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MPTPHYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 39794-99-5 Structure
  • Basic information

    1. Product Name: MPTPHYDROCHLORIDE
    2. Synonyms: CYPERQUAT;Caswell no. 574c;Cyperquat chloride;Cyperquat chloride [iso];Epa pesticide chemical code 271700;Gcp-1634;S 21634
    3. CAS NO:39794-99-5
    4. Molecular Formula: C12H12N.Cl
    5. Molecular Weight: 205.687
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 39794-99-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: MPTPHYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: MPTPHYDROCHLORIDE(39794-99-5)
    11. EPA Substance Registry System: MPTPHYDROCHLORIDE(39794-99-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 39794-99-5(Hazardous Substances Data)

39794-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39794-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,9 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39794-99:
(7*3)+(6*9)+(5*7)+(4*9)+(3*4)+(2*9)+(1*9)=185
185 % 10 = 5
So 39794-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N.ClH/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11;/h2-10H,1H3;1H/q+1;/p-1

39794-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyperquat chloride

1.2 Other means of identification

Product number -
Other names CYPERQUAT CHLORIDE

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:39794-99-5 SDS

39794-99-5Downstream Products

39794-99-5Relevant articles and documents

Ultralong room-temperature phosphorescence of a solid-state supramolecule between phenylmethylpyridinium and cucurbit[6]uril

Zhang, Zhi-Yuan,Liu, Yu

, p. 7773 - 7778 (2019/08/30)

Long-lived organic room-temperature phosphorescence (RTP) has received great attention because of its various potential applications. Herein, we report a persistent RTP of a solid-state supramolecule between a cucurbit[6]uril (CB[6]) host and a heavy-atom

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides

-

, (2008/06/13)

5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides of the formula STR1 where R1 is hydrogen, a metal atom or an unsubstituted or substituted ammonium radical, R2 is a saturated or unsaturated straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical or 3 to 7 carbon atoms, a branched saturated or unsaturated aliphatic radical of 3 to 10 carbon atoms, a halogen-, alkoxy- or alkylmercapto-substituted aliphatic radical of 2 to 10 carbon atoms tetrahydrofuryl substituted methyl, a cycloalkoxy-substituted aliphatic radical of 4 to 10 carbon atoms, unsubstituted or halogen-substituted benzyl or phenyl, halophenyl, or alkylphenyl of a total of up to 10 carbon atoms, R3 is hydrogen, a straight-chain aliphatic radical of up to 10 carbon atoms, a cycloaliphatic radical of 3 to 7 carbon atoms, a branched aliphatic radical of 3 to 10 carbon atoms, haloalkyl, or alkoxyalkyl of 2 to 10 carbon atoms and X is oxygen and may also be sulfur if R2 is unsubstituted or halogen-substituted benzyl, processes for their preparation, and herbicides containing the above compounds.

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