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L(+)-아라비노스

L-Arabinose

HCID 439195
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
5328-37-0
표준 SMILES
OC1OC[C@H](O)[C@H](O)[C@H]1O
InChIKey
SRBFZHDQGSBBOR-HWQSCIPKSA-N
분자식
C5H10O5
평균 분자량
150.13 g/mol

개요

L-arabinopyranose is the six-membered ring form of L-arabinose. It has a role as a mouse metabolite and an Escherichia coli metabolite.

이름 및 식별자

우선 이름
L-Arabinose
IUPAC
(3R,4S,5S)-oxane-2,3,4,5-tetrol
현지명
L(+)-아라비노스
영어명
L-Arabinose
분자식
C5H10O5
분자량
150.13

이름 및 동의어

L-ARABINOPYRANOSEarabinopyranosideL-ArabinopyranosideL-AraArabinopyranoseArabinose l-SNFG:AraAra (SNFG)RefChem:53263GlyTouCan:G88980IRDTXCID7019733CHEBI:30849
이름 더 보기
L(+)-아라비노스Amidosulfonic acidX-GAL (SOLID POWDERFEMA 3255pectinoseL- pentosePECTIN SUGARL(+)ArabinoseL(+)-ArbinoseL(+)-Gum sugar
ARAG88980IR226-214-65328-37-0ArabinoseArabinose, L-B40ROO395ZDTXSID9039733

데이터베이스 식별자

CAS
5328-37-0、87-72-9
PubChem CID
439195
ChEMBL
CHEMBL1357418、CHEMBL505348
ChEBI
CHEBI:17535
EC Number
201-767-6、226-214-6
Nikkaji
J192.647K

물성

구조 계산 물성

XLogP
-2.5
극성 표면적
90.2 Ų
수소 결합 공여자 수
4
수소 결합 수용자 수
5
회전 가능 결합 수
0
무거운 원자 수
10
형식 전하
0
복잡도
117

실험 및 물리화학적 성질

Chemical Classes · 2건

Biological Agents -> Monosaccharides and Derivatives

Biological Agents -> Monosaccharides and Derivatives

CosmeticsCosmetic ingredients (Arabinose) -> CIR (Cosmetic Ingredient Review)
LogP-3.02
Food AdditivesFLAVOR ENHANCER, FLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Physical Description · 2건

Colorless solid; [Merck Index]

White odorless powder; [Alfa Aesar MSDS]

Collision Cross Section · 2건

141.86 Ų [M+Na]+ [CCS Type: DT; Method: stepped-field]

134.6 Ų [M+Na]+ [CCS Type: DT; Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]

물리화학적 성질

녹는점
160 · 160-163 °C(lit.)
끓는 점
415.5 · 415.5±38.0 °C(Predicted)
밀도
1.508 · 1.508±0.06 g/cm3(Predicted)
증기압
0 Pa · 0Pa at 20℃
굴절률
104 ° · 104 ° (C=10, H2O)

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 6건

This chemical does not meet GHS hazard criteria for 99.6% (227 of 228) of all reports.

Not Classified

Aggregated GHS information provided per 228 reports by companies from 2 notifications to the ECHA C&L Inventory.

This chemical does not meet GHS hazard criteria for 100% (6 of 6) of all reports.

Not Classified

Aggregated GHS information provided per 6 reports by companies from 1 notifications to the ECHA C&L Inventory.

유해성 정보

Regulatory Information · 5건

Chemical: L-Arabinopyranose

Chemical: L-Arabinose

Status: Active Update: 13-11-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/25105

L-Arabinose: Does not have an individual approval but may be used under an appropriate group standard

L-Arabinopyranose: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

Other Safety Information · 2건

IMAP assessments - L-Arabinose: Environment tier I assessment

IMAP assessments - L-Arabinopyranose: Environment tier I assessment

Hazards Summary · 2건

May cause irritation; [Sigma-Aldrich MSDS]

May cause eye irritation; [Alfa Aesar MSDS]

Hazard Classes and Categories · 2건

Not Classified

Not Classified

독성 정보

Toxicity SummarySafe in the present practices of use and concentration. Ingredient, concentration, and use information are available in documents discoverable at https://cir-reports.cir-safety.org

