W359904
trans-2-Methyl-2-butenoic acid
≥99%, FG
동의어(들):
Tiglic acid, trans-2,3-Dimethylacrylic acid, trans-2-Methyl-2-butenoic acid
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
CH3CH=C(CH3)COOH
CAS Number:
Molecular Weight:
100.12
FEMA Number:
3599
Beilstein:
1236500
EC Number:
유럽평의회 번호:
10168
MDL number:
UNSPSC 코드:
12164502
PubChem Substance ID:
플래비스(Flavis) 번호:
8.064
NACRES:
NA.21
추천 제품
생물학적 소스
synthetic
Grade
FG
Fragrance grade
Halal
Kosher
Agency
follows IFRA guidelines
meets purity specifications of JECFA
규정 준수
EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
분석
≥99%
bp
95-96 °C/12 mmHg (lit.)
mp
61-64 °C (lit.)
density
0.969 g/mL at 25 °C (lit.)
응용 분야
flavors and fragrances
문건
see Safety & Documentation for available documents
식품 알레르기항원
no known allergens
향수 알레르기항원
no known allergens
감각 수용성의
brown; spicy
SMILES string
C\C=C(/C)C(O)=O
InChI
1S/C5H8O2/c1-3-4(2)5(6)7/h3H,1-2H3,(H,6,7)/b4-3+
InChI key
UIERETOOQGIECD-ONEGZZNKSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
- A high molar extinction coefficient bisterpyridyl homoleptic Ru(II) complex with trans-2-methyl-2-butenoic acid functionality: potential dye for dye-sensitized solar cells.: This study explores the synthesis and application of a Ru(II) complex incorporating trans-2-methyl-2-butenoic acid as a dye for dye-sensitized solar cells. The high molar extinction coefficient and favorable photophysical properties make this compound a promising candidate for enhancing solar cell efficiency (Adeloye et al., 2012).
- Synthesis, photophysical and electrochemical properties of a mixed bipyridyl-phenanthrolyl ligand Ru(II) heteroleptic complex having trans-2-methyl-2-butenoic acid functionalities.: This research focuses on the synthesis and characterization of a Ru(II) heteroleptic complex with trans-2-methyl-2-butenoic acid functionalities. The study highlights the compound′s photophysical and electrochemical properties, demonstrating its potential for use in optoelectronic devices and catalytic applications (Adeloye, 2011).
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
203.0 °F
Flash Point (°C)
95 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Susan Matthew et al.
Phytochemistry, 70(17-18), 2058-2063 (2009-10-10)
The Floridian marine cyanobacterium Lyngbya confervoides afforded cyclodepsipeptides, termed tiglicamides A-C (1-3), along with their previously reported analogues largamides A-C (4-6), all of which possess an unusual tiglic acid moiety. Their structures were deduced by one- and two-dimensional NMR combined
Shao-Liang Zheng et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(2), 706-713 (2007-10-24)
[Zn(TA)2(H2O)2] (H-TA=tiglic acid) has been embedded in a framework composed of CECR (CECR=C-ethylcalix[4]resorcinarene) molecules to examine its E-->Z photoisomerization in a periodic framework. The photoisomerization of tiglic acid in CECR-[Zn(TA)2(H2O)2]4 H2O proceeds without the [2+2]-dimerization reaction that often occurs in
Inhibition of mitochondrial creatine kinase activity from rat cerebral cortex by methylmalonic acid.
P F Schuck et al.
Neurochemistry international, 45(5), 661-667 (2004-07-06)
Accumulation of methylmalonic acid (MMA) in tissues and biological fluids is the biochemical hallmark of patients affected by the neurometabolic disorder known as methylmalonic acidemia (MMAemia). Although this disease is predominantly characterized by severe neurological findings, the underlying mechanisms of
R H Lindecrona et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 41(5), 647-654 (2003-03-28)
Groups of 10 male and 10 female rats were administered 0, 25, 100 or 400 mg octan-3-ol/kg body weight per day, 77 mg 2-methylcrotonic acid/kg body weight per day or 163 mg oct-3-yl 2-methylcrotonate/kg body weight per day by gavage
Mian Zhang et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 40(6), 529-532 (2005-09-08)
To study the chemical constituents of the underground part of Ligularia pleurocaulis (Franch.) Hand-Mazz. The dried roots and rhizomes of L. pleurocaulis were extracted with methanol. Isolation and purification were performed by silica gel column chromatography and recrystallization etc. Structures
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