/protective clothing/eye protection/face protection
P302 + P352 - IF ON SKIN: Wash with plenty of soap and water
P304 + P340 - IF INHALED: Remove person to fresh air and keep comfortable for breathing
P312 - Call a POISON CENTER or doctor if you feel unwell
P332 + P313 - If skin irritation occurs: Get medical advice/attention
P337 + P313 - If eye irritation persists: Get medical advice/attention