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1473-63-8

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1473-63-8 Usage

Chemical compound

Allylphosphonic acid dipropyl ester

Primary use

Plasticizer or stabilizer in industrial applications

Physical properties

Clear, colorless liquid with a faint odor, highly flammable

Classification

Phosphonic acid ester, organophosphorus compound

Common uses

Improves flexibility and durability of plastics, rubbers, and polymers; manufacturing of adhesives, sealants, and coatings

Safety precautions

Harmful if ingested, inhaled, or comes into contact with skin or eyes; proper safety measures should be taken when handling the chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1473-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1473-63:
(6*1)+(5*4)+(4*7)+(3*3)+(2*6)+(1*3)=78
78 % 10 = 8
So 1473-63-8 is a valid CAS Registry Number.

1473-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Di-n-propyl allylphosphonate

1.2 Other means of identification

Product number -
Other names Allylphosphonsaeure-dipropylester

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:1473-63-8 SDS

1473-63-8Relevant articles and documents

Preparation method of battery electrolyte additive

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Paragraph 0050-0051, (2021/05/08)

The invention provides a preparation method of alkenyl phosphate. The preparation method is characterized by comprising the following steps: under the protection of inert gas, adding alkenyl-containing alcohol, an imidazolium salt catalyst, a first solvent and an acid-binding agent into a reaction container, uniformly stirring, dropwise adding a halogenated phosphate solution dissolved in a second solvent into the reaction container at 0-50 DEG C, reacting for 0.5-2h, after the reaction is finished, returning to the room temperature, filtering, removing solid salt, washing the salt for 3-5 times, collecting a washing solution, adding a saturated sodium bicarbonate solution into the filtrate, stirring for 5-10 minutes, standing for liquid separation, collecting an organic phase, extracting a water phase for 3-5 times, collecting an extracting solution, combining the washing solution, the organic phase and the extracting solution, drying with anhydrous magnesium sulfate, and decolorizing with activated carbon, and rectifying under reduced pressure to obtain the product alkenyl phosphate. The imidazolium salt ionic liquid is used for preparing the alkenyl phosphate, compared with the prior art, the reaction conditions are milder, the reaction time is shorter, and very high yield and purity can be achieved.

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