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Di-tert-butyl dicarbonate - 99%, high purity , CAS No.24424-99-5

97 Citations COA COA
    Grade & Purity:
  • ≥99%
In stock
Item Number
D106159
Grouped product items
SKU Size
Availability
 Price Qty
D106159-25g
25g
2
$37.90
D106159-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$105.90
D106159-500g
500g
2
$369.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Amino protection (24) Deprotection (54) Derivatization (54) Protection (54) Protection and derivatization reagents (4) Tert-butoxycarbonyl (Boc)ation agent (1) tert-Butoxycarbonylation (Boc) Reagents [Protecting Reagents (1)

Basic Description

Synonyms di-t-butyldicarbonate | di-t-butyl-dicarbonate | Di-tert-butyl dicarbonate 2.0M in THF | (di-tert-butyl)dicarbonate | Di tert-butyl dicarbonate | di-t-butylpyrocarbonate | di-tert-butyl dicabonate | tBoc2O | t-Boc2O | Di-tert-butyl dicarbonate 2.0M in Dic
Specifications & Purity ≥99%
Storage Temp Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Aminomethyl allene was prepared by reaction of Boc propargyl amine with formaldehyde, diisopropylamine and copper bromide as part of a series of Bovine Plasma Amine Oxidase inactivators Protection of alcohols as Boc derivatives via Lewis acid catalysis. Reagent for the introduction of the Boc protecting group. Reagent for the preparation of Boc protected amines. Tris-Boc protected hydrazine allows preparation of Fmoc ester in a chromophoric reagent to monitor solid-phase aldehydes.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Organic carbonic acids and derivatives
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Organic carbonic acids and derivatives
Alternative Parents Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Carbonic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as organic carbonic acids and derivatives. These are compounds comprising the organic carbonic acid or a derivative thereof.
External Descriptors acyclic carboxylic anhydride

Names and Identifiers

IUPAC Name tert-butyl (2-methylpropan-2-yl)oxycarbonyl carbonate
INCHI InChI=1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3
InChIKey DYHSDKLCOJIUFX-UHFFFAOYSA-N
Smiles CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
Isomeric SMILES CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
WGK Germany 3
RTECS HT0230000
UN Number 2929
Packing Group II
Molecular Weight 218.25
Beilstein 1911173
Reaxy-Rn 1911173
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1911173&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

38 results found

Lot Number Certificate Type Date Item
D2527064 Certificate of Analysis Apr 14, 2025 D106159
D2527027 Certificate of Analysis Apr 14, 2025 D106159
D2527028 Certificate of Analysis Apr 14, 2025 D106159
L2425186 Certificate of Analysis Dec 13, 2024 D106159
L2425179 Certificate of Analysis Dec 13, 2024 D106159
K2429241 Certificate of Analysis Nov 25, 2024 D106159
K2429242 Certificate of Analysis Nov 25, 2024 D106159
J2429284 Certificate of Analysis Oct 18, 2024 D106159
G2419464 Certificate of Analysis Jul 10, 2024 D106159
G2419498 Certificate of Analysis Jul 10, 2024 D106159
G2422545 Certificate of Analysis Jul 10, 2024 D106159
F2404259 Certificate of Analysis May 24, 2024 D106159
F2404260 Certificate of Analysis May 24, 2024 D106159
D2412166 Certificate of Analysis Apr 02, 2024 D106159
D2412167 Certificate of Analysis Apr 02, 2024 D106159
D2412168 Certificate of Analysis Apr 02, 2024 D106159
D2412165 Certificate of Analysis Apr 02, 2024 D106159
A2408447 Certificate of Analysis Jan 02, 2024 D106159
A2408446 Certificate of Analysis Jan 02, 2024 D106159
A2408448 Certificate of Analysis Jan 02, 2024 D106159
A2408449 Certificate of Analysis Jan 02, 2024 D106159
L2312366 Certificate of Analysis Dec 04, 2023 D106159
L2312367 Certificate of Analysis Dec 04, 2023 D106159
H2329733 Certificate of Analysis Aug 28, 2023 D106159
E2323406 Certificate of Analysis Apr 20, 2023 D106159
E2323426 Certificate of Analysis Apr 20, 2023 D106159
E2323401 Certificate of Analysis Apr 20, 2023 D106159
G2327142 Certificate of Analysis Apr 20, 2023 D106159
B2314234 Certificate of Analysis Feb 02, 2023 D106159
J2219480 Certificate of Analysis Sep 14, 2022 D106159
J2219341 Certificate of Analysis Sep 14, 2022 D106159
D2313836 Certificate of Analysis Sep 14, 2022 D106159
F2221248 Certificate of Analysis Jul 03, 2022 D106159
G2216195 Certificate of Analysis Jun 15, 2022 D106159
G2216196 Certificate of Analysis Jun 15, 2022 D106159
G2216197 Certificate of Analysis Jun 15, 2022 D106159
G2216192 Certificate of Analysis Jun 15, 2022 D106159
B2226067 Certificate of Analysis Jan 24, 2022 D106159

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Chemical and Physical Properties

Solubility Miscible with decalin, toluene, carbon tetrachloride, tetrahydrofuran, dioxane, alcohols, acetone, acetonitrile and dimethylformamide. Immiscible with water.
Sensitivity Heat sensitive;Hygroscopic;Light sensitive;moisture sensitive
Refractive Index 1.409
Flash Point(°F) 98.6 °F
Flash Point(°C) 37℃
Boil Point(°C) 56-57 °C/0.5 mmHg
Melt Point(°C) 23°C
Molecular Weight 218.250 g/mol
XLogP3 2.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 6
Exact Mass 218.115 Da
Monoisotopic Mass 218.115 Da
Topological Polar Surface Area 61.800 Ų
Heavy Atom Count 15
Formal Charge 0
Complexity 218.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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