10556-98-6

• 

• Basic information

  1. Product Name: 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE
  2. Synonyms: 1,3,5-Triisopropyl-1,3,5-triazinane;Hexahydro-1,3,5-triisopropyl-s-triazine;s-Triazine, hexahydro-1,3,5-triisopropyl-;1,3,5-TRIISOPROPYLHEXAHYDRO-1,3,5-TRIAZINE;1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE;1,3,5-Tiisopropylhexahydro-1,3,5-triazine;1,3,5-Triazine, hexahydro-1,3,5-tris(1-methylethyl)-;1,3,5-TRIISOPROPYLHEXAHYDRO-1,3,5-TRIAZINE 97+%
  3. CAS NO:10556-98-6
  4. Molecular Formula: C₁₂H₂₇N₃
  5. Molecular Weight: 213.36
  6. EINECS: 234-142-1
  7. Product Categories: N/A
  8. Mol File: 10556-98-6.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 250℃
  3. Flash Point: 95℃
  4. Appearance: /
  5. Density: 0.904
  6. Vapor Pressure: 0.0228mmHg at 25°C
  7. Refractive Index: 1.472
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE(10556-98-6)
  12. EPA Substance Registry System: 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE(10556-98-6)

• 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: 10556-98-6(Hazardous Substances Data)

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• 1,3,5-Triisopropylhexahydro-1,3,5-triazine

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• USD $ 3.0-3.0 / Kilogram

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• Pharmaceutical Grade CAS 10556-98-6 with competitive price

  Cas No: 10556-98-6

• USD $ 139.0-210.0 / Kilogram

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• 1,3,5-Triazine,hexahydro-1,3,5-tris(1-methylethyl)-

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• 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE

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• 2.,3,5-TRIISOPROPYL HEXAHYDRO-SYM- TRIAZINE

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10556-98-6 Usage

General Description

1,3,5-TRIISOPROPYL HEXAHYDRO-SYM-TRIAZINE is a chemical compound belonging to the class of triazine derivatives. It is a symmetrical hexahydro-1,3,5-triisopropyl-s-triazine that is used as a corrosion inhibitor in various industrial applications, particularly in the oil and gas industry. It functions by forming a protective film on metal surfaces, preventing the formation of rust and corrosion. Additionally, it is also used as a stabilizer in polymers and as an intermediate in the synthesis of other chemicals. The compound is known for its high thermal stability, making it suitable for use in high-temperature environments. Overall, 1,3,5-TRIISOPROPYL HEXAHYDRO-SYM-TRIAZINE plays a crucial role in protecting metal equipment and components from corrosion and extending their service life.

Check Digit Verification of cas no

The CAS Registry Mumber 10556-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10556-98:
(7*1)+(6*0)+(5*5)+(4*5)+(3*6)+(2*9)+(1*8)=96
96 % 10 = 6
So 10556-98-6 is a valid CAS Registry Number.

InChI:InChI=1/C12H27N3/c1-10(2)13-7-14(11(3)4)9-15(8-13)12(5)6/h10-12H,7-9H2,1-6H3

10556-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,3,5-tri(propan-2-yl)-1,3,5-triazinane

1.2 Other means of identification

Product number	-
Other names	1,3,5-Triazine,hexahydro-1,3,5-tris(1-methylethyl)

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:10556-98-6 SDS

10556-98-6Upstream product

• 50-00-0 formaldehyd 
• 75-31-0 isopropylamine 
• 77037-04-8 N-methylideneisopropylamine 
• 75-09-2 dichloromethane 

10556-98-6Downstream Products

• 16217-22-4 3-isopropylaminopropionic acid ethyl ester 
• 86236-76-2 ethyl 1,3-diisopropylhexahydropyrimidine-5-carboxylate 
• 6056-52-6 isopropylimino-bis(methylenephosphonic acid) 
• 77891-54-4 N-isopropylaminomethylphosphonic acid 
• 996-35-0 N,N-dimethylisopropyl amine 
• 4747-21-1 N-methylpropan-2-amine 
• 86000-10-4 benzyl 3-isopropylaminopropionate 
• 79194-83-5 N-Isopropyl-N-(2-oxo-cyclohexylmethyl)-acetamide 
• 249735-52-2 3,5-dimethyl-1-isopropyl-1,3,5-triazine 
• 183617-31-4 Cu(P(C₆H₅)3)(C₃H₆N₃(C₃H₇)3)⁽¹⁺⁾*BF₄^(1-) = [Cu(P(C₆H₅)3)(C₃H₆N₃(C₃H₇)3)]BF₄ 
• 863485-14-7 4-(4-fluorophenyl)-1-isopropyl-5-methyl-1H-imidazole 3-oxide 
• 25508-61-6 p-Tolyl-isopropylaminomethyl-sulfid 
• 782387-36-4 3-isopropyl-7-methyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-ol 

10556-98-6Relevant articles and documents

Notiz zur Darstellung des N-Methylisopropylamins

Al Shaik, Mohammed,Oelschlaeger, Herbert,Rothley, Dietrich

, p. 644 - 646 (1981)

-

-

Dickinson,Graymore

, p. 1368 (1937)

-

Synthesis and Crystal Structure of Dipotassium Salts of N-Alkyl-N-{[O-alkoxy(hydroxy)phosphoryl]methyl}ditiocarbamic Acids

Garifzyanov, A. R.,Islamov, D. R.,Mirzayanov, I. I.,Shtyrlin, V. G.

, p. 381 - 384 (2020/04/27)

Abstract: A one-pot method for the synthesis of dipotassium salts of N-alkyl-N-{[O-alkoxy(hydroxy)phosphoryl]methyl}dithiocarbamic acids has been elaborated. Dipotassium salts of N-isopropyl-, N-butyl-, and N-cyclohexyl-N-{[hydroxy(O-ethoxy)phosphoryl]methyl}dithiocarbamic acids as well as N-{[O-butoxy(hydroxy)phosphoryl]methyl}-N-(2-methoxyethyl)dithiocarbamic acid have been synthesized and isolated. Crystal and molecular structure of the latter compound have been elucidated.

Facile Access to 3-Unsubstituted Tetrahydroisoquinolonic Acids via the Castagnoli-Cushman Reaction

Guranova, Natalia,Dar'In, Dmitry,Krasavin, Mikhail

, p. 2001 - 2008 (2018/03/06)

Hitherto undescribed 3-unsubstituted tetrahydroisoquinolonic acids (isolated as their respective methyl esters) were accessed for the first time by the uncatalyzed, thermally promoted Castagnoli-Cushman reaction (CCR) of homophthalic anhydride (HPA) and a series of 1,3,5-triazinanes. The moderate yields observed in some cases are most likely associated with a persistent impurity also formed in these reactions. The new scaffold is expected to find novel medicinal utility (compared to the traditional CCR adducts) because it lacks a substituent at the 3-position.

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