191529-08-5

• 

• Basic information

  1. Product Name: 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-
  2. Synonyms: 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-;[2,4,6-tribromo-3,5-bis(hydroxymethyl)phenyl]methanol
  3. CAS NO:191529-08-5
  4. Molecular Formula: C₉H₉Br₃O₃
  5. Molecular Weight: 404.87796
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 191529-08-5.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 536.2±45.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 2.256±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 12.71±0.10(Predicted)
  10. CAS DataBase Reference: 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-(191529-08-5)
  12. EPA Substance Registry System: 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-(191529-08-5)

• 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: 191529-08-5(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

191529-08-5 Suppliers

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• 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-

  Cas No: 191529-08-5

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• Enke Pharma-tech Co.,Ltd. （Cangzhou, China ）
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• 1,3,5-Benzenetrimethanol, 2,4,6-tribromo-

  Cas No: 191529-08-5

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• 191529-08-5

  Cas No: 191529-08-5

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• Nanjing Norris Pharm Technology Co., Ltd.
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191529-08-5 Usage

General Description

1,3,5-Benzenetrimethanol, 2,4,6-tribromo- is a chemical compound that is commonly used as a flame retardant and as an additive in a variety of industrial and consumer products. It is synthesized through the bromination of 1,3,5-benzenetrimethanol, resulting in a highly stable and heat-resistant compound that is effective at reducing the flammability of materials. Due to its flame-retardant properties, it is often used in the manufacturing of plastics, textiles, and electronic components, as well as in the construction and automotive industries. However, there is some concern about the potential environmental and health impacts of this chemical, including its persistence in the environment and its potential toxicity to aquatic organisms and humans. As a result, there is ongoing research and regulation aimed at minimizing the risks associated with the use of 1,3,5-Benzenetrimethanol, 2,4,6-tribromo- in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 191529-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,2 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 191529-08:
(8*1)+(7*9)+(6*1)+(5*5)+(4*2)+(3*9)+(2*0)+(1*8)=145
145 % 10 = 5
So 191529-08-5 is a valid CAS Registry Number.

191529-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	[2,4,6-tribromo-3,5-bis(hydroxymethyl)phenyl]methanol

1.2 Other means of identification

Product number	-
Other names	1,3,5-tribromo-2,4,6-trihydroxymethyl-benzene

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:191529-08-5 SDS

191529-08-5Upstream product

• 608-72-0 2,4,6-tribromomesitylene 
• 127-08-2 potassium acetate 
• 108-67-8 1,3,5-trimethyl-benzene 
• 29165-34-2 1,3,5-tris(bromo)-2,4,6-tris(bromomethyl) benzene 
• 467420-07-1 (2,4,6-tribromobenzene-1,3,5-triyl)tris(methylene) triacetate 

191529-08-5Downstream Products

• 1392224-10-0 C₁₈H₃₀O₃S₃ 
• 86216-69-5 2,4,6-tribromo-1,3,5-trisbenzoyl chloride 
• 86216-68-4 2,4,6-tribromo-1,3,5-benzene tricarboxylic acid 
• 60510-14-7 1,3,5-tribromo-2,4,6-tricyanobenzene 
• 1402134-31-9 1,3,5-tribromo-2,4,6-tri(hydroxyiminomethyl)benzene 
• 191529-13-2 1,3,5-Tris-(2,2-dibromo-vinyl)-2,4,6-tris-triethylsilanylethynyl-benzene 
• 191529-12-1 1,3,5-Tris-(2,2-dibromo-vinyl)-2,4,6-tris-phenylethynyl-benzene 
• 191529-11-0 2,4,6-Tris-triethylsilanylethynyl-benzene-1,3,5-tricarbaldehyde 
• 191529-10-9 2,4,6-tris(phenylethynyl)benzene-1,3,5-tricarbaldehyde 
• 502157-79-1 1,3,5-tris(2,2-dibromo-1-ethenyl)-2,4,6-tris[(trimethylsilyl)ethynyl]benzene 
• 502157-78-0 2,4,6-tris[(trimethylsilyl)ethynyl]-1,3,5-benzenetricarbaldehyde 
• 191529-09-6 2,4,6-tribromo-1,3,5-benzenetricarboxaldehyde 

191529-08-5Relevant articles and documents

Interfacial synthesis of crystalline two-dimensional cyano-graphdiyne

Chen, Siqi,Li, Zhibo,Pan, Qingyan,Shao, Feng,Sun, Qingzhu,Wu, Chenyu,Zhang, Zhaohui,Zhao, Yingjie

, p. 3210 - 3213 (2020/03/23)

A well-defined crystalline cyano-functionalized graphdiyne (CN-GDY) is synthesized at a liquid/liquid interface through alkyne-alkyne coupling reactions. The configurations and nanostructures of CN-GDY were well characterized by TEM, SEM, AFM, XPS, and Raman spectroscopy. HR-TEM and selected area electron diffraction (SAED) in combination with structure simulation firmly revealed a 9-fold stacking mode for CN-GDY.

Organic light-emitting diode materials

-

Paragraph 0395; 0396, (2017/07/26)

Described herein are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moiety D, each moiety D is covalently attached to either the moiety B or the moiety A, and each moiety B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D, and B are defined herein.

En route to archimedene: Total synthesis of C3h-symmetric [7]phenylene

Bruns, Dirk,Miura, Hirokazu,Vollhardt, K. Peter C.,Stanger, Amnon

, p. 549 - 552 (2007/10/03)

(Matrix presented) The total synthesis of C3h-symmetric [7]phenylene has been accomplished by triple cobalt-catalyzed cycloisomerization of an appropriate nonayne. Its spectral data are in accord with the expectations for a triply angularly fus

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