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Merck
모든 사진(1)

주요 문서

W359904

Sigma-Aldrich

trans-2-Methyl-2-butenoic acid

≥99%, FG

동의어(들):

Tiglic acid, trans-2,3-Dimethylacrylic acid, trans-2-Methyl-2-butenoic acid

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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
감각 수용성의:
brown; spicy
Grade:
FG
Fragrance grade
Halal
Kosher
생물학적 소스:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
식품 알레르기항원:
no known allergens

생물학적 소스

synthetic

Quality Level

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).

픽토그램

Exclamation mark

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


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이미 열람한 고객

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Athula B Attygalle et al.
Journal of chemical ecology, 30(3), 577-588 (2004-05-14)
Analyses of pygidial gland contents of two species of a previously uninvestigated family of beetles (Trachypachidae) by Gas Chromatography-Mass Spectrometry (GC-MS) revealed that their chemistry is similar to that reported from many members of the family Carabidae. Nevertheless, the composition
Y S Li et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 26(12), 835-837 (2003-06-05)
To study the chemical constituents of Ligularia vellerea. The compounds were isolated by column chromatography, and the structures were identified by NMR spectral data and other methods. Seven compounds were isolated and identified as 4-hydroxyacetophenone, 8 alpha-hydroxy-7(11)-eremophilen-12, 8 beta-olide, umbelliferone
[Effects of a skin stimulating salve].
W RIESE
Wiener medizinische Wochenschrift (1946), 100(45-46), 758-759 (1950-11-25)
Araceli Larios et al.
Applied microbiology and biotechnology, 65(4), 373-376 (2004-07-13)
Candida antarctica lipase fraction B (CAL-B) showed substrate specificity in the synthesis of esters in hexane involving reactions of short-chain acids having linear (acetic and butyric acids) and branched chain (isovaleric acid) structures, an unsaturated (tiglic acid) fatty acid, and
Tigliane-type diterpene esters from Synadenium grantii.
R Bagavathi et al.
Planta medica, 54(6), 506-510 (1988-12-01)

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