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2,5-Furandicarboxylic acid

HCID 76720
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
3238-40-2
표준 SMILES
O=C(O)c1ccc(C(=O)O)o1
InChIKey
CHTHALBTIRVDBM-UHFFFAOYSA-N
분자식
C6H4O5
평균 분자량
156.093 g/mol
단동위원소 질량
156.00587323

이름 및 식별자

우선 이름
2,5-Furandicarboxylic acid
IUPAC
Furan-2,5-dicarboxylic acid
영어명
2,5-Furandicarboxylic acid
분자식
C6H4O5
분자량
156.09

이름 및 동의어

FDCAFURAN-2,5-DICARBOXYLIC ACID2,5-furandicarboxylate2,3-furandicarboxylic acid2,5-Furandicarboxylic2,5-Furandicarboxylic acid (FDCA)NSC 407405-Furandic5-FurandicarDEHYDROMUCIC ACID

데이터베이스 식별자

CAS
3238-40-2
PubChem CID
76720
DTXSID
DTXSID0062927
ChEBI
CHEBI:84212
UNII
73C4JJ695C
EC Number
221-800-8
Nikkaji
J7.694E

물성

물리화학적 성질

녹는점
300 °C · >300 °C
끓는 점
240.29 °C · 240.29°C (rough estimate)
밀도
1.74 · 1.7400
굴절률
1.64 · 1.6400 (estimate)
저장 조건
Keep in dark place,Sealed in dry,Room Temperature
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨 초음파 처리)
물리적 상태
고체
산도 계수 (pKa)
2.28 · 2.28±0.10(Predicted)
색상
흰색에서 진한 갈색까지
수용성
1 g/L · 1g/L(18ºC)
안정성
감광성, 흡습성이 매우 높음
InChI
1S/C6H4O5/c7-5(8)3-1-2-4(11-3)6(9)10/h1-2H,(H,7,8)(H,9,10)
InChIKey
CHTHALBTIRVDBM-UHFFFAOYSA-N
SMILES
OC(=O)c1ccc(o1)C(O)=O
LogP
-1.43 at · -1.43 at 20℃
NIST
-2 · Furan-2,5-dicarboxylic acid(3238-40-2)
EPA
2 · 2,5-Furandicarboxylic acid (3238-40-2)
화학적 성질 · 1건

2,5-Furandicarboxylic acid is a chemical intermediate with high sensitivity and good stability. It is soluble in water under alkaline conditions and is a white powder solid under acidic conditions, and is an important monomer for the preparation of corrosion-resistant plastics. It is irritating to eyes, respiratory tract and skin.

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
1
tsca
TSCA listed
HS 번호
29321900
risk_code
36/37/38-36
hazard_code
Xi
safety_code
26-36/37/39-36/37
위험 등급
IRRITANT
Hazard Classifications
Eye Irrit. 2
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 3건

개요2,5-Furandicarboxylic acid (FDCA) is an organic chemical compound consisting of two carboxylic acid groups attached to a central furan ring. It was first reported as dehydromucic acid by Rudolph Fittig and Heinzelmann in 1876, who produced it via the action of concentrated hydrobromic acid upon mucic acid. It can be produced from certain carbohydrates and as such is a renewable resource, it was identified by the US Department of Energy as one of 12 priority chemicals for establishing the “green” chemistry industry of the future.Furan-2,5-dicarboxylic acid (FDCA) has been suggested as an important renewable building block because it can substitute for terephthalic acid (PTA) in the production of polyesters and other current polymers containing an aromatic moiety.wikipedia

역사2,5-Furandicarboxylic acid, also known as dehydromucic acid, is a furan derivative. This organic compound was first obtained by Fittig and Heinzelmann in 1876. More than 125 years later, FDCA was identified by the US Department of Energy as one of 12 priority chemicals for establishing the "green" chemistry industry of the future. On a laboratory scale, it is often synthesized from 5- hydroxymethylfurfural (HMF), which in turn can be obtained from carbohydrate-containing sources such as glucose, fructose, sucrose, and starch. From fructose and glucose, HMF is obtained by acidic eliminating three moles of water.

용도Interest in renewable based polymers has led to 2,5-furandicarboxylic acid being proposed as a green, sustainable alternative to the widely used petroleum-based terephthalic acid in the synthesis of polyesters. 2,5-Furandicarboxylic acid is produced from oxidation of 5-hydroxymethylfurfural (HMF) which is obtained from the dehydration of bio-based sugars such as fructose.

제조 방법 · 1건

2,5-Furandicarboxylic acid (FDCA) can be produced from biomass or its derived sugars or platform chemicals, and has demonstrated to be a very promising substitute for petroleum-derived polymer products.Chapter 5 - Advances in the synthesis and application of 2,5-furandicarboxylic acid

상·하류 제품 정보

상류 원료

5-하이드록시메틸-2-푸르알데하이드

관련 반응

6건
반응 기록 만들기
HRID 1385756 반응식
HRID 1385756반응물로uspto-grants-2001_07
HRID 1424747 반응식
HRID 1424747반응물로uspto-grants-2015_01
HRID 1583179 반응식
HRID 1583179반응물로uspto-grants-2004_05
HRID 1636139 반응식
HRID 1636139반응물로uspto-grants-2003_01
HRID 1871750 반응식
HRID 1871750반응물로uspto-grants-2000_08
HRID 1889211 반응식
HRID 1889211반응물로uspto-grants-2013_08

화합물 노트

불러오는 중…

이 페이지에서기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
염산
질산
과망간산칼륨
수산화나트륨
L-erythro-5-Hexulosuronic acid, 4-deoxy-
5-(ethoxycarbonyl)furan-2-carboxylic acid
2,5-푸란디카복실산디에틸에스테르
에틸알코올

하류 제품

8-OXA-3-AZABICYCLO[3.2.1]옥탄수소염5-하이드록시메틸-푸란-2-카르복실산5-니트로-2-푸로산2,5-Furandicarboxylic acid, 2,5-dihydro-, cis-

공급사100 곳

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추가 설명

정의ChEBI: A member of the class of furans carrying two carboxy substituents at positions 2 and 5.