Dicarbonic acid bis(1,1-dimethylethyl)ester Pyrocarbonic acid di-tert-butyl ester 24424-99-5 in stock factory Di-tert-butyl pyrocarbonate

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Di-tert-butyl dicarbonate CAS 24424-99-5  in stock factory  Di-tert-butyl pyrocarbonate

24424-99-5

CAS 24424-99-5

Di-tert-butyl pyrocarbonate; Dicarbonic acid bis(1,1-dimethylethyl)ester; Pyrocarbonic acid di-tert-butyl ester

tert-butoxycarbonyl anhydride

Product Name:    Di-tert-butyl dicarbonate
Synonyms:    (BOC)2O;(BOC)2O FLUKA;BOC;BOC ANHYDRIDE;tert-butyldicarbonate;PYROCARBONIC ACID DI-TERT-BUTYL ESTER;RARECHEM TB OC 0001;(t.-Boc)2O
CAS:    24424-99-5
MF:    C10H18O5
MW:    218.25
EINECS:    246-240-1
Product Categories:    Miscellaneous Reagents;Amino Acid Derivatives;Starting Raw Materials & Intermediates;Organics;N-Protecting Reagents;Biochemistry;Peptide Synthesis;Protection & Derivatization Reagents (for Synthesis);Protective Reagents (Peptide Synthesis);Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Boc-Amino acid series;Pharmaceutical Intermediates;DIBOC;-
Mol File:    24424-99-5.mol
Di-tert-butyl dicarbonate Structure
Di-tert-butyl dicarbonate Chemical Properties
Melting point     23 °C(lit.)
Boiling point     65-67 °C
density     0.95 g/mL at 25 °C(lit.)
refractive index     n20/D 1.409(lit.)
Fp     99 °F
storage temp.     2-8°C
form     Low Melting Crystalline Solid
color     White
Specific Gravity    0.950
Water Solubility     Miscible with decalin, toluene, carbon tetrachloride, tetrahydrofuran, dioxane, alcohols, acetone, acetonitrile and dimethylformamide. Immiscible with water.
Sensitive     Moisture Sensitive
BRN     1911173
InChIKey    DYHSDKLCOJIUFX-UHFFFAOYSA-N
CAS DataBase Reference    24424-99-5(CAS DataBase Reference)
EPA Substance Registry System    Dicarbonic acid, bis(1,1-dimethylethyl) ester(24424-99-5)
Safety Information
Hazard Codes     T+,T,F,Xi,F+
Risk Statements     11-19-26-36/37/38-43-10-40
Safety Statements     16-26-28-36/37-45-7/9-37/39-24-36/37/39-33
RIDADR     UN 2929 6.1/PG 1
WGK Germany     3
RTECS     HT0230000
F     4.4-10-21
Autoignition Temperature    460 °C
Hazard Note     Flammable/Irritant/Very Toxic
TSCA     Yes
HazardClass     6.1
PackingGroup     I
HS Code     29209010
Toxicity    LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 2000 mg/kg
MSDS Information
Provider    Language
Di-tert-butyl dicarbonate    English
SigmaAldrich    English
ACROS    English
ALFA    English
Di-tert-butyl dicarbonate Usage And Synthesis
Chemical Properties    White to off-white microcrystalline powder
Chemical Properties    Di-tert-butyl dicarbonate (Boc2O) and di-tert-butyl tricarbonate ((BocO)2CO)  have been used as amine carbonylating reagents to obtain linear or branched aliphatic isocyanates.
most of the known methods for transforming amines into isocyanates are not mild enough and furnish undefined products as a result of uncontrolled side reactions. However, 4-dimethylaminopyridine (DMAP)-catalyzed reaction with activated carbonates as C1 building blocks constitutes a convenient laboratory method for the phosgene-free isocyanation of amines. A procedure has been described whereby alkyl- and arylamines are converted into isocyanates in high yields by reaction with activated carbonates (for example, di-tert-butyl dicarbonate, Boc2O) in the presence of a catalytic amount of a nucleophilic nitrogen base at room temperature.