화학 및 산업

용도 및 제조

Uses · 2건

CIR ingredient: Arabinose

Monosaccharide; The L-form is found in plants and mycobacteria; Used as a nutrient in bacterial culture media; [Merck Index] Used as a flavoring agent; [FDA]

General Manufacturing Information · 2건

L-Arabinopyranose: ACTIVE

L-Arabinose: ACTIVE

응용 분야 · 3건

개요L-Arabinose is considered a rare sugar that can be found naturally within the structures of most fruits and vegetables. Due to its low caloric sweetening effects, arabinose is commonly used in nutritional supplements and prescription drugs. In addition to its sweetening effects, when reacted with amino acid blends, using the Maillard Reaction, arabinose is able to contribute to the production of savory and meaty flavors used within the food and flavor industry.L-Arabinose is commonly used in the Flavor Industry to produce meaty or cooked/roasted flavors.

출처For biosynthetic reasons, most saccharides are almost always more abundant in nature as the "D"-form, or structurally analogous to D-glyceraldehyde. However, L-arabinose is in fact more common than D-arabinose in nature and is found in nature as a component of biopolymers such as hemicellulose and pectin. L-Arabinose is widely distributed in nature including Acacia and Larix species as a complex polysaccharide.

용도The L-arabinose operon, also known as the araBAD operon, has been the subject of much biomolecular research. The operon directs the catabolism of arabinose in E. coli, and it is dynamically activated in the presence of arabinose and the absence of glucose. In synthetic biology, arabinose is often used as a one-way or reversible switch for protein expression under the Pbad promoter in E. coli. This on-switch can be negated by the presence of glucose or reversed off by the addition of glucose in the culture medium which is a form of catabolite repression. L-Arabinose is an arabinose isomer widely found in nature, while D-arabinose is less common. L-Arabinose is a constituent of many biopolymers that make up plant cell walls. This monosaccharide is often used in cell culture media, serving as a bacterial carbon source, and can be used to distinguish between bacteria based on their fermentation abilities. L-Arabinose, in the absence of glucose, induces transcription of the ara operon in E. coli that encodes L-arabinose catabolizing enzymes. It does this by binding to the AraC protein and activating the PBAD promoter. The PBAD promoter is used in plasmid vectors as a switch for protein expression that can be turned on by L-arabinose or turned off by addition of glucose.

관련 반응

0건
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화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
FEMA
3255 · 3255 | L-ARABINOSE
저장 조건
room temp
용해도
2 O: · H2O: 1 M at 20 °C, 투명, 무색
산도 계수 (pKa)
12.46 · 12.46±0.20(Predicted)
물리적 상태
고체
색상
백색 결정체
수소이온지수(pH)
6.5 · 6.5-7.0 (100g/l, H2O, 20℃)
냄새
냄새 없는
수용성
거의 투명함
Merck
14 · 14,761
BRN
1723085 · 1723085
안정성
안정적인. 강한 산화제와 호환되지 않습니다.
InChI
1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1
InChIKey
PYMYPHUHKUWMLA-VAYJURFESA-N
SMILES
OC[C@H](O)[C@H](O)[C@@H](O)C=O
LogP
-2.8 at · -2.8 at 20℃
EPA
L-Arabinose (5328-37-0)
화학적 성질 · 1건

L-Arabinose is a white crystalline powder, It is a rare type of C5-sugar that naturally occurs in the hemicelluloses structure of most fruits and vegetables. Its name is derived from gum Arabic, another well-known food ingredient. Humans have always consumed L-Arabinose both pure as well as part of the hemicelluloses structure. The highest concentrations of L-Arabinose in food as monosaccharide can be found in instant coffee, wine and sake.

안전 데이터

wgk
3
tsca
TSCA listed
HS 번호
2940 00 00
기존화학 물질
2015-3-7163
F 고인화성물질
3-10
스토리지 클래스
11 - Combustible Solids

제조 방법

By partial hydrolysis of mesquite gum.

상·하류 제품 정보

상류 원료

엘라그산3,7,8-tri-O-methylellagic acidalpha-L-Rhamnose말토덱스트린D-갈락토오스

하류 제품

3-O-메틸엘라그산D-엑실로즈L-erythro-2-Pentulose (9CI)L-아라비노스히드라존

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추가 설명

정의l-enantiomers occur naturally. lArabinose is common in vegetable gums, especially arabic.