CAS 41479-14-5 Bis(2-hydroxyethyl) terephthalate (HCID 13739)

概要

Bis(2-hydroxyethyl) terephthalate is a carboxylic ester and a diester.

名称と識別子

優先名称: Bis(2-hydroxyethyl) terephthalate
IUPAC: bis(2-hydroxyethyl) benzene-1,4-dicarboxylate
英語名: bis(2-hydroxyethyl) benzene-1,4-dicarboxylate
分子式: C12H14O6
分子量: 0

名称と別名

BIS(2-HYDROXYETHYL) TEREPHTHALATE959-26-2Bis(hydroxyethyl) terephthalateBis(beta-hydroxyethyl) terephthalateTerephthalic acid, bis(2-hydroxyethyl) ester1,4-Benzenedicarboxylic acid, bis(2-hydroxyethyl) esterBis(ethylene glycol) terephthalateJ61IL5R964DTXSID3052644RefChem:1079937DTXCID0031217213-497-6

名称をさらに表示

Glycol terephthalateTerephthalic acid, polyethylene glycol, diesterPoly(oxy-1,2-ethanediyl), alpha,alpha'-(1,4-phenylenedicarbonyl)bis(omega-hydroxy-

BHETbis(2-hydroxyethyl) benzene-1,4-dicarboxylateTerephthalic Acid Bis(2-hydroxyethyl) EsterMFCD00081066TEREPHTHALICACIDBIS(2-HYDROXYETHYL)ESTERBis(2-hydroxyethyl)terephthalate41479-14-5SCHEMBL26378

データベース識別子

CAS: 41479-14-5、959-26-2
PubChem CID: 13739
DTXSID: DTXSID3052644
ChEBI: CHEBI:231672
UNII: J61IL5R964
EC Number: 213-497-6
Nikkaji: J141.640E

物性

構造計算による物性

XLogP: 1.7
極性表面積: 93.1 Å²
水素結合供与体数: 2
水素結合受容体数: 6
回転可能結合数: 8
重原子数: 18
形式電荷: 0
複雑度: 242

実験および物理化学的性質

Chemical ClassesOther Classes -> Other Aromatic Compounds

Vapor Pressure0.00000011 [mmHg]

物理化学的性質

EPAの化学物質情報: Poly(oxy-1,2-ethanediyl), .alpha.,.alpha.'-(1,4-phenylenedicarbonyl)bis[.omega.-hydroxy- (41479-14-5)

安全と法規制

GHS分類

GHS Classification · 3 件

This chemical does not meet GHS hazard criteria for 99.1% (105 of 106) of all reports.

Not Classified

Aggregated GHS information provided per 106 reports by companies from 2 notifications to the ECHA C&L Inventory.

危険有害性情報

Regulatory Information · 4 件

Chemical: Poly(oxy-1,2-ethanediyl), .alpha.,.alpha.'-(1,4-phenylenedicarbonyl)bis[.omega.-hydroxy-

1,4-Benzenedicarboxylic acid, 1,4-bis(2-hydroxyethyl) ester is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1,4-Benzenedicarboxylic acid, 1,4-bis(2-hydroxyethyl) ester are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

FRI - indicates a polymeric substance containing no free-radical initiator in its Inventory name but is considered to cover the designated polymer made with any free-radical initiator regardless of the amount used.

Status: Active Update: 10-01-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/33876

Hazards SummaryMay cause irritation; [MSDSonline]

Hazard Classes and CategoriesNot Classified

安全と保護具

Disposal Methods · 1 件

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

毒性情報

Non-Human Toxicity Excerpts · 1 件

THE REDUCTASE ENZYME SYSTEM WHICH REDUCES P-DIMETHYLAMINOAZOBENZENE (DAB) & RELATED DYES & DEMETHYLASE ENZYME SYSTEMS WHICH N-DEMETHYLATE DAB ACTIVITIES OF LIVER FROM RATS FED THE DAB DIET WITH OR WITHOUT DISODIUM TEREPHTHALATE WERE MEASURED TO CLARIFY THE PARTICIPATION OF TEREPHTHALIC ACID IN DAB METABOLISM. BETA-HYDROXYETHYL TEREPHTHALATE INCREASED THE REDUCTASE ACTIVITY WHEN IT WAS GIVEN WITH DAB.

安全データ

tsca: TSCA listed

化学と産業

用途と製造

Uses · 2 件

Used in the production of polyethylene terephthalate; [HSDB]

CAPTIVE CHEM INT IN MFR OF POLYETHYLENE TEREPHTHALATE

U.S. Production2022: 41,000 lb

Consumption PatternsESSENTIALLY 100% AS CAPTIVE CHEM INT FOR POLYETHYLENE TEREPHTHALATE

Methods of ManufacturingTRANSESTERIFICATION OF ETHYLENE GLYCOL WITH DIMETHYL TEREPHTHALATE; ESTERIFICATION OF ETHYENE GLYCOL WITH TEREPHTHALIC ACID

General Manufacturing Information · 3 件

1,4-Benzenedicarboxylic acid, 1,4-bis(2-hydroxyethyl) ester: ACTIVE

Poly(oxy-1,2-ethanediyl), .alpha.,.alpha.'-(1,4-phenylenedicarbonyl)bis[.omega.-hydroxy-: ACTIVE

Bis(2-hydroxyethyl)terephthalate is formed as an intermediate in the manufacture of poly(ethylene terephthalate) through the esterification of terephthalic acid to form bishydroxyethyl terephthalate which is then polymerized in a transesterification reaction catalyzed by antimony oxide to form poly(ethylene terephthalate).