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Di-tert-butyl dicarbonate - 96%, high purity , CAS No.24424-99-5

97 Citations

COA

Grade & Purity:

≥96%

Cas Number: 24424-99-5
Molecular Weight: 218.25
Beilstein Registry Number: 1911173
EC Number: 246-240-1
MDL number: MFCD00008805
PubChem CID: 90495

In stock

Item Number

D106160

Grouped product items
SKU	Size	Availability	Price
D106160-25g	25g	3	$30.90
D106160-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$85.90
D106160-500g	500g	2	$299.90

View related series

Amino protection (24) Deprotection (54) Derivatization (54) Protection (54)

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	≥96%
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

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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

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.

24 results found

Lot Number	Certificate Type	Date	Item
D2527026	Certificate of Analysis	May 19, 2025	D106160
D2527025	Certificate of Analysis	May 06, 2025	D106160
G2419486	Certificate of Analysis	Jul 24, 2024	D106160
G2419497	Certificate of Analysis	Jul 24, 2024	D106160
G2419485	Certificate of Analysis	Jul 24, 2024	D106160
D2412164	Certificate of Analysis	Apr 18, 2024	D106160
H2329738	Certificate of Analysis	Aug 30, 2023	D106160
H2329734	Certificate of Analysis	Aug 30, 2023	D106160
H2329737	Certificate of Analysis	Aug 30, 2023	D106160
A2404021	Certificate of Analysis	Aug 30, 2023	D106160
G2327170	Certificate of Analysis	Aug 02, 2023	D106160
G2327149	Certificate of Analysis	Aug 02, 2023	D106160
G2308200	Certificate of Analysis	Jul 20, 2023	D106160
G2216459	Certificate of Analysis	Apr 18, 2023	D106160
G2216458	Certificate of Analysis	Apr 18, 2023	D106160
G2216191	Certificate of Analysis	Apr 18, 2023	D106160
F2202258	Certificate of Analysis	Mar 10, 2023	D106160
B2226037	Certificate of Analysis	Dec 12, 2022	D106160
J2219511	Certificate of Analysis	Oct 31, 2022	D106160
K2119559	Certificate of Analysis	Sep 09, 2022	D106160
K2119557	Certificate of Analysis	Sep 09, 2022	D106160
C2203084	Certificate of Analysis	Mar 11, 2022	D106160
C2111023	Certificate of Analysis	Jan 18, 2022	D106160
C2111028	Certificate of Analysis	Jan 18, 2022	D106160

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Chemical and Physical Properties

Solubility	Solubility in water: Practically insoluble; Very soluble in Toluene,Acetone
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 Å²
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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