40262
N,N-Dimethylformamide dibutyl acetal
for esterification of fatty acids, ≥98.0%
동의어(들):
1,1-Dibutoxy-N,N-dimethylmethylamine, 1,1-Dibutoxytrimethylamine
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모든 사진(2)
About This Item
Linear Formula:
(CH3)2NCH(OCH2CH2CH2CH3)2
CAS Number:
Molecular Weight:
203.32
Beilstein:
1098693
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
분석
≥98.0%
품질
for esterification of fatty acids
refractive index
n20/D 1.417
bp
93 °C/12 mmHg (lit.)
density
0.853 g/mL at 20 °C (lit.)
SMILES string
CCCCOC(OCCCC)N(C)C
InChI
1S/C11H25NO2/c1-5-7-9-13-11(12(3)4)14-10-8-6-2/h11H,5-10H2,1-4H3
InChI key
GSFFXKGTGPMVLM-UHFFFAOYSA-N
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일반 설명
N,N-Dimethylformamide dibutyl acetal (1,1-Dibutoxytrimethylamine, 1,1-Dibutoxy-N,N-dimethylmethylamine) is a dimethylformamide dialkyl acetal. Its synthesis has been reported by Meerwin and coworkers by reaction of N,N-Dimethylformamide diethyl acetal with butanol.
애플리케이션
N,N-Dimethylformamide dibutyl acetal is the suitable reagent used for the simultaneous quantification of cocaine and its primary metabolite, benzoyl ecgonine, from a urine matrix by gas-chromatography. It may be used as reagent for the esterification of fatty acids.
기타 정보
Reagent for the esterification of fatty acids; Review
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
127.4 °F - closed cup
Flash Point (°C)
53 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
J.P. Thenot et al.
Analytical Letters, 217-217 (1972)
DeWolfe RH.
Carboxylic Ortho Acid Derivatives: Preparation and Synthetic Applications (Academic press), 14, 424-424 (2012)
N C Jain et al.
Journal of forensic sciences, 22(1), 7-16 (1977-01-01)
A gas chromatographic procedure has been developed for the simultaneous determination of cocaine and benzoyl ecgonine in urine specimens. The two drugs are extracted by isopropanol/chloroform from urine samples saturated with a bisalt buffer. The organic extract is evaporated to
R.F. Abdulla et al.
Tetrahedron, 35, 1675-1675 (1979)
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