말톨

말톨
말톨 구조식 이미지
카스 번호:
118-71-8
한글명:
말톨
동의어(한글):
3-히드록시-2-메틸-4-피론;말톨
상품명:
3-Hydroxy-2-methyl-4H-pyran-4-one
동의어(영문):
MALTOL;3-HYDROXY-2-METHYL-4-PYRONE;LARIXINIC ACID;3-HYDROXY-2-METHYL-4-PYRANONE;4H-Pyran-4-one, 3-hydroxy-2-methyl-;Veltol;Maltol (4 g);Vetol;Maltol ,98%;Methyl maltol
CBNumber:
CB5768714
분자식:
C6H6O3
포뮬러 무게:
126.11
MOL 파일:
118-71-8.mol
MSDS 파일:
SDS

말톨 속성

녹는점
160-164 °C(lit.)
끓는 점
205 °C
밀도
1.046 g/mL at 25 °C
증기압
0.15Pa at 24℃
굴절률
n20/D 1.541
FEMA
2656 | MALTOL
인화점
198 °F
저장 조건
2-8°C
용해도
메탄올: 50mg/mL, 투명
산도 계수 (pKa)
8.41±0.10(Predicted)
물리적 상태
액체
색상
무색의
수소이온지수(pH)
5.3 (0.5g/l, H2O)
냄새
벤질알코올 중 5.00%. 달콤한 카라멜 솜사탕 잼 과일 구운 빵
?? ??
캐러멜 같은
폭발한계
25%
수용성
1.2g/100mL(25℃)
Merck
14,5713
JECFA Number
1480
BRN
112169
InChIKey
XPCTZQVDEJYUGT-UHFFFAOYSA-N
LogP
2.3 at 25℃
CAS 데이터베이스
118-71-8(CAS DataBase Reference)
NIST
3-Hydroxy-2-methyl-4h-pyran-4-one(118-71-8)
EPA
Maltol (118-71-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi
위험 카페고리 넘버 22-38-36/37/38-41-20/22
안전지침서 37-37/39-26-36-36/37/39-36/37
유엔번호(UN No.) UN 3334
WGK 독일 3
RTECS 번호 UQ1050000
자연 발화 온도 1364 °F
위험 참고 사항 Irritant
TSCA Yes
HS 번호 29329995
유해 물질 데이터 118-71-8(Hazardous Substances Data)
기존화학 물질 KE-20692
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
1
2 0

말톨 MSDS


3-Hydroxy-2-methyl-4H-pyran-4-one

말톨 C화학적 특성, 용도, 생산

순도시험

  (1) 융점 : 이 품목의 융점은 160~164℃이어야 한다.

  (2) 용상 : 이 품목 0.1g을 70% 에탄올 5mL에 녹일 때, 그 액은 징명하여야 한다.

  (3) 비소 : 이 품목을 비소시험법에 따라 시험할 때, 그 양은 4.0ppm 이하이어야 한다.

  (4) 납 : 이 품목 5.0g을 취하여 원자흡광광도법 또는 유도결합플라즈마발광광도법에 따라 시험할 때, 그 양은 2.0ppm 이하이어야 한다.

확인시험

  (1) 이 품목 0.1g을 에탄올 10mL에 녹인 다음 염화제이철시액 3방울을 넣으면 적자색을 나타낸다.

  (2) 이 품목 0.5g에 수산화나트륨시액 10mL를 넣어 흔들어 섞으면 투명하게 녹는다. 여기에 이산화탄소를 통하면 백색 결정이 생긴다. 이 결정을 취해 50% 에탄올을 용매로 하여 재결정할 때, 그 융점은 160~163℃이다.

  (3) 이 품목 0.1g을 디옥산 5mL에 녹인 다음 수산화나트륨시액 1mL를 넣어 요오드‧요오드칼륨시액을 흔들어 섞으면서 요오드색이 없어지지 않을 때까지 넣은 후 온탕 중에서 5분간 가열하면 황색의 결정이 생긴다.

정량법

  이 품목 약 50mg을 정밀히 달아 0.1N 염산에 녹여 250mL로 한 다음 5mL를 취하여 0.1N 염산을 넣어 100mL로 하고 이를 시험용액으로 한다. 따로 말톨표준품을 사용하여 검체의 경우와 같이 처리하여 표준용액을 만들어 0.1N 염산을 대조액으로 하여 파장 274nm에서 시험용액의 흡광도 Au 및 표준용액의 흡광도 As를 측정하여 다음 계산식에 따라 말톨의 함량(%)을 구한다.

          C : 표준용액 중 말톨의 농도(μg/mL)

강열잔류물

  이 품목의 강열잔류물은 0.2% 이하이어야 한다.

개요

Maltol has a warm, sweet, fruity odor and a jam-like odor in solution. It may be prepared by alkaline hydrolysis of streptomycin salts; also from piperidine to pyromeconic acid and subsequent methylation at the 2 position.

