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Merck
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Key Documents

55397

Supelco

(R)-3-Hydroxybutyric acid

analytical standard

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About This Item

실험식(Hill 표기법):
C4H8O3
CAS Number:
Molecular Weight:
104.10
Beilstein:
1720568
EC Number:
MDL number:
UNSPSC 코드:
41116107

Grade

analytical standard

분석

≥97.0% (GC)

유통기한

limited shelf life, expiry date on the label

mp

49-50 °C (lit.)

응용 분야

clinical testing

형식

neat

저장 온도

2-8°C

SMILES string

C[C@@H](O)CC(O)=O

InChI

1S/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/t3-/m1/s1

InChI key

WHBMMWSBFZVSSR-GSVOUGTGSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

(R)-3-Hydroxybutyric acid, a monomer of the polymer polyhydroxybutyrate (PHB), is widely used as a nutrition source and a precursor for vitamins, antibiotics and pheromones. Its potential as a protective agent against neuronal death is investigated.

애플리케이션

2(R)-3-Hydroxybutyric acid may be used as an analytical reference standard for the quantification of the analyte in urine samples using achiral dual-capillary column gas chromatography. It may also be used as a standard in the production of enantiopure (R)-3-HB using non-conventional yeast A. adeninivorans as a production host and glucose as a carbon source. The purity is determined using gas chromatography-mass spectrometric analysis (GC-MS).

추천 제품

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

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문서 라이브러리 방문

K R Ki et al.
Journal of chromatography. A, 891(2), 257-266 (2000-10-24)
The simultaneous enantiomeric separation of 30 racemic acids including 24 hydroxy acids in a single analysis is described for the determination of their absolute configurations. It involves the conversion of each enantiomer into diastereomeric O-trifluoroacetylated (-)-menthyl ester for the direct

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