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Merck
CN

365963

Di-tert-butyl N,N-diethylphosphoramidite

technical grade, 93%

Synonym(s):

Bis(1,1-dimethylethyl) N,N-diethylphosphoramidite, Di-tert-butyl diethylphosphoramidite

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About This Item

Linear Formula:
(C2H5)2NP[OC(CH3)3]2
CAS Number:
117924-33-1
Molecular Weight:
249.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24862597
MDL number:
MFCD00134307
Beilstein/REAXYS Number:
4175262
Assay:
93%
Form:
liquid

Key Documents

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Product Name

Di-tert-butyl N,N-diethylphosphoramidite, technical grade, 93%

InChI

1S/C12H28NO2P/c1-9-13(10-2)16(14-11(3,4)5)15-12(6,7)8/h9-10H2,1-8H3

SMILES string

CCN(CC)P(OC(C)(C)C)OC(C)(C)C

InChI key

KUKSUQKELVOKBH-UHFFFAOYSA-N

grade

technical grade

assay

93%

form

liquid

refractive index

n20/D 1.434 (lit.)

bp

39-41 °C/0.3 mmHg (lit.)

density

0.896 g/mL at 25 °C (lit.)

functional group

amine

storage temp.

2-8°C

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

172.4 °F - closed cup

flash_point_c

78 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH2070
MKCC3888
MKBP7763V
MKBJ2137V
MKAA4094

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Calcium phosphate nanoparticles: colloidally stabilized and made fluorescent by a phosphate-functionalized porphyrin.
Ganesan K, et al.
Journal of Materials Chemistry, 18(31), 3655-3661 (2008)
H Mostafavi et al.
Biomedical peptides, proteins & nucleic acids : structure, synthesis & biological activity, 1(5), 255-260 (1995-01-01)
Based on the global phosphorylation approach, a selective synthesis of (Ser10-phosphatidyl)-urodilatin (phosphourodilatin), which contains 32 amino acid residues and a disulfide loop is described. The peptide was assembled stepwise on a polyethyleneglycol-polystyrene support using Fmoc-chemistry. The phosphorylation was performed on-resin
J W Perich et al.
Bioorganic & medicinal chemistry, 4(2), 143-150 (1996-02-01)
The seven phosphopeptide derivatives based on the native -NEYTA- sequence of the pp60src protein kinase family, Asn-Glu-Tyr(P)-Ser-Ala, Ala-Glu-Tyr(P)-Ser-Ala, Ala-Ser-Tyr(P)-Ser-Ala, Ala-Ser(P)-Tyr-Ser-Ala, Ala-Thr-Tyr(P)-Ser-Ala, Ala-Thr(P)-Tyr-Ser-Ala and Ala-Ser(P)-Tyr(P)-Ser-Ala, were prepared in good yield using the "global' "phosphite-triester' phosphorylation method. The peptide resins were assembled
D Dunn et al.
The Journal of biological chemistry, 271(1), 168-173 (1996-01-05)
Yersinia protein-tyrosine phosphatase substrates have been synthesized employing an expedient methodology that incorporates phosphorylated non-amino acid residues into an active site-directed peptide. While the peptidic portion of these compounds serves an enzyme targeting role, the nonpeptidic component provides a critical

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