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Merck
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주요 문서

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B3000

Sigma-Aldrich

1,4-Benzenedimethanol

99%

동의어(들):

p-Phenylene dicarbinol, p-Phenylenedimethanol, p-Xylene-α,α′-diol, p-Xylylene dialcohol, NSC 5097

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모든 사진(2)

About This Item

Linear Formula:
C6H4(CH2OH)2
CAS Number:
589-29-7
Molecular Weight:
138.16
Beilstein:
2042077
EC Number:
209-641-2
MDL number:
MFCD00004665
UNSPSC 코드:
12352100
PubChem Substance ID:
24891677
NACRES:
NA.22

분석

99%

양식

powder

bp

138-143 °C/1 mmHg (lit.)

mp

114-118 °C (lit.)

SMILES string

OCc1ccc(CO)cc1

InChI

1S/C8H10O2/c9-5-7-1-2-8(6-10)4-3-7/h1-4,9-10H,5-6H2

InChI key

BWVAOONFBYYRHY-UHFFFAOYSA-N

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관련 카테고리

일반 설명

1,4-Benzenedimethanol acts as a chain extender to prepare dimethylsiloxane-urea-urethane copolymers.

애플리케이션

1,4-Benzenedimethanol can be used to prepare:
  • Poly(6-methyl-ε-caprolactone), which is a key intermediate for the synthesis of polylactide based thermoplastic elastomers.
  • A Highly cross-linked polymer named HCP−BDM (hyper cross-linked polymer-1,4-benzenedimethanol) via Friedel−Crafts alkylation in the presence of Lewis acid.
  • Sulfonated polynuclear aromatic resins.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
05031TH
03722PN
00221JF
00112EV
04609KV

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Synthesis of the sulfonated condensed polynuclear aromatic (S-COPNA) resins as strong protonic acids
Tanemura K, et al.
Tetrahedron, 67(6), 1314-1319 (2011)
Microporous organic polymers synthesized by self-condensation of aromatic hydroxymethyl monomers
Luo Y, et al.
Polym. Chem., 4(4), 1126-1131 (2013)
Polylactide-poly (6-methyl-ε-caprolactone)-polylactide thermoplastic elastomers
Martello MT and Hillmyer M A
Macromolecules, 44(21), 8537-8545 (2011)
Tiejun Ge et al.
Polymers, 11(8) (2019-08-03)
In this experiment, terephthalyl alcohol was used as a modifier to modify phenol under both acidic and alkaline conditions to obtain modified phenols with different molecular structures. Subsequently, the modified phenols reacted with paraformaldehyde in an alkaline environment. After foaming
Takumi Ishida et al.
International journal of molecular sciences, 21(7) (2020-04-05)
To investigate organic field-effect transistor (OFET) properties, a new thienoacene-type molecule, 4,14-dihexyldinaphtho[2,3-d:2',3'-d']anthra[1,2-b:5,6-b']dithiophene (C6-DNADT), consisting of π-conjugated nine aromatic rings and two hexyl chains along the longitudinal molecular axis has been successfully synthesized by sequential reactions, including Negishi coupling, epoxidation, and
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