헥사민

헥사민
헥사민 구조식 이미지
카스 번호:
100-97-0
한글명:
헥사민
동의어(한글):
헥사메틸렌테트라민;헥사민;헥사메틸렌테트라아민;메텐아민
상품명:
Hexamethylenetetramine
동의어(영문):
HMTA;HEXAMINE;METHENAMINE;UROTROPINE;1,3,5,7-TETRAAZAADAMANTANE;UROTROPIN;hexamethylentetramine;WLTP;Hexamethylenetetraamine;Hexamin
CBNumber:
CB8852597
분자식:
C6H12N4
포뮬러 무게:
140.19
MOL 파일:
100-97-0.mol

헥사민 속성

녹는점
280 °C (subl.) (lit.)
끓는 점
246.7°C (rough estimate)
밀도
1.33
증기 밀도
4.9 (vs air)
증기압
<0.01 mm Hg ( 20 °C)
굴절률
1.4260 (estimate)
인화점
482 °F
저장 조건
Store below +30°C.
용해도
H2O: 1 M at 20 °C, clear, colorless
물리적 상태
Solid
산도 계수 (pKa)
5.1(at 25℃)
색상
white
냄새
Odorless
수소이온지수(pH)
7-10 (100g/l, H2O, 20℃)
수용성
895 g/L (20 ºC)
감도
Hygroscopic
Merck
14,5966
승화점
263-295 ºC
BRN
2018
안정성
Stable. Incompatible with strong acids, strong oxidizing agents.
LogP
-2.18--2 at 20℃
CAS 데이터베이스
100-97-0(CAS DataBase Reference)
NIST
Hexamethylenetetramine(100-97-0)
EPA
Hexamethylenetetramine (100-97-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F,Xn,Xi
위험 카페고리 넘버 11-42/43-43
안전지침서 16-22-24-37
유엔번호(UN No.) UN 1328 4.1/PG 3
WGK 독일 1
RTECS 번호 MN4725000
F 고인화성물질 9-23
자연 발화 온도 770 °F
TSCA Yes
HS 번호 2933 69 40
위험 등급 4.1
포장분류 III
유해 물질 데이터 100-97-0(Hazardous Substances Data)
독성 LD50 orally in Rabbit: 9200 mg/kg
기존화학 물질 KE-18615
사고대비 물질 필터링 60
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H228 인화성 고체 인화성 고체 구분 1
구분 2
위험
경고
GHS hazard pictograms P210, P240,P241, P280, P370+P378
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P240 용기와 수용설비를 접지 및 접합시키시오.
P241 폭발 방지용 장비[전기적/환기/조명/...]을(를) 사용하시오.
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
NFPA 704
2
2 0

헥사민 C화학적 특성, 용도, 생산

개요

Hexamethylenetetramine is a hardener in epoxy resins of the bisphenol A type and can also be used as an anticorrosive agent. It is a sensitizing agent in ceramics workers.

화학적 성질

White or almost white, crystalline powder or colourless crystals.

용도

Hexamethylenetetramine is a versatile reagent in organic synthesis. It is used in the Duff reaction, the Sommelet reaction, and in the Delepine reaction.

정의

ChEBI: A polycyclic cage that is adamantane in which the carbon atoms at positions 1, 3, 5 and 7 are replaced by nitrogen atoms.

제조 방법

Hexamethylenetetramine (also known as hexamine, hexa or HMT) is prepared from ammonia and formaldehyde:

100-97-0 synthesis


Ammonia is passed into formalin at 20-30??C, with agitation. The resulting solution is evaporated under reduced pressure until most of the water is removed and the hexamethylenetetramine crystallizes. Yields of about 95% on both ammonia and formaldehyde can be achieved. Hexamethylenetetramine is a colourless crystalline solid which, on heating, sublimes with decomposition.

일반 설명

Odorless white crystalline powder or colorless lustrous crystals. Sublimes in a vacuum at about 505° F with some decomposition. Solutions are strong bases (pH of 0.2 molar aqueous solution is 8.4).

공기와 물의 반응

Highly flammable. Burns readily on contact with a flame with a smokeless flame. Finely powdered dust is significant dust explosion hazard. Water soluble.

반응 프로필

Hexamethylenetetramine is hygroscopic. Hexamethylenetetramine is sensitive to exposure to heat. Hexamethylenetetramine is incompatible with oxidizing agents. Hexamethylenetetramine is also incompatible with acids. Hexamethylenetetramine reacts violently with sodium peroxide. Hexamethylenetetramine reacts explosively with 1-bromopentaborane(9) at temperatures above 194° F. The complex with iodine deflagrates at 280° F. The 1:1 addition complex with iodoform has exploded at 352° F. Hexamethylenetetramine is corrosive to some metals, such as aluminum and zinc . Special Hazards of Combustion Products: Formaldehyde gas and ammonia may be given off when hot [USCG, 1999].

위험도

Skin irritant. Flammable, dangerous fire risk.

화재위험

Special Hazards of Combustion Products: Formaldehyde gas and ammonia may be given off when hot.

색상 색인 번호

Hexamethylenetetramine is used in the foundry, tire and rubber, and phenol formaldehyde resins industries and in other applications such as a hardener in epoxy resins Bisphenol A type and as an anticorrosive agent. It is an ammonia and formaldehyde releaser sometimes used in topical medicaments and cosmetics

Clinical Use

A venerable drug used for the disinfection of acidic urine, methenamine is a low-molecular-weight polymer of ammonia and formaldehyde that reverts to its components under mildly acidic conditions. Formaldehyde is the active antimicrobial component. Methenamine is used for recurrent urinary tract infections. The drug is available in various dosage forms as well as various salts, including the hippurate and mandelate.

Carcinogenicity

No significantly increased incidence of tumors was observed in rats or mice given HMTA for their lifetimes. Exposures in rats included 400 mg/day for 1 year, 10,000 ppm in drinking water for 2 years in each of three generations, 10,000 ppm in water for a lifetime (261), and up to 1000 ppm in the diet for 2 years. In mice, testing conditions included up to 10,000 ppm in drinking water for 60 weeks or 50,000 ppm for 30 weeks and a lifetime holding period, and up to 10,000 ppm in the diet for 2 years.
Injection of 25–30 g subcutaneously per mouse led to an increase in subcutaneous sarcomas in two experiments (418, 419) but not in two other studies. The relevance of this methodology to the workplace condition is questionable.

Purification Methods

It is soluble in H2O (67%), CHCl3 (10%), EtOH (8%) and Et2O (0.3%), and a 0.2M solution has a pH of 8.4. Dissolve it in hot absolute EtOH (reflux, Norit), filter using a heated funnel, cool at room temperature first, then in ice. Wash the crystals with cold Et2O, dry them in air or under a vacuum. A further crop can be obtained by adding Et2O to the filtrate. It sublimes above 260o without melting. The picrate has m 179o(dec). [pK2 0 4.85: Reilley & Schmid Anal Chem 30 947 1958, pK2 0 6.30: Pummerer & Hofmann Chem Ber 56 1255 1923.] [Beilstein 26 I 306, 26 II 200, 26 III/IV 1680.]

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