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Di-tert-butyl dicarbonate - 98%, high purity , CAS No.24424-99-5

    Grade & Purity:
  • ≥98%
In stock
Item Number
D106158
Grouped product items
SKU Size
Availability
Price Qty
D106158-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$34.90
D106158-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$95.90
D106158-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$335.90

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 ≥98%
Storage Temp Store at 2-8°C
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.

43 results found

Lot Number Certificate Type Date Item
D2527061 Certificate of Analysis May 19, 2025 D106158
D2527062 Certificate of Analysis May 19, 2025 D106158
D2527060 Certificate of Analysis May 06, 2025 D106158
J2429248 Certificate of Analysis Nov 02, 2024 D106158
J2429277 Certificate of Analysis Nov 02, 2024 D106158
G2419456 Certificate of Analysis Jul 25, 2024 D106158
G2419466 Certificate of Analysis Jul 25, 2024 D106158
G2419500 Certificate of Analysis Jul 25, 2024 D106158
G2419465 Certificate of Analysis Jul 24, 2024 D106158
G2419499 Certificate of Analysis Jul 24, 2024 D106158
D2412156 Certificate of Analysis Apr 19, 2024 D106158
A2408444 Certificate of Analysis Jan 19, 2024 D106158
A2408442 Certificate of Analysis Jan 17, 2024 D106158
A2408443 Certificate of Analysis Jan 17, 2024 D106158
A2408445 Certificate of Analysis Jan 17, 2024 D106158
B2226041 Certificate of Analysis Dec 11, 2023 D106158
B2226064 Certificate of Analysis Dec 11, 2023 D106158
B2402008 Certificate of Analysis Aug 30, 2023 D106158
H2329730 Certificate of Analysis Aug 30, 2023 D106158
H2329731 Certificate of Analysis Aug 30, 2023 D106158
H2329825 Certificate of Analysis Aug 30, 2023 D106158
H2329736 Certificate of Analysis Aug 30, 2023 D106158
K2119564 Certificate of Analysis Aug 15, 2023 D106158
G2327154 Certificate of Analysis Aug 02, 2023 D106158
G2327161 Certificate of Analysis Aug 02, 2023 D106158
G2327152 Certificate of Analysis Aug 02, 2023 D106158
G2327145 Certificate of Analysis Aug 02, 2023 D106158
E2323409 Certificate of Analysis Jun 05, 2023 D106158
I2305036 Certificate of Analysis Jun 05, 2023 D106158
B2314232 Certificate of Analysis Feb 20, 2023 D106158
J2219342 Certificate of Analysis Oct 31, 2022 D106158
J2219544 Certificate of Analysis Oct 31, 2022 D106158
J2219444 Certificate of Analysis Oct 31, 2022 D106158
J2219438 Certificate of Analysis Oct 31, 2022 D106158
G2216231 Certificate of Analysis Jul 25, 2022 D106158
G2216224 Certificate of Analysis Jul 25, 2022 D106158
F2215120 Certificate of Analysis Jun 17, 2022 D106158
F2209147 Certificate of Analysis Jun 15, 2022 D106158
G2216223 Certificate of Analysis Mar 07, 2022 D106158
G2216230 Certificate of Analysis Mar 07, 2022 D106158
G2216222 Certificate of Analysis Mar 07, 2022 D106158
B2226057 Certificate of Analysis Mar 07, 2022 D106158
B2226065 Certificate of Analysis Mar 05, 2022 D106158

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Chemical and Physical Properties

Sensitivity Hygroscopic
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

Citations of This Product

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