Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: BUTYRAMIDE, N-METHYL-
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Purity: 98.0%
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17794-44-4

17794-44-4 structure

Name: BUTYRAMIDE, N-METHYL-
Chemical Name: N-Methylbutanamide
CAS Number: 17794-44-4
Molecular Formula: C₅H₁₁NO
Molecular Weight: 101.14700
Create Date: 2017-06-30 08:59:12
Modify Date: 2025-10-04 13:43:54

Name	N-Methylbutanamide
Synonyms	Methyl butyric acid amide N-Methylbutyramide N-Methyl-butyramid N-methylbutyrylamide N-propyl-N-methyl-formamide BUTYRAMIDE,N-METHYL Buttersaeure-methylamid Butanamide,N-methyl

Density	0.864g/cm3
Boiling Point	210.8ºC at 760 mmHg
Molecular Formula	C₅H₁₁NO
Molecular Weight	101.14700
Flash Point	108.3ºC
Exact Mass	101.08400
PSA	29.10000
LogP	0.92340
Vapour Pressure	0.189mmHg at 25°C
Index of Refraction	1.407

CHEMICAL IDENTIFICATION

RTECS NUMBER :: ES4857500

CHEMICAL NAME :: Butyramide, N-methyl-

CAS REGISTRY NUMBER :: 17794-44-4

BEILSTEIN REFERENCE NO. :: 1740744

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C5-H11-N-O

MOLECULAR WEIGHT :: 101.17

WISWESSER LINE NOTATION :: 3VM1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Unreported

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: 2 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 18,645,1968

109480-78-6

~92%

17794-44-4

Literature: Fukuzawa, Hiroko; Ura, Yasuyuki; Kataoka, Yasutaka Journal of Organometallic Chemistry, 2011 , vol. 696, # 23 p. 3643 - 3648

141-75-3

74-89-5

~83%

17794-44-4

Literature: Beacon Laboratories, Inc. Patent: EP1216986 A2, 2002 ; Location in patent: Page 7 ;

541-35-5

1719-57-9

~82%

17794-44-4

Literature: Bassindale, Alan R.; Parker, David J.; Patel, Pravin; Taylor, Peter G. Tetrahedron Letters, 2000 , vol. 41, # 25 p. 4933 - 4936

74-89-5

107-92-6

17794-44-4

Literature: Dawson et al. Journal of the American Chemical Society, 1957 , vol. 79, p. 298

105-54-4

74-89-5

17794-44-4

Literature: Haces, Alberto; Breitman, Theodore B. R.; Driscoll, John S. Journal of Medicinal Chemistry, 1987 , vol. 30, # 2 p. 405 - 409

109-74-0

74-89-5

17794-44-4

Literature: de Benneville et al. Journal of Organic Chemistry, 1956 , vol. 21, p. 1072,1075

96-31-1

107-92-6

17794-44-4

15719-64-9

Literature: Hoshino et al. Bulletin of the Chemical Society of Japan, 1952 , vol. 25, p. 392,393

Precursor 9
109480-78-6 141-75-3 74-89-5 541-35-5
1719-57-9 107-92-6 105-54-4 109-74-0
96-31-1
DownStream 2
110-68-9 6973-82-6

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