Di-tert-butyl dicarbonate (Boc2O) is a widely used reagent for introducing protecting groups in peptide synthesis. The reaction of substituted anilines with Boc2O in the presence of a stoichiometric amount of 4-dimethylaminopyridine (DMAP) in an inert solvent (acetonitrile, dichloromethane, ethyl acetate, tetrahydrofuran, toluene) at room temperature leads to aryl isocyanates in almost quantitative yields within 10 min.
Uses    Reagent commonly used in organic chemistry for the introduction of the BOC protecting group.
Uses    reagent for t-BOC-protected amines
Uses    Reagent for the preparation of Boc-amino acids and peptides in high yields.
Purification Methods    Melt the ester by heating at ~35o, and distil it in a vacuum. If IR and NMR ( 1810m 1765 cm-1 , in CCl4 1.50 singlet) suggest very max impure, then wash with an equal volume of H2O containing citric acid to make the aqueous layer slightly acidic, collect the organic layer and dry it over anhydrous MgSO4 and distil it in a vacuum. [Pope et al. Org Synth 57 45 1977, Keller et al. Org Synth 63 160 1985, Grehn et al. Angew Chem 97 519 1985.] FLAMMABLE.
Di-tert-butyl dicarbonate Preparation Products And Raw materials
Preparation Products    N-Boc-D-proline-->BOC-L-Isoleucine -->5-[N-(TERT-BUTOXYCARBONYL)AMINO]-2-CHLOROPYRIDINE-->TERT-BUTYL 4-(5-FORMYL-4-METHYL-1,3-THIAZOL-2-YL)PIPERIDINE-1-CARBOXYLATE-->1-Boc-4-cyanopiperidine-->TERT-BUTYL 4-(4-FORMYL-1,3-THIAZOL-2-YL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE-->6-TERT-BUTOXYCARBONYLAMINO-PYRIDINE-2-CARBOXYLIC ACID-->1-TERT-BUTYL 6-METHYL 3-FORMYL-1H-INDOLE-1,6-DICARBOXYLATE-->(S)-N-Boc-allylglycine-->TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE-->2-(2,2-DIMETHYL-PROPIONYLAMINO)-ISONICOTINIC ACID-->1-Boc-piperazine-->Spermidine-->TERT-BUTYL 3-(4-AMINO-2,6-DICHLOROPHENOXY)PROPYLCARBAMATE-->3-TERT-BUTOXYCARBONYLAMINO-ISONICOTINIC ACID-->6-BOC-HYDRAZINONICOTINIC ACID-->4-BOCAMINO-NICOTINIC ACID-->(S)-(-)-1-tert-Butoxycarbonyl-3-aminopyrrolidine-->(R)-PIPERAZINE-2-CARBOXYLIC ACID-->(3-HYDROXYMETHYL-PYRIDIN-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER-->6-(BOC-AMINO)-HEXYL BROMIDE-->N-1-BOC-N-4-CBZ-2-PIPERAZINECARBOXYLIC ACID T-BUTYL ESTER-->4-ALLYL-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER-->1-BOC-PIPERAZINE-->TERT-BUTYL 4-(HYDROXYMETHYL)PYRIDIN-2-YLCARBAMATE-->1-BOC-4-HYDROXY-4-(HYDROXYMETHYL)-PIPERIDINE-->(S)-(-)-1-Boc-2-pyrrolidinemethanol-->TERT-BUTYL 4-FORMYL-2-METHOXYPHENYL CARB ONATE, 99-->3-[(N-(TERT-BUTYLOXYCARBONYL)AMINO)METHYL]PYRIDINE-->tert-Butyl N-(2-bromoethyl)carbamate-->N-Boc-N,N-bis(2-chloroethyl)amine-->4-CHLORO-(N-BOC)ANILINE 97-->TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE-->4-(BOC-AMINOMETHYL)PYRIDINE-->N-BOC-piperidine-4-carboxylic acid-->1-(4-PYRIDYLMETHYL)PIPERAZINE-->N,N-DIMETHYL-2-PIPERAZIN-1-YL-ACETAMIDE-->1-Boc-3-oxopiperazine-->TERT-BUTYL 4-(METHOXYCARBONYL)PYRIDIN-2-YLCARBAMATE
Raw materials    Tetrahydrofuran-->Carbon tetrachloride-->CARBON DIOXIDE-->Potassium tert-butanolate-->1,8-Diazabicyclo[5.4.0]undec-7-ene-->N-OCTANE

