이소낙산

이소낙산
이소낙산 구조식 이미지
카스 번호:
79-31-2
한글명:
이소낙산
동의어(한글):
아이소뷰틸산;이소낙산;이소부틸산;아이소뷰틸산;아이소부티릭애씨드
상품명:
Isobutyric acid
동의어(영문):
2-METHYLPROPIONIC ACID;Isobutanoic acid;Isobutric acid;2-METHYL PROPANOIC ACID;METHYLPROPIONIC ACID;FEMA 2222;Cenex RP b2;Tenox EBP 2;iso-C3H7COOH;i-Butyricacid
CBNumber:
CB3367722
분자식:
C4H8O2
포뮬러 무게:
88.11
MOL 파일:
79-31-2.mol
MSDS 파일:
SDS

이소낙산 속성

녹는점
-47 °C (lit.)
끓는 점
153-154 °C (lit.)
밀도
0.95 g/mL at 25 °C (lit.)
증기 밀도
3.04 (vs air)
증기압
1.5 mm Hg ( 20 °C)
굴절률
n20/D 1.393(lit.)
FEMA
2222 | ISOBUTYRIC ACID
인화점
132 °F
저장 조건
Store below +30°C.
용해도
618g/l
물리적 상태
액체
산도 계수 (pKa)
4.84(at 20℃)
색상
무색의
수소이온지수(pH)
3.96(1 mM solution);3.44(10 mM solution);2.93(100 mM solution);
냄새
프로필렌 글리콜 중 1.00%. 산성 신 치즈 낙농 버터 같은 썩은 냄새
?? ??
산성의
Odor Threshold
0.0015ppm
폭발한계
1.6-7.3%(V)
수용성
210g/L(20℃)
Merck
14,5155
JECFA Number
253
BRN
635770
Dielectric constant
2.6(Ambient)
InChIKey
KQNPFQTWMSNSAP-UHFFFAOYSA-N
LogP
1.1 at 25℃
CAS 데이터베이스
79-31-2(CAS DataBase Reference)
NIST
Propanoic acid, 2-methyl-(79-31-2)
EPA
Isobutyric acid (79-31-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn
위험 카페고리 넘버 21/22
안전지침서 23-36/37/39-24/25
유엔번호(UN No.) UN 2529 3/PG 3
WGK 독일 1
RTECS 번호 NQ4375000
F 고인화성물질 13
자연 발화 온도 824 °F
TSCA Yes
위험 등급 3
포장분류 III
HS 번호 29156000
유해 물질 데이터 79-31-2(Hazardous Substances Data)
독성 LD50 orally in Rabbit: 266 mg/kg LD50 dermal Rabbit 475 mg/kg
기존화학 물질 KE-24875
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H226 인화성 액체 및 증기 인화성 액체 구분 3 경고
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H311 피부와 접촉하면 유독함 급성 독성 물질 - 경피 구분 3 위험 GHS hazard pictograms P280, P302+P352, P312, P322, P361,P363, P405, P501
H314 피부에 심한 화상과 눈에 손상을 일으킴 피부부식성 또는 자극성물질 구분 1A, B, C 위험 GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P233 용기를 단단히 밀폐하시오. 용기는 환기가 잘 되는 곳에 단단히 밀폐하여 보관하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P303+P361+P353 피부(또는 머리카락)에 묻으면 오염된 모든 의복은 벗거나 제거하시오 피부를 물로 씻으시오/샤워하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
2
3 0

이소낙산 C화학적 특성, 용도, 생산

화학적 성질

Isobutyric acid is a clear colorless oily liquid with an odor and flavor similar to n-butyric acid. Miscible with water, soluble in ethanol and ether. Prepared via oxidation of isobutyl alcohol.

물리적 성질

Isobutyric Acid is a flavoring agent that is a colorless liquid with a strong, penetrating odor, resembling butter. it is miscible in alcohol, propylene glycol, glycerin, mineral oil, and most fixed oils and soluble in water. it is obtained by chemical synthesis. it is also termed isopropylformic acid.

출처

Isobutyric acid occurs naturally in Ceratonia siliqua L. The gum obtained from the kernels of this species is used as a thickener in the food industry. Reported found in several essential oils: Arnica montana, Roman chamomile, Laurus nobilis, imperatoria, and in carob fruits (Siliqua dulcis); also identified in the essence of Seseli tortuosum, Artemisia transiliensis.

제조 방법

Isobutyric acid is prepared in a similar way to butyric acid, mainly by direct oxidation of isobutanol and isobutyraldehyde, which is obtained by a direct oxidation reaction with air or oxygen.

정의

ChEBI: Isobutyric acid is a branched fatty acid comprising propanoic acid carrying a methyl branch at C-2. It has a role as a volatile oil component, a plant metabolite and a Daphnia magna metabolite. It is a branched-chain saturated fatty acid, a methyl-branched fatty acid and a fatty acid 4:0. It is a conjugate acid of an isobutyrate.

주요 응용

Isobutyric acid is mainly used in the synthesis of isobutyric acid esters, such as methyl isobutyrate, propyl ester, isoamyl ester and benzyl ester. It can also be used manufacture of esters for solvents, flavors and perfume bases, disinfecting agent, varnish, plasticizers, deliming hides, tanning agent and used in pharmaceutical. Isobutyric acid has some important derivatives that, in the industry, is actually used for the production of isobutyronitrile intermediates, and then converted to isobutylamidine hydrochloride that is the raw materials of pesticide diazinon.

일반 설명

Isobutyric acid appears as a colorless liquid with a light odor of rancid butter. Flash point 132°F. Density 7.9 lb / gal. Corrosive to metals and tissue.

공기와 물의 반응

Flammable. Water soluble

반응 프로필

Isobutyric acid corrodes aluminum and other metals. Flammable hydrogen gas may accumulate in enclosed spaces in which this reaction has taken place [USCG, 1999].

위험도

Toxic by ingestion, strong irritant to tissue.

건강위험

Inhalation causes irritation of nose and throat. Ingestion causes irritation of mouth and stomach. Contact with eyes or skin causes irritation.

화재위험

Flammable/combustible material. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Synthesis

The preparation of isobutyric acid is similar with butyric acid, which is performed by the direct oxidation of isobutyl alcohol and isobutyraldehyde. Isobutyric acid can be directly generated from the oxidation of isobutyraldehyde in air or oxygen. Other manufacturing methods have isobutyronitrile hydrolysis and methacrylic acid hydrogenation. The oxidation of 2-methyl-1-nitropropane to prepare isobutyric acid can also obtain a higher yield. The purification of Isobutyric acid can be realized by azeotropic distillation with water, and anhydrous isobutyric acid can be obtained by the extractive distillation from carbon tetrachloride. Propylene and formic acid ester can react at 50 °C with the catalysis of hydrofluoric acid to generate methyl isobutyrate and propyl isobutyrate.

Purification Methods

Distil the acid from KMnO4, then redistil it from P2O5. [Beilstein 2 H 288, 2 I 126, 2 II 257, 2 III 637, 2 IV 843.]

이소낙산 준비 용품 및 원자재

원자재

준비 용품


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