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Safety Information

79408

Sigma-Aldrich

Phosphazene base P1-t-Bu

≥97.0% (GC)

Synonym(s):

tert-Butylimino-tris(dimethylamino)phosphorane, N′-tert-Butyl-N,N,N′,N′,N″,N″-hexamethylphosphorimidic triamide

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About This Item

Empirical Formula (Hill Notation):
C10H27N4P
CAS Number:
81675-81-2
Molecular Weight:
234.32
Beilstein:
4178783
MDL number:
MFCD00145111
UNSPSC Code:
12352001
PubChem Substance ID:
57652790
NACRES:
NA.22

Quality Level

100

Assay

≥97.0% (GC)

form

liquid

functional group

amine

SMILES string

CN(C)P(N(C)C)(N(C)C)=NC(C)(C)C

InChI

1S/C10H27N4P/c1-10(2,3)11-15(12(4)5,13(6)7)14(8)9/h1-9H3

InChI key

YRNOSHBJMBLOSL-UHFFFAOYSA-N

Application

Phosphazene Bases: a Family of Extremely Strong, Non-Ionic, Non-Charged Nitrogen–Bases

Other Notes

Sterically hindered, neutral nitrogen base with similar basicity as BEMP (Cat. No. 20025); Base for dehydrating carbamate anions to isocyanates with POCl3 or P4O10

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H314,H340,H350

Hazard Classifications

Carc. 1B - Eye Dam. 1 - Muta. 1B - Skin Corr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

79408-VAR:
79408-5ML:4548174007761
79408-25ML:4548174007754
79408-1ML:
79408-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH5640
BCBW5899
BCBT9517
BCBM1851V
BCBH2522V

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T.E. Waldman et al.
Journal of the Chemical Society. Chemical Communications, 957-957 (1994)
R. Schwesinger et al
Angewandte Chemie (International Edition in English), 105, 1420-1420 (1994)
Lan-Fang Hu et al.
Molecules (Basel, Switzerland), 25(2) (2020-01-16)
The copolymerization of biorenewable succinic anhydride (SA) with propylene oxide (PO) is a promising way to synthesize biodegradable aliphatic polyesters. However, the catalytic systems for this reaction still deserve to be explored because the catalytic activity of the reported catalysts

Articles

Phosphazene Bases

Phosphazene base reagents are available as monomeric (P1 and BEMP), dimeric (P2), and tetrameric (P4) bases with different side chains to control their sterical hindrance.

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