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DIAMMONIUM HYDROGEN PHOSPHATE-15N2 is a nitrogen and phosphorus-rich compound that features two nitrogen atoms labeled with the isotope 15N. This isotopic labeling provides a unique advantage for tracking and tracing nitrogen uptake and utilization in plants and soil, making it a valuable tool for research and agricultural applications.

287488-11-3

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287488-11-3 Usage

Uses

Used in Agricultural Industry:
DIAMMONIUM HYDROGEN PHOSPHATE-15N2 is used as a fertilizer to enhance soil fertility and promote plant growth. Its high nitrogen and phosphorus content are essential nutrients for plant development, leading to improved crop yields and quality.
Used in Horticultural Industry:
In horticulture, DIAMMONIUM HYDROGEN PHOSPHATE-15N2 is used as a growth promoter to support the health and vigor of ornamental plants. DIAMMONIUM HYDROGEN PHOSPHATE-15N2's nutrient profile contributes to lush foliage, vibrant blooms, and overall plant health.
Used in Research Applications:
DIAMMONIUM HYDROGEN PHOSPHATE-15N2 is utilized as a research tool for studying nitrogen cycling in ecosystems. The 15N isotopic labeling allows scientists to monitor the movement and transformation of nitrogen within plants and soil, providing insights into nutrient uptake, assimilation, and environmental impacts.
Used in Soil Analysis:
DIAMMONIUM HYDROGEN PHOSPHATE-15N2 is employed in soil analysis to assess the availability and mobility of nitrogen in the soil. This information is crucial for optimizing fertilizer applications and managing soil health for sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 287488-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,4,8 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 287488-11:
(8*2)+(7*8)+(6*7)+(5*4)+(4*8)+(3*8)+(2*1)+(1*1)=193
193 % 10 = 3
So 287488-11-3 is a valid CAS Registry Number.

287488-11-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ammonium dihydrogen phosphate-15N

1.2 Other means of identification

Product number -
Other names Ammonium-15N dihydrogen phosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:287488-11-3 SDS

287488-11-3Upstream product

287488-11-3Downstream Products

287488-11-3Relevant articles and documents

Solid phosphoric acid catalyst: A multinuclear NMR and theoretical study

Krawietz, Thomas R.,Lin, Ping,Lotterhos, Karen E.,Torres, Paul D.,Barich, Dewey H.,Clearfield, Abraham,Haw, James F.

, p. 8502 - 8511 (1998)

The synthesis, structure, and acid function of solid phosphoric acid (SPA) catalyst were studied in detail. 31P and 29Si MAS NMR and X-ray powder diffraction identified the following crystalline silicon phosphate phases in SPA: Si5O(PO4)6, hexagonal-SiP2O7, Si(HPO4)2·H2O, and SiHP3O10. The acidity of SPA is due to a liquid or glassy solution of phosphoric acid oligomers supported on the silicon phosphate phases. 15N MAS NMR of adsorbed pyridine-15N and 13C MAS NMR of adsorbed acetone-2- 13C showed Bronsted acid sites and no Lewis acid sites. 1H→15N→31P and 1H→13C→31P double cross polarization MAS NMR of the probe molecules provided a rare opportunity to use NMR to unambiguously localize chemisorption sites; the probe molecules are complexed to phosphoric acid and pyrophosphoric acid but not to the silicon phosphate phases. In situ NMR of the oligomerization of propene on SPA suggests that propene quantitatively reacts with phosphoric acid and its oligomers to form isopropyl phosphate, and formation of this very stable intermediate accounts for the lower olefin oligomerization activity of SPA relative to acidic zeolites. Theoretical calculations including geometries at B3LYP/6-311+G(d,p) and chemical shifts at GIAO-MP2/tzp/dz were used to model complexation of acetone or propene to SPA, and these support our conclusions.

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