Product Name:	Di-tert-butyl dicarbonate
Synonyms:	(BOC)2O;(BOC)2O FLUKA;BOC;BOC ANHYDRIDE;DI-T-BUTYL DICARBONATE;DI-T-BUTYL PYROCARBONATE;DI-TERT-BUTYL PYROCARBONATE;DI-TERT-BUTYL DICARBONATE
CAS:	24424-99-5
MF:	C10H18O5
MW:	218.25
EINECS:	246-240-1
Product Categories:	Amino Acid Derivatives;Starting Raw Materials & Intermediates;Organics;N-Protecting Reagents;Biochemistry;Peptide Synthesis;Protection & Derivatization Reagents (for Synthesis);Protective Reagents (Peptide Synthesis);Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Boc-Amino acid series;Miscellaneous Reagents;Pharmaceutical Intermediates
Mol File:	24424-99-5.mol

Name        Di-tert-butyl dicarbonate
Synonyms        Di-tert-butyl pyrocarbonate; Dicarbonic acid bis(1,1-dimethylethyl)ester; Pyrocarbonic acid di-tert-butyl ester
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Molecular Structure        CAS # 24424-99-5, Di-tert-butyl dicarbonate, Di-tert-butyl pyrocarbonate, Dicarbonic acid bis(1,1-dimethylethyl)ester, Pyrocarbonic acid di-tert-butyl ester
Molecular Formula        C10H18O5
Molecular Weight        218.25
CAS Registry Number        24424-99-5
EINECS        246-240-1
 
Properties
Density        0.949
Melting point        22-24 ºC
Boiling point        56-57 ºC (0.5 torr)
Refractive index        1.4075-1.4095
Flash point        37 ºC

Di-tert-butyl dicarbonate is a reagent widely used in organic synthesis. This carbonate ester reacts with amines to give N-tert-butoxycarbonyl or so-called Boc derivatives. These derivatives do not behave as amines, which allows certain subsequent transformations to occur that would have otherwise affected the amine functional group. The Boc can later be removed from the amine using acids. Thus, Boc serves as a protective group, for instance in solid phase peptide synthesis. It is unreactive to most bases and nucleophiles, allowing for an orthogonal Fluorenylmethyloxycarbonyl chloride (FMOC-Cl) protection.
Basic Info
Chemical Name    tert-butoxycarbonyl anhydride
Synonyms    
DBDC;
DIBOC,BOC;
Dibutyldicarbonate;
Pyrocarbonic Acid Di-tert-butyl Ester;
Di-tert-butyl Pyrocarbonate;
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CAS No.    24424-99-5
Molecular Formula    C10H18O5
Molecular Weight    218.24700
PSA    61.83000
LogP    2.87320
Properties
Appearance & Physical State    White to off-white microcrystalline powder
Density    0.95 g/mL at 25 °C(lit.)
Boiling Point    65-67 °C
Melting Point    23 °C(lit.)
Flash Point    99 °F
Refractive Index    n20/D 1.409(lit.)
Storage Condition    2-8°C
Safety Info
RTECS    HT0230000
Hazard Class    6.1
Safety Statements    S16; S26; S28
HS Code    29209010
Packing Group    I
WGK Germany    3
RIDADR    UN 2929 6.1/PG 1
Risk Statements    R11; R19; R26; R36/37/38; R43; R10
Hazard Codes    T+; Xi; F+
Caution Statement    P210; P280; P304 + P340 + P310; P305 + P351 + P338 + P310; P370 + P378; P403 + P235
Signal Word    Danger
Symbol    GHS02, GHS05, GHS06
Hazard Declaration    H225; H315; H317; H318; H330; H335; H336
Synthesis Route

tert-butoxycarbonyl anhydride