Quality Level
Assay
≥98.0% (GC)
form
solid or liquid
refractive index
n20/D 1.409 (lit.)
bp
56-57 °C/0.5 mmHg (lit.)
mp
23 °C (lit.)
density
0.95 g/mL at 25 °C (lit.)
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
InChI
1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3
InChI key
DYHSDKLCOJIUFX-UHFFFAOYSA-N
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General description
Automated Boc protection and deprotection can be done using Synple Automated Synthesis Platform (SYNPLE-SC002), Boc protection cartridges ((SYNPLE-B001), (SYNPLE-B002), and Boc deprotection cartridges (SYNPLE-B011)
Application
- An azobenzene amino acid(aa).
- N-tert-butoxycarbonyl-3,4-methylenedioxymethamphetamine (t-BOC-MDMA) from MDMA.
It can also be used as a reagent:
- To introduce acid-labile Boc-protecting group in amino acids, peptides, and proteins.
- To prepare styrene derivatives by Heck olefination of aromatic carboxylic acids in the presence of a Pd catalyst.
- To synthesize oxazolidin-2-ones and imidazolidin-2-ones by isocyanation of 1,2-aminoalcohols and 1,2-diamines using DMAP as a catalyst.
- In the preparation of N-tert-butoxycarbonyl-3,4-methylenedioxymethamphetamine (t-Boc-MDMA) from MDMA.
- For the conversion of amines to corresponding isocyanates, carbamates, and urea derivatives.
- In the N-BOC-ylation of amides.
- In the N-BOC-ylation of sensitive compounds under non-aqueous conditions.
Warning
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 1 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
98.6 °F - closed cup
Flash Point(C)
37 °C - closed cup
Personal Protective Equipment
Regulatory Information
Certificates of Analysis (COA)
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705578-5MG-PW
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1000309185
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Aldrich Products
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