화학적 성질

White, crystalline powder; characteristic caramel-butterscotch odor and suggestive of a fruity-strawberry aroma in dilute solution. Melting range 160–164C. Slightly soluble in water; more soluble in alcohol and propylene glycol.

출처

Reported found in the bark of young larch trees (Pinus larix), pine needles (Abies alba), chicory, wood tars and oils, and roasted malt. Also reported found in wheat and rye bread, milk, butter, smoked pork, beer, cocoa, coffee, roasted barley, filberts, peanuts, soybean, beans, tamarind, licorice, sake, malt, dried bonito, clam and cocoa liquor.

용도

A fragrance molecule used in flavor enhancers and fragrances.

생산 방법

Maltol is mainly isolated from naturally occurring sources such as beechwood and other wood tars; pine needles; chicory; and the bark of young larch trees. It may also be synthesized by the alkaline hydrolysis of streptomycin salts or by a number of other synthetic methods.

제조 방법

Maltol may be produced synthetically starting from kojic acid . Alternatively, it can be isolated from beechwood tar or from extracts of needles from the genus Abies. Commercially available extracts fromAbies balsamea needles, which are also used as flavor and fragrance materials, usually contain 3–8% maltol. It is used in aroma compositions with a caramel note and as a taste intensifier in, for example, fruit flavors (particularly in strawberry flavor compositions).

정의

ChEBI: A natural product found in Cordyceps sinensis.

일반 설명

White crystalline powder with a fragrant caramel-butterscotch odor. pH (5% aqueous solution) 5.3.

공기와 물의 반응

May be sensitive to prolonged exposure to light and air. Somewhat soluble in water at room temperature. Freely soluble in hot water [Merck]. Slightly soluble in cold water.

반응 프로필

3-Hydroxy-2-methyl-4H-pyran-4-one is weakly acidic. Reacts with bases. May react with reducing agents. Volatile with steam.

화재위험

Flash point data on 3-Hydroxy-2-methyl-4H-pyran-4-one are not available; however, 3-Hydroxy-2-methyl-4H-pyran-4-one is probably combustible.

Pharmaceutical Applications

Maltol is used in pharmaceutical formulations and food products as a flavoring agent or flavor enhancer. In foods, it is used at concentrations up to 30 ppm, particularly with fruit flavorings, although it is also used to impart a freshly baked odor and flavor to bread and cakes. When used at concentrations of 5–75 ppm, maltol potentiates the sweetness of a food product, permitting a reduction in sugar content of up to 15% while maintaining the same level of sweetness. Maltol is also used at low levels in perfumery.

Pharmacology

In mice, spontaneous motor activity was depressed by sc injection oi relatively low doses of maltol (75 mg/kg), hexobarbitone sleeping time was prolonged by sc or oral administration of 300 mg/kg, and convulsions induced by pentylenetetrazole or strychnine were inhibited by sc injection of toxic doses (500 mg/kg), but 1 mM concentrations of maltol had no effect on oxygen uptake by slices of the brain cortex of the rat (Aoyagi et al. 1974).

Safety Profile

Moderately toxic by ingestion, intraperitoneal, and subcutaneous routes. A skin irritant. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Safety

Maltol is generally regarded as an essentially nontoxic and nonirritant material. In animal feeding studies, it has been shown to be well tolerated with no adverse toxic, reproductive, or embryogenic effects observed in rats and dogs fed daily intakes of up to 200mg/kg body-weight of maltol, for 2 years.The WHO has set an acceptable daily intake for maltol at up to 1mg/kg body-weight.A case of allergic contact dermatitis, attributed to the use of maltol in a lip ointment, has been reported.
LD50 (chicken, oral): 3.72 g/kg
LD50 (guinea pig, oral): 1.41 g/kg
LD50 (mouse, oral): 0.85 g/kg
LD50 (mouse, SC): 0.82 g/kg
LD50 (rabbit, oral): 1.62 g/kg
LD50 (rat, oral): 1.41 g/kg

신진 대사

Maltol is rapidly and extensively metabolized in the dog and excreted by the conjugation pathway common to phenolic compounds. Rennhard (1971) reported that 57% of an iv dose was recovered in 24 hr, 88% of the total excretion occurring in the first 6 hr and 65-70% of the dose administered being recovered as sulphate and glucuronide conjugates

저장

Maltol solutions may be stored in glass or plastic containers. The bulk material should be stored in a well-closed container, protected from light, in a cool, dry place.

Purification Methods

It crystallises from CHCl3, toluene, aqueous 50% EtOH or H2O, and is volatile in steam. It can be readily sublimed in a vacuum. It forms a Cu2+ complex. [Beilstein 17 III/IV 5916, 18/1 V 114.]

비 호환성

Concentrated solutions in metal containers, including some grades of stainless steel, may discolor on storage.

Regulatory Status

GRAS listed. Included in the FDA Inactive Ingredients Database (oral solutions and syrups). Included in the Canadian List of Acceptable Non-medicinal Ingredients.

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원자재

준비 용품


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